---
_id: '10841'
abstract:
- lang: eng
  text: In eukaryotes, clathrin-coated vesicles (CCVs) facilitate the internalization
    of material from the cell surface as well as the movement of cargo in post-Golgi
    trafficking pathways. This diversity of functions is partially provided by multiple
    monomeric and multimeric clathrin adaptor complexes that provide compartment and
    cargo selectivity. The adaptor-protein assembly polypeptide-1 (AP-1) complex operates
    as part of the secretory pathway at the trans-Golgi network (TGN), while the AP-2
    complex and the TPLATE complex jointly operate at the plasma membrane to execute
    clathrin-mediated endocytosis. Key to our further understanding of clathrin-mediated
    trafficking in plants will be the comprehensive identification and characterization
    of the network of evolutionarily conserved and plant-specific core and accessory
    machinery involved in the formation and targeting of CCVs. To facilitate these
    studies, we have analyzed the proteome of enriched TGN/early endosome-derived
    and endocytic CCVs isolated from dividing and expanding suspension-cultured Arabidopsis
    (Arabidopsis thaliana) cells. Tandem mass spectrometry analysis results were validated
    by differential chemical labeling experiments to identify proteins co-enriching
    with CCVs. Proteins enriched in CCVs included previously characterized CCV components
    and cargos such as the vacuolar sorting receptors in addition to conserved and
    plant-specific components whose function in clathrin-mediated trafficking has
    not been previously defined. Notably, in addition to AP-1 and AP-2, all subunits
    of the AP-4 complex, but not AP-3 or AP-5, were found to be in high abundance
    in the CCV proteome. The association of AP-4 with suspension-cultured Arabidopsis
    CCVs is further supported via additional biochemical data.
acknowledged_ssus:
- _id: EM-Fac
acknowledgement: 'The authors would like to acknowledge the VIB Proteomics Core Facility
  (VIB-UGent Center for Medical Biotechnology in Ghent, Belgium) and the Research
  Technology Support Facility Proteomics Core (Michigan State University in East Lansing,
  Michigan) for sample analysis, as well as the University of Wisconsin Biotechnology
  Center Mass Spectrometry Core Facility (Madison, WI) for help with data processing.
  Additionally, we are grateful to Sue Weintraub (UT Health San Antonio) and Sydney
  Thomas (UW- Madison) for assistance with data analysis. This research was supported
  by grants to S.Y.B. from the National Science Foundation (Nos. 1121998 and 1614915)
  and a Vilas Associate Award (University of Wisconsin, Madison, Graduate School);
  to J.P. from the National Natural Science Foundation of China (Nos. 91754104, 31820103008,
  and 31670283); to I.H. from the National Research Foundation of Korea (No. 2019R1A2B5B03099982).
  This research was also supported by the Scientific Service Units (SSU) of IST Austria
  through resources provided by the Electron microscopy Facility (EMF). A.J. is supported
  by funding from the Austrian Science Fund (FWF): I3630B25 to J.F. A.H. is supported
  by funding from the National Science Foundation (NSF IOS Nos. 1025837 and 1147032).'
article_processing_charge: No
article_type: original
author:
- first_name: DA
  full_name: Dahhan, DA
  last_name: Dahhan
- first_name: GD
  full_name: Reynolds, GD
  last_name: Reynolds
- first_name: JJ
  full_name: Cárdenas, JJ
  last_name: Cárdenas
- first_name: D
  full_name: Eeckhout, D
  last_name: Eeckhout
- first_name: Alexander J
  full_name: Johnson, Alexander J
  id: 46A62C3A-F248-11E8-B48F-1D18A9856A87
  last_name: Johnson
  orcid: 0000-0002-2739-8843
- first_name: K
  full_name: Yperman, K
  last_name: Yperman
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: N
  full_name: Vang, N
  last_name: Vang
- first_name: X
  full_name: Yan, X
  last_name: Yan
- first_name: I
  full_name: Hwang, I
  last_name: Hwang
- first_name: A
  full_name: Heese, A
  last_name: Heese
- first_name: G
  full_name: De Jaeger, G
  last_name: De Jaeger
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: D
  full_name: Van Damme, D
  last_name: Van Damme
- first_name: J
  full_name: Pan, J
  last_name: Pan
- first_name: SY
  full_name: Bednarek, SY
  last_name: Bednarek
citation:
  ama: Dahhan D, Reynolds G, Cárdenas J, et al. Proteomic characterization of isolated
    Arabidopsis clathrin-coated vesicles reveals evolutionarily conserved and plant-specific
    components. <i>Plant Cell</i>. 2022;34(6):2150-2173. doi:<a href="https://doi.org/10.1093/plcell/koac071">10.1093/plcell/koac071</a>
  apa: Dahhan, D., Reynolds, G., Cárdenas, J., Eeckhout, D., Johnson, A. J., Yperman,
    K., … Bednarek, S. (2022). Proteomic characterization of isolated Arabidopsis
    clathrin-coated vesicles reveals evolutionarily conserved and plant-specific components.
    <i>Plant Cell</i>. Oxford Academic. <a href="https://doi.org/10.1093/plcell/koac071">https://doi.org/10.1093/plcell/koac071</a>
  chicago: Dahhan, DA, GD Reynolds, JJ Cárdenas, D Eeckhout, Alexander J Johnson,
    K Yperman, Walter Kaufmann, et al. “Proteomic Characterization of Isolated Arabidopsis
    Clathrin-Coated Vesicles Reveals Evolutionarily Conserved and Plant-Specific Components.”
    <i>Plant Cell</i>. Oxford Academic, 2022. <a href="https://doi.org/10.1093/plcell/koac071">https://doi.org/10.1093/plcell/koac071</a>.
  ieee: D. Dahhan <i>et al.</i>, “Proteomic characterization of isolated Arabidopsis
    clathrin-coated vesicles reveals evolutionarily conserved and plant-specific components,”
    <i>Plant Cell</i>, vol. 34, no. 6. Oxford Academic, pp. 2150–2173, 2022.
  ista: Dahhan D, Reynolds G, Cárdenas J, Eeckhout D, Johnson AJ, Yperman K, Kaufmann
    W, Vang N, Yan X, Hwang I, Heese A, De Jaeger G, Friml J, Van Damme D, Pan J,
    Bednarek S. 2022. Proteomic characterization of isolated Arabidopsis clathrin-coated
    vesicles reveals evolutionarily conserved and plant-specific components. Plant
    Cell. 34(6), 2150–2173.
  mla: Dahhan, DA, et al. “Proteomic Characterization of Isolated Arabidopsis Clathrin-Coated
    Vesicles Reveals Evolutionarily Conserved and Plant-Specific Components.” <i>Plant
    Cell</i>, vol. 34, no. 6, Oxford Academic, 2022, pp. 2150–73, doi:<a href="https://doi.org/10.1093/plcell/koac071">10.1093/plcell/koac071</a>.
  short: D. Dahhan, G. Reynolds, J. Cárdenas, D. Eeckhout, A.J. Johnson, K. Yperman,
    W. Kaufmann, N. Vang, X. Yan, I. Hwang, A. Heese, G. De Jaeger, J. Friml, D. Van
    Damme, J. Pan, S. Bednarek, Plant Cell 34 (2022) 2150–2173.
date_created: 2022-03-08T13:47:51Z
date_published: 2022-06-01T00:00:00Z
date_updated: 2023-08-02T14:46:48Z
day: '01'
department:
- _id: JiFr
- _id: EM-Fac
doi: 10.1093/plcell/koac071
external_id:
  isi:
  - '000767438800001'
  pmid:
  - '35218346'
intvolume: '        34'
isi: 1
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/2021.09.16.460678
month: '06'
oa: 1
oa_version: Preprint
page: 2150-2173
pmid: 1
project:
- _id: 26538374-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I03630
  name: Molecular mechanisms of endocytic cargo recognition in plants
publication: Plant Cell
publication_identifier:
  eissn:
  - 1532-298x
  issn:
  - 1040-4651
publication_status: published
publisher: Oxford Academic
quality_controlled: '1'
scopus_import: '1'
status: public
title: Proteomic characterization of isolated Arabidopsis clathrin-coated vesicles
  reveals evolutionarily conserved and plant-specific components
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 34
year: '2022'
...
---
_id: '10888'
abstract:
- lang: eng
  text: Despite the growing interest in using chemical genetics in plant research,
    small molecule target identification remains a major challenge. The cellular thermal
    shift assay coupled with high-resolution mass spectrometry (CETSA MS) that monitors
    changes in the thermal stability of proteins caused by their interactions with
    small molecules, other proteins, or posttranslational modifications, allows the
    discovery of drug targets or the study of protein–metabolite and protein–protein
    interactions mainly in mammalian cells. To showcase the applicability of this
    method in plants, we applied CETSA MS to intact Arabidopsis thaliana cells and
    identified the thermal proteome of the plant-specific glycogen synthase kinase
    3 (GSK3) inhibitor, bikinin. A comparison between the thermal and the phosphoproteomes
    of bikinin revealed the auxin efflux carrier PIN-FORMED1 (PIN1) as a substrate
    of the Arabidopsis GSK3s that negatively regulate the brassinosteroid signaling.
    We established that PIN1 phosphorylation by the GSK3s is essential for maintaining
    its intracellular polarity that is required for auxin-mediated regulation of vascular
    patterning in the leaf, thus revealing cross-talk between brassinosteroid and
    auxin signaling.
acknowledgement: "We thank Yanhai Yin for providing the anti-BES1 antibody, Johan
  Winne and Brenda Callebaut for synthesizing bikinin, Yuki Kondo and Hiroo Fukuda
  for published materials, Tomasz Nodzy\x03nski for useful advice, and Martine De
  Cock for help in preparing the manuscript. This\r\nwork was supported by the China
  Scholarship Council for predoctoral (Q.L. and X.X.) and postdoctoral (Y.Z.) fellowships;
  the Agency for Innovation by Science and Technology for a predoctoral fellowship
  (W.D.); the Research Foundation-Flanders, Projects G009018N and G002121N (E.R.);
  and the VIB TechWatch Fund (E.R.)."
article_number: e2118220119
article_processing_charge: No
article_type: original
author:
- first_name: Qing
  full_name: Lu, Qing
  last_name: Lu
- first_name: Yonghong
  full_name: Zhang, Yonghong
  last_name: Zhang
- first_name: Joakim
  full_name: Hellner, Joakim
  last_name: Hellner
- first_name: Caterina
  full_name: Giannini, Caterina
  id: e3fdddd5-f6e0-11ea-865d-ca99ee6367f4
  last_name: Giannini
- first_name: Xiangyu
  full_name: Xu, Xiangyu
  last_name: Xu
- first_name: Jarne
  full_name: Pauwels, Jarne
  last_name: Pauwels
- first_name: Qian
  full_name: Ma, Qian
  last_name: Ma
- first_name: Wim
  full_name: Dejonghe, Wim
  last_name: Dejonghe
- first_name: Huibin
  full_name: Han, Huibin
  id: 31435098-F248-11E8-B48F-1D18A9856A87
  last_name: Han
- first_name: Brigitte
  full_name: Van De Cotte, Brigitte
  last_name: Van De Cotte
- first_name: Francis
  full_name: Impens, Francis
  last_name: Impens
- first_name: Kris
  full_name: Gevaert, Kris
  last_name: Gevaert
- first_name: Ive
  full_name: De Smet, Ive
  last_name: De Smet
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Daniel Martinez
  full_name: Molina, Daniel Martinez
  last_name: Molina
- first_name: Eugenia
  full_name: Russinova, Eugenia
  last_name: Russinova
citation:
  ama: Lu Q, Zhang Y, Hellner J, et al. Proteome-wide cellular thermal shift assay
    reveals unexpected cross-talk between brassinosteroid and auxin signaling. <i>Proceedings
    of the National Academy of Sciences of the United States of America</i>. 2022;119(11).
    doi:<a href="https://doi.org/10.1073/pnas.2118220119">10.1073/pnas.2118220119</a>
  apa: Lu, Q., Zhang, Y., Hellner, J., Giannini, C., Xu, X., Pauwels, J., … Russinova,
    E. (2022). Proteome-wide cellular thermal shift assay reveals unexpected cross-talk
    between brassinosteroid and auxin signaling. <i>Proceedings of the National Academy
    of Sciences of the United States of America</i>. Proceedings of the National Academy
    of Sciences. <a href="https://doi.org/10.1073/pnas.2118220119">https://doi.org/10.1073/pnas.2118220119</a>
  chicago: Lu, Qing, Yonghong Zhang, Joakim Hellner, Caterina Giannini, Xiangyu Xu,
    Jarne Pauwels, Qian Ma, et al. “Proteome-Wide Cellular Thermal Shift Assay Reveals Unexpected
    Cross-Talk between Brassinosteroid and Auxin Signaling.” <i>Proceedings of the
    National Academy of Sciences of the United States of America</i>. Proceedings
    of the National Academy of Sciences, 2022. <a href="https://doi.org/10.1073/pnas.2118220119">https://doi.org/10.1073/pnas.2118220119</a>.
  ieee: Q. Lu <i>et al.</i>, “Proteome-wide cellular thermal shift assay reveals unexpected
    cross-talk between brassinosteroid and auxin signaling,” <i>Proceedings of the
    National Academy of Sciences of the United States of America</i>, vol. 119, no.
    11. Proceedings of the National Academy of Sciences, 2022.
  ista: Lu Q, Zhang Y, Hellner J, Giannini C, Xu X, Pauwels J, Ma Q, Dejonghe W, Han
    H, Van De Cotte B, Impens F, Gevaert K, De Smet I, Friml J, Molina DM, Russinova
    E. 2022. Proteome-wide cellular thermal shift assay reveals unexpected cross-talk
    between brassinosteroid and auxin signaling. Proceedings of the National Academy
    of Sciences of the United States of America. 119(11), e2118220119.
  mla: Lu, Qing, et al. “Proteome-Wide Cellular Thermal Shift Assay Reveals Unexpected
    Cross-Talk between Brassinosteroid and Auxin Signaling.” <i>Proceedings of the
    National Academy of Sciences of the United States of America</i>, vol. 119, no.
    11, e2118220119, Proceedings of the National Academy of Sciences, 2022, doi:<a
    href="https://doi.org/10.1073/pnas.2118220119">10.1073/pnas.2118220119</a>.
  short: Q. Lu, Y. Zhang, J. Hellner, C. Giannini, X. Xu, J. Pauwels, Q. Ma, W. Dejonghe,
    H. Han, B. Van De Cotte, F. Impens, K. Gevaert, I. De Smet, J. Friml, D.M. Molina,
    E. Russinova, Proceedings of the National Academy of Sciences of the United States
    of America 119 (2022).
date_created: 2022-03-20T23:01:39Z
date_published: 2022-03-07T00:00:00Z
date_updated: 2023-08-03T06:06:27Z
day: '07'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1073/pnas.2118220119
external_id:
  isi:
  - '000771756300008'
  pmid:
  - '35254915'
file:
- access_level: open_access
  checksum: 83e0fea7919570d0b519b41193342571
  content_type: application/pdf
  creator: dernst
  date_created: 2022-03-21T09:19:47Z
  date_updated: 2022-03-21T09:19:47Z
  file_id: '10910'
  file_name: 2022_PNAS_Lu.pdf
  file_size: 2169534
  relation: main_file
  success: 1
file_date_updated: 2022-03-21T09:19:47Z
has_accepted_license: '1'
intvolume: '       119'
isi: 1
issue: '11'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
publication: Proceedings of the National Academy of Sciences of the United States
  of America
publication_identifier:
  eissn:
  - 1091-6490
publication_status: published
publisher: Proceedings of the National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Proteome-wide cellular thermal shift assay reveals unexpected cross-talk between
  brassinosteroid and auxin signaling
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 119
year: '2022'
...
---
_id: '11489'
abstract:
- lang: eng
  text: Much of plant development depends on cell-to-cell redistribution of the plant
    hormone auxin, which is facilitated by the plasma membrane (PM) localized PIN
    FORMED (PIN) proteins. Auxin export activity, developmental roles, subcellular
    trafficking, and polarity of PINs have been well studied, but their structure
    remains elusive besides a rough outline that they contain two groups of 5 alpha-helices
    connected by a large hydrophilic loop (HL). Here, we focus on the PIN1 HL as we
    could produce it in sufficient quantities for biochemical investigations to provide
    insights into its secondary structure. Circular dichroism (CD) studies revealed
    its nature as an intrinsically disordered protein (IDP), manifested by the increase
    of structure content upon thermal melting. Consistent with IDPs serving as interaction
    platforms, PIN1 loops homodimerize. PIN1 HL cytoplasmic overexpression in Arabidopsis
    disrupts early endocytic trafficking of PIN1 and PIN2 and causes defects in the
    cotyledon vasculature formation. In summary, we demonstrate that PIN1 HL has an
    intrinsically disordered nature, which must be considered to gain further structural
    insights. Some secondary structures may form transiently during pairing with known
    and yet-to-be-discovered interactors.
acknowledgement: 'We thank Charo del Genio from Coventry University and Richard Napier
  from the University of Warwick for helpful discussion concerning protein modeling
  and inspiration concerning CD spectroscopy, respectively. We thank Jan Hejatko for
  sharing the published AHP2 construct. We also thank Josef Houser from the core facility
  BIC CEITEC for valuable assistance, discussions, and ideas relating to CD. We acknowledge
  the: Core Facility CELLIM of CEITEC supported by the Czech-BioImaging large RI project
  (LM2018129 funded by MEYS CR), part of the Euro-BioImaging (www.eurobioimaging.eu
  accessed on 1 January 2016) ALM and medical imaging Node (Brno, CZ), CF Biomolecular
  Interactions and Crystallization of CIISB, Instruct-CZ Centre, supported by MEYS
  CR (LM2018127) and European Regional Development Fund-Project “UP CIISB“ (No. CZ.02.1.01/0.0/0.0/18_046/0015974)
  for their support with obtaining scientific data presented in this paper; Plant
  Sciences Core Facility of CEITEC Masaryk University for technical support. Open
  Access Funding by the Austrian Science Fund (FWF).'
article_processing_charge: Yes
article_type: original
author:
- first_name: V
  full_name: Bilanovičová, V
  last_name: Bilanovičová
- first_name: N
  full_name: Rýdza, N
  last_name: Rýdza
- first_name: L
  full_name: Koczka, L
  last_name: Koczka
- first_name: M
  full_name: Hess, M
  last_name: Hess
- first_name: E
  full_name: Feraru, E
  last_name: Feraru
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: T
  full_name: Nodzyński, T
  last_name: Nodzyński
citation:
  ama: Bilanovičová V, Rýdza N, Koczka L, et al. The hydrophilic loop of Arabidopsis
    PIN1 auxin efflux carrier harbors hallmarks of an intrinsically disordered protein.
    <i>International Journal of Molecular Sciences</i>. 2022;23(11):6352. doi:<a href="https://doi.org/10.3390/ijms23116352">10.3390/ijms23116352</a>
  apa: Bilanovičová, V., Rýdza, N., Koczka, L., Hess, M., Feraru, E., Friml, J., &#38;
    Nodzyński, T. (2022). The hydrophilic loop of Arabidopsis PIN1 auxin efflux carrier
    harbors hallmarks of an intrinsically disordered protein. <i>International Journal
    of Molecular Sciences</i>. MDPI. <a href="https://doi.org/10.3390/ijms23116352">https://doi.org/10.3390/ijms23116352</a>
  chicago: Bilanovičová, V, N Rýdza, L Koczka, M Hess, E Feraru, Jiří Friml, and T
    Nodzyński. “The Hydrophilic Loop of Arabidopsis PIN1 Auxin Efflux Carrier Harbors
    Hallmarks of an Intrinsically Disordered Protein.” <i>International Journal of
    Molecular Sciences</i>. MDPI, 2022. <a href="https://doi.org/10.3390/ijms23116352">https://doi.org/10.3390/ijms23116352</a>.
  ieee: V. Bilanovičová <i>et al.</i>, “The hydrophilic loop of Arabidopsis PIN1 auxin
    efflux carrier harbors hallmarks of an intrinsically disordered protein,” <i>International
    Journal of Molecular Sciences</i>, vol. 23, no. 11. MDPI, p. 6352, 2022.
  ista: Bilanovičová V, Rýdza N, Koczka L, Hess M, Feraru E, Friml J, Nodzyński T.
    2022. The hydrophilic loop of Arabidopsis PIN1 auxin efflux carrier harbors hallmarks
    of an intrinsically disordered protein. International Journal of Molecular Sciences.
    23(11), 6352.
  mla: Bilanovičová, V., et al. “The Hydrophilic Loop of Arabidopsis PIN1 Auxin Efflux
    Carrier Harbors Hallmarks of an Intrinsically Disordered Protein.” <i>International
    Journal of Molecular Sciences</i>, vol. 23, no. 11, MDPI, 2022, p. 6352, doi:<a
    href="https://doi.org/10.3390/ijms23116352">10.3390/ijms23116352</a>.
  short: V. Bilanovičová, N. Rýdza, L. Koczka, M. Hess, E. Feraru, J. Friml, T. Nodzyński,
    International Journal of Molecular Sciences 23 (2022) 6352.
date_created: 2022-07-05T15:14:34Z
date_published: 2022-06-06T00:00:00Z
date_updated: 2023-08-09T10:13:57Z
day: '06'
ddc:
- '570'
department:
- _id: JiFr
doi: 10.3390/ijms23116352
external_id:
  isi:
  - '000808733300001'
  pmid:
  - '35683031'
file:
- access_level: open_access
  checksum: e997a57a928ec9d51fad8ce824a05935
  content_type: application/pdf
  creator: cchlebak
  date_created: 2022-07-06T07:36:59Z
  date_updated: 2022-07-06T07:36:59Z
  file_id: '11492'
  file_name: 2022_IntJMolSci_Bilanovicova.pdf
  file_size: 2324542
  relation: main_file
  success: 1
file_date_updated: 2022-07-06T07:36:59Z
has_accepted_license: '1'
intvolume: '        23'
isi: 1
issue: '11'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: '6352'
pmid: 1
project:
- _id: 262EF96E-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P29988
  name: RNA-directed DNA methylation in plant development
publication: International Journal of Molecular Sciences
publication_identifier:
  issn:
  - 1422-0067
publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: The hydrophilic loop of Arabidopsis PIN1 auxin efflux carrier harbors hallmarks
  of an intrinsically disordered protein
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 23
year: '2022'
...
---
_id: '11589'
abstract:
- lang: eng
  text: Calcium-dependent protein kinases (CPK) are key components of a wide array
    of signaling pathways, translating stress and nutrient signaling into the modulation
    of cellular processes such as ion transport and transcription. However, not much
    is known about CPKs in endomembrane trafficking. Here, we screened for CPKs that
    impact on root growth and gravitropism, by overexpressing constitutively active
    forms of CPKs under the control of an inducible promoter in Arabidopsis thaliana.
    We found that inducible overexpression of an constitutive active CPK30 (CA-CPK30)
    resulted in a loss of root gravitropism and ectopic auxin accumulation in the
    root tip. Immunolocalization revealed that CA-CPK30 roots have reduced PIN protein
    levels, PIN1 polarity defects and impaired Brefeldin A (BFA)-sensitive trafficking.
    Moreover, FM4-64 uptake was reduced, indicative of a defect in endocytosis. The
    effects on BFA-sensitive trafficking were not specific to PINs, as BFA could not
    induce aggregation of ARF1- and CHC-labeled endosomes in CA-CPK30. Interestingly,
    the interference with BFA-body formation, could be reverted by increasing the
    extracellular pH, indicating a pH-dependence of this CA-CPK30 effect. Altogether,
    our data reveal an important role for CPK30 in root growth regulation and endomembrane
    trafficking in Arabidopsis thaliana.
acknowledgement: "RW and JC predoctoral fellows that were supported by the Chinese
  Science Counsil. The IPS2 benefits from the support of the LabEx Saclay Plant Sciences-SPS
  (ANR-10-LABX-0040-SPS).\r\nWe thank Jen Sheen for establishing and generously sharing
  the CKP family clone sets, and for providing useful feedback on the manuscript."
article_number: '862398'
article_processing_charge: No
article_type: original
author:
- first_name: Ren
  full_name: Wang, Ren
  last_name: Wang
- first_name: Ellie
  full_name: Himschoot, Ellie
  last_name: Himschoot
- first_name: Jian
  full_name: Chen, Jian
  last_name: Chen
- first_name: Marie
  full_name: Boudsocq, Marie
  last_name: Boudsocq
- first_name: Danny
  full_name: Geelen, Danny
  last_name: Geelen
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
citation:
  ama: Wang R, Himschoot E, Chen J, et al. Constitutive active CPK30 interferes with
    root growth and endomembrane trafficking in Arabidopsis thaliana. <i>Frontiers
    in Plant Science</i>. 2022;13. doi:<a href="https://doi.org/10.3389/fpls.2022.862398">10.3389/fpls.2022.862398</a>
  apa: Wang, R., Himschoot, E., Chen, J., Boudsocq, M., Geelen, D., Friml, J., … Vanneste,
    S. (2022). Constitutive active CPK30 interferes with root growth and endomembrane
    trafficking in Arabidopsis thaliana. <i>Frontiers in Plant Science</i>. Frontiers.
    <a href="https://doi.org/10.3389/fpls.2022.862398">https://doi.org/10.3389/fpls.2022.862398</a>
  chicago: Wang, Ren, Ellie Himschoot, Jian Chen, Marie Boudsocq, Danny Geelen, Jiří
    Friml, Tom Beeckman, and Steffen Vanneste. “Constitutive Active CPK30 Interferes
    with Root Growth and Endomembrane Trafficking in Arabidopsis Thaliana.” <i>Frontiers
    in Plant Science</i>. Frontiers, 2022. <a href="https://doi.org/10.3389/fpls.2022.862398">https://doi.org/10.3389/fpls.2022.862398</a>.
  ieee: R. Wang <i>et al.</i>, “Constitutive active CPK30 interferes with root growth
    and endomembrane trafficking in Arabidopsis thaliana,” <i>Frontiers in Plant Science</i>,
    vol. 13. Frontiers, 2022.
  ista: Wang R, Himschoot E, Chen J, Boudsocq M, Geelen D, Friml J, Beeckman T, Vanneste
    S. 2022. Constitutive active CPK30 interferes with root growth and endomembrane
    trafficking in Arabidopsis thaliana. Frontiers in Plant Science. 13, 862398.
  mla: Wang, Ren, et al. “Constitutive Active CPK30 Interferes with Root Growth and
    Endomembrane Trafficking in Arabidopsis Thaliana.” <i>Frontiers in Plant Science</i>,
    vol. 13, 862398, Frontiers, 2022, doi:<a href="https://doi.org/10.3389/fpls.2022.862398">10.3389/fpls.2022.862398</a>.
  short: R. Wang, E. Himschoot, J. Chen, M. Boudsocq, D. Geelen, J. Friml, T. Beeckman,
    S. Vanneste, Frontiers in Plant Science 13 (2022).
date_created: 2022-07-17T22:01:54Z
date_published: 2022-06-16T00:00:00Z
date_updated: 2023-08-03T12:01:47Z
day: '16'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.3389/fpls.2022.862398
external_id:
  isi:
  - '000819250500001'
  pmid:
  - '35783951'
file:
- access_level: open_access
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  date_created: 2022-07-18T08:05:15Z
  date_updated: 2022-07-18T08:05:15Z
  file_id: '11596'
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  file_size: 5040638
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  success: 1
file_date_updated: 2022-07-18T08:05:15Z
has_accepted_license: '1'
intvolume: '        13'
isi: 1
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: Frontiers in Plant Science
publication_identifier:
  eissn:
  - 1664-462X
publication_status: published
publisher: Frontiers
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: https://doi.org/10.3389/fpls.2022.1100792
scopus_import: '1'
status: public
title: Constitutive active CPK30 interferes with root growth and endomembrane trafficking
  in Arabidopsis thaliana
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 13
year: '2022'
...
---
_id: '11626'
abstract:
- lang: eng
  text: Plant growth and development is well known to be both, flexible and dynamic.
    The high capacity for post-embryonic organ formation and tissue regeneration requires
    tightly regulated intercellular communication and coordinated tissue polarization.
    One of the most important drivers for patterning and polarity in plant development
    is the phytohormone auxin. Auxin has the unique characteristic to establish polarized
    channels for its own active directional cell to cell transport. This fascinating
    phenomenon is called auxin canalization. Those auxin transport channels are characterized
    by the expression and polar, subcellular localization of PIN auxin efflux carriers.
    PIN proteins have the ability to dynamically change their localization and auxin
    itself can affect this by interfering with trafficking. Most of the underlying
    molecular mechanisms of canalization still remain enigmatic. What is known so
    far is that canonical auxin signaling is indispensable but also other non-canonical
    signaling components are thought to play a role. In order to shed light into the
    mysteries auf auxin canalization this study revisits the branches of auxin signaling
    in detail. Further a new auxin analogue, PISA, is developed which triggers auxin-like
    responses but does not directly activate canonical transcriptional auxin signaling.
    We revisit the direct auxin effect on PIN trafficking where we found that, contradictory
    to previous observations, auxin is very specifically promoting endocytosis of
    PIN2 but has no overall effect on endocytosis. Further, we evaluate which cellular
    processes related to PIN subcellular dynamics are involved in the establishment
    of auxin conducting channels and the formation of vascular tissue. We are re-evaluating
    the function of AUXIN BINDING PROTEIN 1 (ABP1) and provide a comprehensive picture
    about its developmental phneotypes and involvement in auxin signaling and canalization.
    Lastly, we are focusing on the crosstalk between the hormone strigolactone (SL)
    and auxin and found that SL is interfering with essentially all processes involved
    in auxin canalization in a non-transcriptional manner. Lastly we identify a new
    way of SL perception and signaling which is emanating from mitochondria, is independent
    of canonical SL signaling and is modulating primary root growth.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Michelle C
  full_name: Gallei, Michelle C
  id: 35A03822-F248-11E8-B48F-1D18A9856A87
  last_name: Gallei
  orcid: 0000-0003-1286-7368
citation:
  ama: Gallei MC. Auxin and strigolactone non-canonical signaling regulating development
    in Arabidopsis thaliana. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11626">10.15479/at:ista:11626</a>
  apa: Gallei, M. C. (2022). <i>Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/at:ista:11626">https://doi.org/10.15479/at:ista:11626</a>
  chicago: Gallei, Michelle C. “Auxin and Strigolactone Non-Canonical Signaling Regulating
    Development in Arabidopsis Thaliana.” Institute of Science and Technology Austria,
    2022. <a href="https://doi.org/10.15479/at:ista:11626">https://doi.org/10.15479/at:ista:11626</a>.
  ieee: M. C. Gallei, “Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana,” Institute of Science and Technology Austria,
    2022.
  ista: Gallei MC. 2022. Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana. Institute of Science and Technology Austria.
  mla: Gallei, Michelle C. <i>Auxin and Strigolactone Non-Canonical Signaling Regulating
    Development in Arabidopsis Thaliana</i>. Institute of Science and Technology Austria,
    2022, doi:<a href="https://doi.org/10.15479/at:ista:11626">10.15479/at:ista:11626</a>.
  short: M.C. Gallei, Auxin and Strigolactone Non-Canonical Signaling Regulating Development
    in Arabidopsis Thaliana, Institute of Science and Technology Austria, 2022.
date_created: 2022-07-20T11:21:53Z
date_published: 2022-07-20T00:00:00Z
date_updated: 2024-10-29T10:22:45Z
day: '20'
ddc:
- '575'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JiFr
doi: 10.15479/at:ista:11626
ec_funded: 1
file:
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  checksum: bd7ac35403cf5b4b2607287d2a104b3a
  content_type: application/pdf
  creator: mgallei
  date_created: 2022-07-25T09:08:47Z
  date_updated: 2022-07-25T09:08:47Z
  file_id: '11645'
  file_name: Thesis_Gallei.pdf
  file_size: 9730864
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  creator: mgallei
  date_created: 2022-07-25T09:09:09Z
  date_updated: 2022-07-25T09:39:58Z
  file_id: '11646'
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  file_size: 19560720
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  creator: mgallei
  date_created: 2022-07-25T09:09:32Z
  date_updated: 2022-07-25T09:39:58Z
  description: This is the print version of the thesis including the full appendix
  file_id: '11647'
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  creator: mgallei
  date_created: 2022-07-25T11:48:45Z
  date_updated: 2022-07-25T11:48:45Z
  file_id: '11650'
  file_name: Thesis_Gallei_Appendix.pdf
  file_size: 15435966
  relation: main_file
file_date_updated: 2022-07-25T11:48:45Z
has_accepted_license: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: '248'
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '742985'
  name: Tracing Evolution of Auxin Transport and Polarity in Plants
publication_identifier:
  isbn:
  - 978-3-99078-019-0
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '9287'
    relation: part_of_dissertation
    status: public
  - id: '7142'
    relation: part_of_dissertation
    status: public
  - id: '7465'
    relation: part_of_dissertation
    status: public
  - id: '8138'
    relation: part_of_dissertation
    status: public
  - id: '6260'
    relation: part_of_dissertation
    status: public
  - id: '8931'
    relation: part_of_dissertation
    status: public
  - id: '10411'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Eilon
  full_name: Shani, Eilon
  last_name: Shani
title: Auxin and strigolactone non-canonical signaling regulating development in Arabidopsis
  thaliana
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2022'
...
---
_id: '11723'
abstract:
- lang: eng
  text: Plant cell growth responds rapidly to various stimuli, adapting architecture
    to environmental changes. Two major endogenous signals regulating growth are the
    phytohormone auxin and the secreted peptides rapid alkalinization factors (RALFs).
    Both trigger very rapid cellular responses and also exert long-term effects [Du
    et al., Annu. Rev. Plant Biol. 71, 379–402 (2020); Blackburn et al., Plant Physiol.
    182, 1657–1666 (2020)]. However, the way, in which these distinct signaling pathways
    converge to regulate growth, remains unknown. Here, using vertical confocal microscopy
    combined with a microfluidic chip, we addressed the mechanism of RALF action on
    growth. We observed correlation between RALF1-induced rapid Arabidopsis thaliana
    root growth inhibition and apoplast alkalinization during the initial phase of
    the response, and revealed that RALF1 reversibly inhibits primary root growth
    through apoplast alkalinization faster than within 1 min. This rapid apoplast
    alkalinization was the result of RALF1-induced net H+ influx and was mediated
    by the receptor FERONIA (FER). Furthermore, we investigated the cross-talk between
    RALF1 and the auxin signaling pathways during root growth regulation. The results
    showed that RALF-FER signaling triggered auxin signaling with a delay of approximately
    1 h by up-regulating auxin biosynthesis, thus contributing to sustained RALF1-induced
    growth inhibition. This biphasic RALF1 action on growth allows plants to respond
    rapidly to environmental stimuli and also reprogram growth and development in
    the long term.
acknowledgement: We thank Sarah M. Assmann, Kris Vissenberg, and Nadine Paris for
  kindly sharing seeds; Matyáš Fendrych for initiating this project and providing
  constant support; Lukas Fiedler for revising the manuscript; and Huibin Han and
  Arseny Savin for contributing to genotyping. This work was supported by the Austrian
  Science Fund (FWF) I 3630-B25 (to J.F.) and the Doctoral Fellowship Progrmme of
  the Austrian Academy of Sciences (to L.L.) We also acknowledge Taif University Researchers
  Supporting Project TURSP-HC2021/02 and funding “Plants as a tool for sustainable
  global development (no. CZ.02.1.01/0.0/0.0/16_019/0000827).”
article_number: e2121058119
article_processing_charge: No
article_type: original
author:
- first_name: Lanxin
  full_name: Li, Lanxin
  id: 367EF8FA-F248-11E8-B48F-1D18A9856A87
  last_name: Li
  orcid: 0000-0002-5607-272X
- first_name: Huihuang
  full_name: Chen, Huihuang
  id: 83c96512-15b2-11ec-abd3-b7eede36184f
  last_name: Chen
- first_name: Saqer S.
  full_name: Alotaibi, Saqer S.
  last_name: Alotaibi
- first_name: Aleš
  full_name: Pěnčík, Aleš
  last_name: Pěnčík
- first_name: Maciek
  full_name: Adamowski, Maciek
  id: 45F536D2-F248-11E8-B48F-1D18A9856A87
  last_name: Adamowski
  orcid: 0000-0001-6463-5257
- first_name: Ondřej
  full_name: Novák, Ondřej
  last_name: Novák
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Li L, Chen H, Alotaibi SS, et al. RALF1 peptide triggers biphasic root growth
    inhibition upstream of auxin biosynthesis. <i>Proceedings of the National Academy
    of Sciences</i>. 2022;119(31). doi:<a href="https://doi.org/10.1073/pnas.2121058119">10.1073/pnas.2121058119</a>
  apa: Li, L., Chen, H., Alotaibi, S. S., Pěnčík, A., Adamowski, M., Novák, O., &#38;
    Friml, J. (2022). RALF1 peptide triggers biphasic root growth inhibition upstream
    of auxin biosynthesis. <i>Proceedings of the National Academy of Sciences</i>.
    Proceedings of the National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.2121058119">https://doi.org/10.1073/pnas.2121058119</a>
  chicago: Li, Lanxin, Huihuang Chen, Saqer S. Alotaibi, Aleš Pěnčík, Maciek Adamowski,
    Ondřej Novák, and Jiří Friml. “RALF1 Peptide Triggers Biphasic Root Growth Inhibition
    Upstream of Auxin Biosynthesis.” <i>Proceedings of the National Academy of Sciences</i>.
    Proceedings of the National Academy of Sciences, 2022. <a href="https://doi.org/10.1073/pnas.2121058119">https://doi.org/10.1073/pnas.2121058119</a>.
  ieee: L. Li <i>et al.</i>, “RALF1 peptide triggers biphasic root growth inhibition
    upstream of auxin biosynthesis,” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 119, no. 31. Proceedings of the National Academy of Sciences, 2022.
  ista: Li L, Chen H, Alotaibi SS, Pěnčík A, Adamowski M, Novák O, Friml J. 2022.
    RALF1 peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis.
    Proceedings of the National Academy of Sciences. 119(31), e2121058119.
  mla: Li, Lanxin, et al. “RALF1 Peptide Triggers Biphasic Root Growth Inhibition
    Upstream of Auxin Biosynthesis.” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 119, no. 31, e2121058119, Proceedings of the National Academy of Sciences,
    2022, doi:<a href="https://doi.org/10.1073/pnas.2121058119">10.1073/pnas.2121058119</a>.
  short: L. Li, H. Chen, S.S. Alotaibi, A. Pěnčík, M. Adamowski, O. Novák, J. Friml,
    Proceedings of the National Academy of Sciences 119 (2022).
date_created: 2022-08-04T20:06:49Z
date_published: 2022-07-25T00:00:00Z
date_updated: 2024-10-29T10:12:30Z
day: '25'
ddc:
- '580'
department:
- _id: GradSch
- _id: JiFr
doi: 10.1073/pnas.2121058119
external_id:
  isi:
  - '000881496900002'
  pmid:
  - '35878023'
file:
- access_level: open_access
  checksum: ae6f19b0d9efba6687f9e4dc1bab1d6e
  content_type: application/pdf
  creator: dernst
  date_created: 2022-08-08T07:42:09Z
  date_updated: 2022-08-08T07:42:09Z
  file_id: '11747'
  file_name: 2022_PNAS_Li.pdf
  file_size: 2506262
  relation: main_file
  success: 1
file_date_updated: 2022-08-08T07:42:09Z
has_accepted_license: '1'
intvolume: '       119'
isi: 1
issue: '31'
keyword:
- Multidisciplinary
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 26538374-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I03630
  name: Molecular mechanisms of endocytic cargo recognition in plants
- _id: 26B4D67E-B435-11E9-9278-68D0E5697425
  grant_number: '25351'
  name: 'A Case Study of Plant Growth Regulation: Molecular Mechanism of Auxin-mediated
    Rapid Growth Inhibition in Arabidopsis Root'
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: Proceedings of the National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: RALF1 peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 119
year: '2022'
...
---
_id: '13240'
abstract:
- lang: eng
  text: Ustilago maydis is a biotrophic phytopathogenic fungus that causes corn smut
    disease. As a well-established model system, U. maydis is genetically fully accessible
    with large omics datasets available and subject to various biological questions
    ranging from DNA-repair, RNA-transport, and protein secretion to disease biology.
    For many genetic approaches, tight control of transgene regulation is important.
    Here we established an optimised version of the Tetracycline-ON (TetON) system
    for U. maydis. We demonstrate the Tetracycline concentration-dependent expression
    of fluorescent protein transgenes and the system’s suitability for the induced
    expression of the toxic protein BCL2 Associated X-1 (Bax1). The Golden Gate compatible
    vector system contains a native minimal promoter from the mating factor a-1 encoding
    gene, mfa with ten copies of the tet-regulated operator (tetO) and a codon optimised
    Tet-repressor (tetR*) which is translationally fused to the native transcriptional
    corepressor Mql1 (UMAG_05501). The metabolism-independent transcriptional regulator
    system is functional both, in liquid culture as well as on solid media in the
    presence of the inducer and can become a useful tool for toxin-antitoxin studies,
    identification of antifungal proteins, and to study functions of toxic gene products
    in Ustilago maydis.
acknowledgement: "The research leading to these results received funding from the
  European Research Council under the European Union’s Seventh Framework Programme
  ERC-2013-STG (grant agreement: 335691), the Austrian Science Fund (I 3033-B22),
  the Austrian Academy of Sciences, and the Deutsche Forschungsgemeinschaft (DFG,
  German Research Foundation) under Germany's Excellence Strategy EXC-2070-390732324
  (PhenoRob) and DFG grant (DJ 64/5-1).\r\nWe would like to thank the GMI/IMBA/IMP
  core facilities for their excellent technical support. We would like to acknowledge
  Dr. Sinéad A. O’Sullivan from DZNE, University of Bonn for providing anti-GFP antibodies.
  The authors are thankful to the Excellence University of Bonn for providing infrastructure
  and instrumentation facilities at the INRES-Plant Pathology department."
article_number: '1029114'
article_processing_charge: Yes
article_type: original
author:
- first_name: Kishor D.
  full_name: Ingole, Kishor D.
  last_name: Ingole
- first_name: Nithya
  full_name: Nagarajan, Nithya
  last_name: Nagarajan
- first_name: Simon
  full_name: Uhse, Simon
  last_name: Uhse
- first_name: Caterina
  full_name: Giannini, Caterina
  id: e3fdddd5-f6e0-11ea-865d-ca99ee6367f4
  last_name: Giannini
- first_name: Armin
  full_name: Djamei, Armin
  last_name: Djamei
citation:
  ama: Ingole KD, Nagarajan N, Uhse S, Giannini C, Djamei A. Tetracycline-controlled
    (TetON) gene expression system for the smut fungus Ustilago maydis. <i>Frontiers
    in Fungal Biology</i>. 2022;3. doi:<a href="https://doi.org/10.3389/ffunb.2022.1029114">10.3389/ffunb.2022.1029114</a>
  apa: Ingole, K. D., Nagarajan, N., Uhse, S., Giannini, C., &#38; Djamei, A. (2022).
    Tetracycline-controlled (TetON) gene expression system for the smut fungus Ustilago
    maydis. <i>Frontiers in Fungal Biology</i>. Frontiers Media. <a href="https://doi.org/10.3389/ffunb.2022.1029114">https://doi.org/10.3389/ffunb.2022.1029114</a>
  chicago: Ingole, Kishor D., Nithya Nagarajan, Simon Uhse, Caterina Giannini, and
    Armin Djamei. “Tetracycline-Controlled (TetON) Gene Expression System for the
    Smut Fungus Ustilago Maydis.” <i>Frontiers in Fungal Biology</i>. Frontiers Media,
    2022. <a href="https://doi.org/10.3389/ffunb.2022.1029114">https://doi.org/10.3389/ffunb.2022.1029114</a>.
  ieee: K. D. Ingole, N. Nagarajan, S. Uhse, C. Giannini, and A. Djamei, “Tetracycline-controlled
    (TetON) gene expression system for the smut fungus Ustilago maydis,” <i>Frontiers
    in Fungal Biology</i>, vol. 3. Frontiers Media, 2022.
  ista: Ingole KD, Nagarajan N, Uhse S, Giannini C, Djamei A. 2022. Tetracycline-controlled
    (TetON) gene expression system for the smut fungus Ustilago maydis. Frontiers
    in Fungal Biology. 3, 1029114.
  mla: Ingole, Kishor D., et al. “Tetracycline-Controlled (TetON) Gene Expression
    System for the Smut Fungus Ustilago Maydis.” <i>Frontiers in Fungal Biology</i>,
    vol. 3, 1029114, Frontiers Media, 2022, doi:<a href="https://doi.org/10.3389/ffunb.2022.1029114">10.3389/ffunb.2022.1029114</a>.
  short: K.D. Ingole, N. Nagarajan, S. Uhse, C. Giannini, A. Djamei, Frontiers in
    Fungal Biology 3 (2022).
date_created: 2023-07-16T22:01:12Z
date_published: 2022-10-19T00:00:00Z
date_updated: 2024-03-06T14:01:57Z
day: '19'
ddc:
- '579'
department:
- _id: JiFr
doi: 10.3389/ffunb.2022.1029114
file:
- access_level: open_access
  checksum: 2254e0119c0749d6f7237084fefcece6
  content_type: application/pdf
  creator: dernst
  date_created: 2023-07-17T11:46:34Z
  date_updated: 2023-07-17T11:46:34Z
  file_id: '13242'
  file_name: 2023_FrontiersFungalBio_Ingole.pdf
  file_size: 27966699
  relation: main_file
  success: 1
file_date_updated: 2023-07-17T11:46:34Z
has_accepted_license: '1'
intvolume: '         3'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
publication: Frontiers in Fungal Biology
publication_identifier:
  eissn:
  - 2673-6128
publication_status: published
publisher: Frontiers Media
quality_controlled: '1'
scopus_import: '1'
status: public
title: Tetracycline-controlled (TetON) gene expression system for the smut fungus
  Ustilago maydis
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2022'
...
---
_id: '10016'
abstract:
- lang: eng
  text: 'Auxin has always been at the forefront of research in plant physiology and
    development. Since the earliest contemplations by Julius von Sachs and Charles
    Darwin, more than a century-long struggle has been waged to understand its function.
    This largely reflects the failures, successes, and inevitable progress in the
    entire field of plant signaling and development. Here I present 14 stations on
    our long and sometimes mystical journey to understand auxin. These highlights
    were selected to give a flavor of the field and to show the scope and limits of
    our current knowledge. A special focus is put on features that make auxin unique
    among phytohormones, such as its dynamic, directional transport network, which
    integrates external and internal signals, including self-organizing feedback.
    Accented are persistent mysteries and controversies. The unexpected discoveries
    related to rapid auxin responses and growth regulation recently disturbed our
    contentment regarding understanding of the auxin signaling mechanism. These new
    revelations, along with advances in technology, usher us into a new, exciting
    era in auxin research. '
acknowledgement: "The author thanks the whole community of researchers consciously
  or unconsciously working on questions related to auxin, whose hard work and enthusiasm
  contributed to development of this exciting story. Particular thanks go to many\r\nbrilliant
  present and past members of the Friml group and our numerous excellent collaborators,
  without whom my own personal journey would not be possible. The way of the cross
  with its 14 stations is a popular devotion among Roman Catholics and inspires them
  to make a spiritual pilgrimage through contemplation of Christ on his last day.
  Its aspects of gradual progress, struggle, passion, and revelation served as an
  inspiration for the formal depiction of our journey to understanding auxin as described
  in this review. It is in no way intended to reflect the personal beliefs of the
  author and readers. I am grateful to Nick Barton, Eva Benková, Lenka Caisová, Matyáš
  Fendrych, Lukáš Fiedler, Monika Frátriková, Jarmila Frimlová, Michelle Gallei, Jakub
  Hajný, Lukas Hoermayer, Alexandra Mally, Ondrˇej Novák, Jan Petrášek, Aleš Pěnčík,
  Steffen Vanneste, Tongda Xu, and Zhenbiao Yang for their valuable comments. Special
  thanks go to Michelle Gallei for her invaluable assistance with the figures."
article_number: a039859
article_processing_charge: No
article_type: review
author:
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Friml J. Fourteen stations of auxin. <i>Cold Spring Harbor Perspectives in
    Biology</i>. 2022;14(5). doi:<a href="https://doi.org/10.1101/cshperspect.a039859
    ">10.1101/cshperspect.a039859 </a>
  apa: Friml, J. (2022). Fourteen stations of auxin. <i>Cold Spring Harbor Perspectives
    in Biology</i>. Cold Spring Harbor Laboratory. <a href="https://doi.org/10.1101/cshperspect.a039859
    ">https://doi.org/10.1101/cshperspect.a039859 </a>
  chicago: Friml, Jiří. “Fourteen Stations of Auxin.” <i>Cold Spring Harbor Perspectives
    in Biology</i>. Cold Spring Harbor Laboratory, 2022. <a href="https://doi.org/10.1101/cshperspect.a039859
    ">https://doi.org/10.1101/cshperspect.a039859 </a>.
  ieee: J. Friml, “Fourteen stations of auxin,” <i>Cold Spring Harbor Perspectives
    in Biology</i>, vol. 14, no. 5. Cold Spring Harbor Laboratory, 2022.
  ista: Friml J. 2022. Fourteen stations of auxin. Cold Spring Harbor Perspectives
    in Biology. 14(5), a039859.
  mla: Friml, Jiří. “Fourteen Stations of Auxin.” <i>Cold Spring Harbor Perspectives
    in Biology</i>, vol. 14, no. 5, a039859, Cold Spring Harbor Laboratory, 2022,
    doi:<a href="https://doi.org/10.1101/cshperspect.a039859 ">10.1101/cshperspect.a039859
    </a>.
  short: J. Friml, Cold Spring Harbor Perspectives in Biology 14 (2022).
date_created: 2021-09-14T11:36:53Z
date_published: 2022-05-27T00:00:00Z
date_updated: 2023-08-02T06:54:42Z
day: '27'
department:
- _id: JiFr
doi: '10.1101/cshperspect.a039859 '
external_id:
  isi:
  - '000806563000003'
  pmid:
  - '34400554'
intvolume: '        14'
isi: 1
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: 'https://doi.org/10.1101/cshperspect.a039859 '
month: '05'
oa: 1
oa_version: Published Version
pmid: 1
publication: Cold Spring Harbor Perspectives in Biology
publication_identifier:
  issn:
  - 1943-0264
publication_status: published
publisher: Cold Spring Harbor Laboratory
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fourteen stations of auxin
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 14
year: '2022'
...
---
_id: '10411'
abstract:
- lang: eng
  text: The phytohormone auxin is the major growth regulator governing tropic responses
    including gravitropism. Auxin build-up at the lower side of stimulated shoots
    promotes cell expansion, whereas in roots it inhibits growth, leading to upward
    shoot bending and downward root bending, respectively. Yet it remains an enigma
    how the same signal can trigger such opposite cellular responses. In this review,
    we discuss several recent unexpected insights into the mechanisms underlying auxin
    regulation of growth, challenging several existing models. We focus on the divergent
    mechanisms of apoplastic pH regulation in shoots and roots revisiting the classical
    Acid Growth Theory and discuss coordinated involvement of multiple auxin signaling
    pathways. From this emerges a more comprehensive, updated picture how auxin regulates
    growth.
acknowledgement: The authors thank Alexandra Mally for editing the text. This work
  was supported by the Austrian Science Fund (FWF) I 3630-B25 to Jiří Friml and the
  DOC Fellowship of the Austrian Academy of Sciences to Lanxin Li. All figures were
  created with BioRender.com.
article_processing_charge: No
article_type: original
author:
- first_name: Lanxin
  full_name: Li, Lanxin
  id: 367EF8FA-F248-11E8-B48F-1D18A9856A87
  last_name: Li
  orcid: 0000-0002-5607-272X
- first_name: Michelle C
  full_name: Gallei, Michelle C
  id: 35A03822-F248-11E8-B48F-1D18A9856A87
  last_name: Gallei
  orcid: 0000-0003-1286-7368
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: 'Li L, Gallei MC, Friml J. Bending to auxin: Fast acid growth for tropisms.
    <i>Trends in Plant Science</i>. 2022;27(5):440-449. doi:<a href="https://doi.org/10.1016/j.tplants.2021.11.006">10.1016/j.tplants.2021.11.006</a>'
  apa: 'Li, L., Gallei, M. C., &#38; Friml, J. (2022). Bending to auxin: Fast acid
    growth for tropisms. <i>Trends in Plant Science</i>. Cell Press. <a href="https://doi.org/10.1016/j.tplants.2021.11.006">https://doi.org/10.1016/j.tplants.2021.11.006</a>'
  chicago: 'Li, Lanxin, Michelle C Gallei, and Jiří Friml. “Bending to Auxin: Fast
    Acid Growth for Tropisms.” <i>Trends in Plant Science</i>. Cell Press, 2022. <a
    href="https://doi.org/10.1016/j.tplants.2021.11.006">https://doi.org/10.1016/j.tplants.2021.11.006</a>.'
  ieee: 'L. Li, M. C. Gallei, and J. Friml, “Bending to auxin: Fast acid growth for
    tropisms,” <i>Trends in Plant Science</i>, vol. 27, no. 5. Cell Press, pp. 440–449,
    2022.'
  ista: 'Li L, Gallei MC, Friml J. 2022. Bending to auxin: Fast acid growth for tropisms.
    Trends in Plant Science. 27(5), 440–449.'
  mla: 'Li, Lanxin, et al. “Bending to Auxin: Fast Acid Growth for Tropisms.” <i>Trends
    in Plant Science</i>, vol. 27, no. 5, Cell Press, 2022, pp. 440–49, doi:<a href="https://doi.org/10.1016/j.tplants.2021.11.006">10.1016/j.tplants.2021.11.006</a>.'
  short: L. Li, M.C. Gallei, J. Friml, Trends in Plant Science 27 (2022) 440–449.
date_created: 2021-12-05T23:01:43Z
date_published: 2022-05-01T00:00:00Z
date_updated: 2024-10-29T10:12:33Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1016/j.tplants.2021.11.006
external_id:
  isi:
  - '000793707900005'
  pmid:
  - '34848141'
file:
- access_level: open_access
  checksum: 3d94980ee1ff6bec100dd813f6a921a6
  content_type: application/pdf
  creator: amally
  date_created: 2023-11-02T17:00:03Z
  date_updated: 2023-11-02T17:00:03Z
  file_id: '14480'
  file_name: Li Plants 2021_accepted.pdf
  file_size: 805779
  relation: main_file
  success: 1
file_date_updated: 2023-11-02T17:00:03Z
has_accepted_license: '1'
intvolume: '        27'
isi: 1
issue: '5'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Submitted Version
page: 440-449
pmid: 1
project:
- _id: 26538374-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I03630
  name: Molecular mechanisms of endocytic cargo recognition in plants
- _id: 26B4D67E-B435-11E9-9278-68D0E5697425
  grant_number: '25351'
  name: 'A Case Study of Plant Growth Regulation: Molecular Mechanism of Auxin-mediated
    Rapid Growth Inhibition in Arabidopsis Root'
publication: Trends in Plant Science
publication_identifier:
  issn:
  - 1360-1385
publication_status: published
publisher: Cell Press
quality_controlled: '1'
related_material:
  record:
  - id: '11626'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 'Bending to auxin: Fast acid growth for tropisms'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 27
year: '2022'
...
---
_id: '10583'
abstract:
- lang: eng
  text: The synthetic strigolactone (SL) analog, rac-GR24, has been instrumental in
    studying the role of SLs as well as karrikins because it activates the receptors
    DWARF14 (D14) and KARRIKIN INSENSITIVE 2 (KAI2) of their signaling pathways, respectively.
    Treatment with rac-GR24 modifies the root architecture at different levels, such
    as decreasing the lateral root density (LRD), while promoting root hair elongation
    or flavonol accumulation. Previously, we have shown that the flavonol biosynthesis
    is transcriptionally activated in the root by rac-GR24 treatment, but, thus far,
    the molecular players involved in that response have remained unknown. To get
    an in-depth insight into the changes that occur after the compound is perceived
    by the roots, we compared the root transcriptomes of the wild type and the more
    axillary growth2 (max2) mutant, affected in both SL and karrikin signaling pathways,
    with and without rac-GR24 treatment. Quantitative reverse transcription (qRT)-PCR,
    reporter line analysis and mutant phenotyping indicated that the flavonol response
    and the root hair elongation are controlled by the ELONGATED HYPOCOTYL 5 (HY5)
    and MYB12 transcription factors, but HY5, in contrast to MYB12, affects the LRD
    as well. Furthermore, we identified the transcription factors TARGET OF MONOPTEROS
    5 (TMO5) and TMO5 LIKE1 as negative and the Mediator complex as positive regulators
    of the rac-GR24 effect on LRD. Altogether, hereby, we get closer toward understanding
    the molecular mechanisms that underlay the rac-GR24 responses in the root.
acknowledgement: The authors thank Ralf Stracke (Bielefeld University, Bielefeld,
  Germany) for providing the myb mutants and their colleagues Bert De Rybel for the
  tmo5t;mo5l1 double mutant, Boris Parizot for tips on the RNA-seq analysis, Veronique
  Storme for statistical help on both the RNA-seq and lateral root density, and Martine
  De Cock for help in preparing the manuscript.
article_processing_charge: No
article_type: original
author:
- first_name: Sylwia
  full_name: Struk, Sylwia
  last_name: Struk
- first_name: Lukas
  full_name: Braem, Lukas
  last_name: Braem
- first_name: Cedrick
  full_name: Matthys, Cedrick
  last_name: Matthys
- first_name: Alan
  full_name: Walton, Alan
  last_name: Walton
- first_name: Nick
  full_name: Vangheluwe, Nick
  last_name: Vangheluwe
- first_name: Stan
  full_name: Van Praet, Stan
  last_name: Van Praet
- first_name: Lingxiang
  full_name: Jiang, Lingxiang
  last_name: Jiang
- first_name: Pawel
  full_name: Baster, Pawel
  id: 3028BD74-F248-11E8-B48F-1D18A9856A87
  last_name: Baster
- first_name: Carolien
  full_name: De Cuyper, Carolien
  last_name: De Cuyper
- first_name: Francois-Didier
  full_name: Boyer, Francois-Didier
  last_name: Boyer
- first_name: Elisabeth
  full_name: Stes, Elisabeth
  last_name: Stes
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Kris
  full_name: Gevaert, Kris
  last_name: Gevaert
- first_name: Sofie
  full_name: Goormachtig, Sofie
  last_name: Goormachtig
citation:
  ama: Struk S, Braem L, Matthys C, et al. Transcriptional analysis in the Arabidopsis
    roots reveals new regulators that link rac-GR24 treatment with changes in flavonol
    accumulation, root hair elongation and lateral root density. <i>Plant &#38; Cell
    Physiology</i>. 2022;63(1):104-119. doi:<a href="https://doi.org/10.1093/pcp/pcab149">10.1093/pcp/pcab149</a>
  apa: Struk, S., Braem, L., Matthys, C., Walton, A., Vangheluwe, N., Van Praet, S.,
    … Goormachtig, S. (2022). Transcriptional analysis in the Arabidopsis roots reveals
    new regulators that link rac-GR24 treatment with changes in flavonol accumulation,
    root hair elongation and lateral root density. <i>Plant &#38; Cell Physiology</i>.
    Oxford University Press. <a href="https://doi.org/10.1093/pcp/pcab149">https://doi.org/10.1093/pcp/pcab149</a>
  chicago: Struk, Sylwia, Lukas Braem, Cedrick Matthys, Alan Walton, Nick Vangheluwe,
    Stan Van Praet, Lingxiang Jiang, et al. “Transcriptional Analysis in the Arabidopsis
    Roots Reveals New Regulators That Link Rac-GR24 Treatment with Changes in Flavonol
    Accumulation, Root Hair Elongation and Lateral Root Density.” <i>Plant &#38; Cell
    Physiology</i>. Oxford University Press, 2022. <a href="https://doi.org/10.1093/pcp/pcab149">https://doi.org/10.1093/pcp/pcab149</a>.
  ieee: S. Struk <i>et al.</i>, “Transcriptional analysis in the Arabidopsis roots
    reveals new regulators that link rac-GR24 treatment with changes in flavonol accumulation,
    root hair elongation and lateral root density,” <i>Plant &#38; Cell Physiology</i>,
    vol. 63, no. 1. Oxford University Press, pp. 104–119, 2022.
  ista: Struk S, Braem L, Matthys C, Walton A, Vangheluwe N, Van Praet S, Jiang L,
    Baster P, De Cuyper C, Boyer F-D, Stes E, Beeckman T, Friml J, Gevaert K, Goormachtig
    S. 2022. Transcriptional analysis in the Arabidopsis roots reveals new regulators
    that link rac-GR24 treatment with changes in flavonol accumulation, root hair
    elongation and lateral root density. Plant &#38; Cell Physiology. 63(1), 104–119.
  mla: Struk, Sylwia, et al. “Transcriptional Analysis in the Arabidopsis Roots Reveals
    New Regulators That Link Rac-GR24 Treatment with Changes in Flavonol Accumulation,
    Root Hair Elongation and Lateral Root Density.” <i>Plant &#38; Cell Physiology</i>,
    vol. 63, no. 1, Oxford University Press, 2022, pp. 104–19, doi:<a href="https://doi.org/10.1093/pcp/pcab149">10.1093/pcp/pcab149</a>.
  short: S. Struk, L. Braem, C. Matthys, A. Walton, N. Vangheluwe, S. Van Praet, L.
    Jiang, P. Baster, C. De Cuyper, F.-D. Boyer, E. Stes, T. Beeckman, J. Friml, K.
    Gevaert, S. Goormachtig, Plant &#38; Cell Physiology 63 (2022) 104–119.
date_created: 2021-12-28T11:44:18Z
date_published: 2022-01-21T00:00:00Z
date_updated: 2023-08-02T13:40:43Z
day: '21'
department:
- _id: JiFr
doi: 10.1093/pcp/pcab149
external_id:
  isi:
  - '000877899400009'
  pmid:
  - '34791413'
intvolume: '        63'
isi: 1
issue: '1'
keyword:
- flavonols
- MAX2
- rac-Gr24
- RNA-seq
- root development
- transcriptional regulation
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1093/pcp/pcab149
month: '01'
oa: 1
oa_version: Published Version
page: 104-119
pmid: 1
publication: Plant & Cell Physiology
publication_identifier:
  eissn:
  - 1471-9053
  issn:
  - 0032-0781
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Transcriptional analysis in the Arabidopsis roots reveals new regulators that
  link rac-GR24 treatment with changes in flavonol accumulation, root hair elongation
  and lateral root density
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 63
year: '2022'
...
---
_id: '12052'
abstract:
- lang: eng
  text: Directionality in the intercellular transport of the plant hormone auxin is
    determined by polar plasma membrane localization of PIN-FORMED (PIN) auxin transport
    proteins. However, apart from PIN phosphorylation at conserved motifs, no further
    determinants explicitly controlling polar PIN sorting decisions have been identified.
    Here we present Arabidopsis WAVY GROWTH 3 (WAV3) and closely related RING-finger
    E3 ubiquitin ligases, whose loss-of-function mutants show a striking apical-to-basal
    polarity switch in PIN2 localization in root meristem cells. WAV3 E3 ligases function
    as essential determinants for PIN polarity, acting independently from PINOID/WAG-dependent
    PIN phosphorylation. They antagonize ectopic deposition of de novo synthesized
    PIN proteins already immediately following completion of cell division, presumably
    via preventing PIN sorting into basal, ARF GEF-mediated trafficking. Our findings
    reveal an involvement of E3 ligases in the selective targeting of apically localized
    PINs in higher plants.
acknowledgement: We would like to thank Tatsuo Sakai, Marcus Heisler, Toru Fujiwara,
  Lucia Strader, Christian Hardtke, Malcolm Bennett, Claus Schwechheimer, Gerd Jürgens
  and Remko Offringa for sharing published materials and Alba Grau Gimeno for support.
  We are greatly indebted to Bert de Rybel for supporting N.K. and M.G. to work on
  the final stages of manuscript preparation as postdocs in his laboratory. A full-length
  SOR1 cDNA clone (J090099M14) was obtained from the National Agriculture and Food
  Research Organization (NARO, Japan). Support by the Multiscale Imaging Core Facility
  at the BOKU is greatly acknowledged. This work has been supported by grants from
  the Austrian Science Fund (FWF P25931-B16; P31493-B25 to Christian Luschnig; I3630-B25
  to Jiří Friml; P30850-B32 to Barbara Korbei) and from the Swiss National Funds (31003A-165877/1
  to Markus Geisler) and the European Union’s Horizon 2020 research and innovation
  program (Marie Skłodowska-Curie grant agreement No 885979 to Matouš Glanc).
article_number: '5147'
article_processing_charge: No
article_type: original
author:
- first_name: N
  full_name: Konstantinova, N
  last_name: Konstantinova
- first_name: Lukas
  full_name: Hörmayer, Lukas
  id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87
  last_name: Hörmayer
- first_name: Matous
  full_name: Glanc, Matous
  id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2
  last_name: Glanc
  orcid: 0000-0003-0619-7783
- first_name: R
  full_name: Keshkeih, R
  last_name: Keshkeih
- first_name: Shutang
  full_name: Tan, Shutang
  id: 2DE75584-F248-11E8-B48F-1D18A9856A87
  last_name: Tan
  orcid: 0000-0002-0471-8285
- first_name: M
  full_name: Di Donato, M
  last_name: Di Donato
- first_name: K
  full_name: Retzer, K
  last_name: Retzer
- first_name: J
  full_name: Moulinier-Anzola, J
  last_name: Moulinier-Anzola
- first_name: M
  full_name: Schwihla, M
  last_name: Schwihla
- first_name: B
  full_name: Korbei, B
  last_name: Korbei
- first_name: M
  full_name: Geisler, M
  last_name: Geisler
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: C
  full_name: Luschnig, C
  last_name: Luschnig
citation:
  ama: Konstantinova N, Hörmayer L, Glanc M, et al. WAVY GROWTH Arabidopsis E3 ubiquitin
    ligases affect apical PIN sorting decisions. <i>Nature Communications</i>. 2022;13.
    doi:<a href="https://doi.org/10.1038/s41467-022-32888-8">10.1038/s41467-022-32888-8</a>
  apa: Konstantinova, N., Hörmayer, L., Glanc, M., Keshkeih, R., Tan, S., Di Donato,
    M., … Luschnig, C. (2022). WAVY GROWTH Arabidopsis E3 ubiquitin ligases affect
    apical PIN sorting decisions. <i>Nature Communications</i>. Springer Nature. <a
    href="https://doi.org/10.1038/s41467-022-32888-8">https://doi.org/10.1038/s41467-022-32888-8</a>
  chicago: Konstantinova, N, Lukas Hörmayer, Matous Glanc, R Keshkeih, Shutang Tan,
    M Di Donato, K Retzer, et al. “WAVY GROWTH Arabidopsis E3 Ubiquitin Ligases Affect
    Apical PIN Sorting Decisions.” <i>Nature Communications</i>. Springer Nature,
    2022. <a href="https://doi.org/10.1038/s41467-022-32888-8">https://doi.org/10.1038/s41467-022-32888-8</a>.
  ieee: N. Konstantinova <i>et al.</i>, “WAVY GROWTH Arabidopsis E3 ubiquitin ligases
    affect apical PIN sorting decisions,” <i>Nature Communications</i>, vol. 13. Springer
    Nature, 2022.
  ista: Konstantinova N, Hörmayer L, Glanc M, Keshkeih R, Tan S, Di Donato M, Retzer
    K, Moulinier-Anzola J, Schwihla M, Korbei B, Geisler M, Friml J, Luschnig C. 2022.
    WAVY GROWTH Arabidopsis E3 ubiquitin ligases affect apical PIN sorting decisions.
    Nature Communications. 13, 5147.
  mla: Konstantinova, N., et al. “WAVY GROWTH Arabidopsis E3 Ubiquitin Ligases Affect
    Apical PIN Sorting Decisions.” <i>Nature Communications</i>, vol. 13, 5147, Springer
    Nature, 2022, doi:<a href="https://doi.org/10.1038/s41467-022-32888-8">10.1038/s41467-022-32888-8</a>.
  short: N. Konstantinova, L. Hörmayer, M. Glanc, R. Keshkeih, S. Tan, M. Di Donato,
    K. Retzer, J. Moulinier-Anzola, M. Schwihla, B. Korbei, M. Geisler, J. Friml,
    C. Luschnig, Nature Communications 13 (2022).
date_created: 2022-09-07T14:19:26Z
date_published: 2022-09-01T00:00:00Z
date_updated: 2023-08-03T13:40:32Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1038/s41467-022-32888-8
external_id:
  isi:
  - '000848744900004'
  pmid:
  - '36050482'
file:
- access_level: open_access
  checksum: 43336758c89cd6c045839089af070afe
  content_type: application/pdf
  creator: dernst
  date_created: 2022-09-08T07:46:16Z
  date_updated: 2022-09-08T07:46:16Z
  file_id: '12063'
  file_name: 2022_NatureCommunications_Konstantinova.pdf
  file_size: 6678579
  relation: main_file
  success: 1
file_date_updated: 2022-09-08T07:46:16Z
has_accepted_license: '1'
intvolume: '        13'
isi: 1
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 26538374-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I03630
  name: Molecular mechanisms of endocytic cargo recognition in plants
publication: Nature Communications
publication_identifier:
  issn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: https://doi.org/10.1038/s41467-022-33198-9
status: public
title: WAVY GROWTH Arabidopsis E3 ubiquitin ligases affect apical PIN sorting decisions
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 13
year: '2022'
...
---
_id: '12053'
abstract:
- lang: eng
  text: Strigolactones (SLs) are a class of phytohormones that regulate plant shoot
    branching and adventitious root development. However, little is known regarding
    the role of SLs in controlling the behavior of the smallest unit of the organism,
    the single cell. Here, taking advantage of a classic single-cell model offered
    by the cotton (Gossypium hirsutum) fiber cell, we show that SLs, whose biosynthesis
    is fine-tuned by gibberellins (GAs), positively regulate cell elongation and cell
    wall thickness by promoting the biosynthesis of very-long-chain fatty acids (VLCFAs)
    and cellulose, respectively. Furthermore, we identified two layers of transcription
    factors (TFs) involved in the hierarchical regulation of this GA-SL crosstalk.
    The top-layer TF GROWTH-REGULATING FACTOR 4 (GhGRF4) directly activates expression
    of the SL biosynthetic gene DWARF27 (D27) to increase SL accumulation in fiber
    cells and GAs induce GhGRF4 expression. SLs induce the expression of four second-layer
    TF genes (GhNAC100-2, GhBLH51, GhGT2, and GhB9SHZ1), which transmit SL signals
    downstream to two ketoacyl-CoA synthase genes (KCS) and three cellulose synthase
    (CesA) genes by directly activating their transcription. Finally, the KCS and
    CesA enzymes catalyze the biosynthesis of very long chain fatty acids and cellulose,
    respectively, to regulate development of high-grade cotton fibers. In addition
    to providing a theoretical basis for cotton fiber improvement, our results shed
    light on SL signaling in plant development at the single-cell level.
acknowledgement: This work was supported by the National Natural Science Foundation
  of China (32070549), Shaanxi Youth Entrusted Talent Program (20190205), Fundamental
  Research Funds for the Central Universities (GK202002005 and GK202201017), Young
  Elite Scientists Sponsorship Program by China Association for Science and Technology
  (CAST) (2019-2021QNRC001), State Key Laboratory of Cotton Biology Open Fund (CB2020A12
  and CB2021A21) and FWF Stand-alone Project (P29988).
article_processing_charge: No
article_type: original
author:
- first_name: Z
  full_name: Tian, Z
  last_name: Tian
- first_name: Yuzhou
  full_name: Zhang, Yuzhou
  id: 3B6137F2-F248-11E8-B48F-1D18A9856A87
  last_name: Zhang
  orcid: 0000-0003-2627-6956
- first_name: L
  full_name: Zhu, L
  last_name: Zhu
- first_name: B
  full_name: Jiang, B
  last_name: Jiang
- first_name: H
  full_name: Wang, H
  last_name: Wang
- first_name: R
  full_name: Gao, R
  last_name: Gao
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: G
  full_name: Xiao, G
  last_name: Xiao
citation:
  ama: Tian Z, Zhang Y, Zhu L, et al. Strigolactones act downstream of gibberellins
    to regulate fiber cell elongation and cell wall thickness in cotton (Gossypium
    hirsutum). <i>The Plant Cell</i>. 2022;34(12):4816-4839. doi:<a href="https://doi.org/10.1093/plcell/koac270">10.1093/plcell/koac270</a>
  apa: Tian, Z., Zhang, Y., Zhu, L., Jiang, B., Wang, H., Gao, R., … Xiao, G. (2022).
    Strigolactones act downstream of gibberellins to regulate fiber cell elongation
    and cell wall thickness in cotton (Gossypium hirsutum). <i>The Plant Cell</i>.
    Oxford University Press. <a href="https://doi.org/10.1093/plcell/koac270">https://doi.org/10.1093/plcell/koac270</a>
  chicago: Tian, Z, Yuzhou Zhang, L Zhu, B Jiang, H Wang, R Gao, Jiří Friml, and G
    Xiao. “Strigolactones Act Downstream of Gibberellins to Regulate Fiber Cell Elongation
    and Cell Wall Thickness in Cotton (Gossypium Hirsutum).” <i>The Plant Cell</i>.
    Oxford University Press, 2022. <a href="https://doi.org/10.1093/plcell/koac270">https://doi.org/10.1093/plcell/koac270</a>.
  ieee: Z. Tian <i>et al.</i>, “Strigolactones act downstream of gibberellins to regulate
    fiber cell elongation and cell wall thickness in cotton (Gossypium hirsutum),”
    <i>The Plant Cell</i>, vol. 34, no. 12. Oxford University Press, pp. 4816–4839,
    2022.
  ista: Tian Z, Zhang Y, Zhu L, Jiang B, Wang H, Gao R, Friml J, Xiao G. 2022. Strigolactones
    act downstream of gibberellins to regulate fiber cell elongation and cell wall
    thickness in cotton (Gossypium hirsutum). The Plant Cell. 34(12), 4816–4839.
  mla: Tian, Z., et al. “Strigolactones Act Downstream of Gibberellins to Regulate
    Fiber Cell Elongation and Cell Wall Thickness in Cotton (Gossypium Hirsutum).”
    <i>The Plant Cell</i>, vol. 34, no. 12, Oxford University Press, 2022, pp. 4816–39,
    doi:<a href="https://doi.org/10.1093/plcell/koac270">10.1093/plcell/koac270</a>.
  short: Z. Tian, Y. Zhang, L. Zhu, B. Jiang, H. Wang, R. Gao, J. Friml, G. Xiao,
    The Plant Cell 34 (2022) 4816–4839.
date_created: 2022-09-07T14:19:39Z
date_published: 2022-12-01T00:00:00Z
date_updated: 2023-08-03T13:41:06Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1093/plcell/koac270
external_id:
  isi:
  - '000852753000001'
  pmid:
  - '36040191'
file:
- access_level: open_access
  checksum: 1c606d9545f29dfca15235f69ad27b58
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-20T08:29:12Z
  date_updated: 2023-01-20T08:29:12Z
  file_id: '12318'
  file_name: 2022_PlantCell_Tian.pdf
  file_size: 3282540
  relation: main_file
  success: 1
file_date_updated: 2023-01-20T08:29:12Z
has_accepted_license: '1'
intvolume: '        34'
isi: 1
issue: '12'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 4816-4839
pmid: 1
project:
- _id: 262EF96E-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P29988
  name: RNA-directed DNA methylation in plant development
publication: The Plant Cell
publication_identifier:
  eissn:
  - 1532-298X
  issn:
  - 1040-4651
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: https://doi.org/10.1093/plcell/koac342
scopus_import: '1'
status: public
title: Strigolactones act downstream of gibberellins to regulate fiber cell elongation
  and cell wall thickness in cotton (Gossypium hirsutum)
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 34
year: '2022'
...
---
_id: '12054'
abstract:
- lang: eng
  text: 'Polar auxin transport is unique to plants and coordinates their growth and
    development1,2. The PIN-FORMED (PIN) auxin transporters exhibit highly asymmetrical
    localizations at the plasma membrane and drive polar auxin transport3,4; however,
    their structures and transport mechanisms remain largely unknown. Here, we report
    three inward-facing conformation structures of Arabidopsis thaliana PIN1: the
    apo state, bound to the natural auxin indole-3-acetic acid (IAA), and in complex
    with the polar auxin transport inhibitor N-1-naphthylphthalamic acid (NPA). The
    transmembrane domain of PIN1 shares a conserved NhaA fold5. In the substrate-bound
    structure, IAA is coordinated by both hydrophobic stacking and hydrogen bonding.
    NPA competes with IAA for the same site at the intracellular pocket, but with
    a much higher affinity. These findings inform our understanding of the substrate
    recognition and transport mechanisms of PINs and set up a framework for future
    research on directional auxin transport, one of the most crucial processes underlying
    plant development.'
acknowledgement: We thank the Cryo-EM Center of the University of Science and Technology
  of China (USTC) and the Center for Biological Imaging (CBI), Institute of Biophysics,
  Chinese Academy of Science, for the EM facility support; we thank B. Zhu, X. Huang
  and all the other staff members for their technical support on cryo-EM data collection.
  We thank J. Ren for his technical support with the transport assays and M. Seeger
  for providing the sybody libraries. This work was supported by the Strategic Priority
  Research Program of Chinese Academy of Sciences (XDB 37020204 to D.L. and XDB37020103
  to Linfeng Sun), National Natural Science Foundation of China (82151215 and 31870726
  to D.L., 31900885 to X.L., and 31870732 to Linfeng Sun), Natural Science Foundation
  of Anhui Province (2008085MC90 to X.L. and 2008085J15 to Linfeng Sun), the Fundamental
  Research Funds for the Central Universities (WK9100000031 to Linfeng Sun), and the
  USTC Research Funds of the Double First-Class Initiative (YD9100002004 to Linfeng
  Sun). Linfeng Sun is supported by an Outstanding Young Scholar Award from the Qiu
  Shi Science and Technologies Foundation, and a Young Scholar Award from the Cyrus
  Tang Foundation.
article_processing_charge: No
article_type: original
author:
- first_name: Z
  full_name: Yang, Z
  last_name: Yang
- first_name: J
  full_name: Xia, J
  last_name: Xia
- first_name: J
  full_name: Hong, J
  last_name: Hong
- first_name: C
  full_name: Zhang, C
  last_name: Zhang
- first_name: H
  full_name: Wei, H
  last_name: Wei
- first_name: W
  full_name: Ying, W
  last_name: Ying
- first_name: C
  full_name: Sun, C
  last_name: Sun
- first_name: L
  full_name: Sun, L
  last_name: Sun
- first_name: Y
  full_name: Mao, Y
  last_name: Mao
- first_name: Y
  full_name: Gao, Y
  last_name: Gao
- first_name: S
  full_name: Tan, S
  last_name: Tan
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: D
  full_name: Li, D
  last_name: Li
- first_name: X
  full_name: Liu, X
  last_name: Liu
- first_name: L
  full_name: Sun, L
  last_name: Sun
citation:
  ama: Yang Z, Xia J, Hong J, et al. Structural insights into auxin recognition and
    efflux by Arabidopsis PIN1. <i>Nature</i>. 2022;609(7927):611-615. doi:<a href="https://doi.org/10.1038/s41586-022-05143-9">10.1038/s41586-022-05143-9</a>
  apa: Yang, Z., Xia, J., Hong, J., Zhang, C., Wei, H., Ying, W., … Sun, L. (2022).
    Structural insights into auxin recognition and efflux by Arabidopsis PIN1. <i>Nature</i>.
    Springer Nature. <a href="https://doi.org/10.1038/s41586-022-05143-9">https://doi.org/10.1038/s41586-022-05143-9</a>
  chicago: Yang, Z, J Xia, J Hong, C Zhang, H Wei, W Ying, C Sun, et al. “Structural
    Insights into Auxin Recognition and Efflux by Arabidopsis PIN1.” <i>Nature</i>.
    Springer Nature, 2022. <a href="https://doi.org/10.1038/s41586-022-05143-9">https://doi.org/10.1038/s41586-022-05143-9</a>.
  ieee: Z. Yang <i>et al.</i>, “Structural insights into auxin recognition and efflux
    by Arabidopsis PIN1,” <i>Nature</i>, vol. 609, no. 7927. Springer Nature, pp.
    611–615, 2022.
  ista: Yang Z, Xia J, Hong J, Zhang C, Wei H, Ying W, Sun C, Sun L, Mao Y, Gao Y,
    Tan S, Friml J, Li D, Liu X, Sun L. 2022. Structural insights into auxin recognition
    and efflux by Arabidopsis PIN1. Nature. 609(7927), 611–615.
  mla: Yang, Z., et al. “Structural Insights into Auxin Recognition and Efflux by
    Arabidopsis PIN1.” <i>Nature</i>, vol. 609, no. 7927, Springer Nature, 2022, pp.
    611–15, doi:<a href="https://doi.org/10.1038/s41586-022-05143-9">10.1038/s41586-022-05143-9</a>.
  short: Z. Yang, J. Xia, J. Hong, C. Zhang, H. Wei, W. Ying, C. Sun, L. Sun, Y. Mao,
    Y. Gao, S. Tan, J. Friml, D. Li, X. Liu, L. Sun, Nature 609 (2022) 611–615.
date_created: 2022-09-07T14:19:52Z
date_published: 2022-08-02T00:00:00Z
date_updated: 2023-08-03T13:41:44Z
day: '02'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1038/s41586-022-05143-9
external_id:
  isi:
  - '000848082900002'
  pmid:
  - '35917925'
file:
- access_level: open_access
  checksum: 3136a585f8e1c7e73b5e1418b3d01898
  content_type: application/pdf
  creator: dernst
  date_created: 2022-09-08T08:02:54Z
  date_updated: 2022-09-08T08:02:54Z
  file_id: '12064'
  file_name: 2022_Nature_Yang.pdf
  file_size: 32344580
  relation: main_file
  success: 1
file_date_updated: 2022-09-08T08:02:54Z
has_accepted_license: '1'
intvolume: '       609'
isi: 1
issue: '7927'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 611-615
pmid: 1
publication: Nature
publication_identifier:
  eissn:
  - 1476-4687
  issn:
  - 0028-0836
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Structural insights into auxin recognition and efflux by Arabidopsis PIN1
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 609
year: '2022'
...
---
_id: '12120'
abstract:
- lang: eng
  text: Plant root architecture flexibly adapts to changing nitrate (NO3−) availability
    in the soil; however, the underlying molecular mechanism of this adaptive development
    remains under-studied. To explore the regulation of NO3−-mediated root growth,
    we screened for low-nitrate-resistant mutant (lonr) and identified mutants that
    were defective in the NAC transcription factor NAC075 (lonr1) as being less sensitive
    to low NO3− in terms of primary root growth. We show that NAC075 is a mobile transcription
    factor relocating from the root stele tissues to the endodermis based on NO3−
    availability. Under low-NO3− availability, the kinase CBL-interacting protein
    kinase 1 (CIPK1) is activated, and it phosphorylates NAC075, restricting its movement
    from the stele, which leads to the transcriptional regulation of downstream target
    WRKY53, consequently leading to adapted root architecture. Our work thus identifies
    an adaptive mechanism involving translocation of transcription factor based on
    nutrient availability and leading to cell-specific reprogramming of plant root
    growth.
acknowledgement: The authors are grateful to Jörg Kudla, Ying Miao, Yu Zheng, Gang
  Li, and Jun Zheng for providing published materials and to Wenkun Zhou and Caifu
  Jiang for helpful discussions. This work was supported by grants from the National
  Key Research and Development Program of China (2021YFF1000500), the National Natural
  Science Foundation of China (32170265 and 32022007), the Beijing Municipal Natural
  Science Foundation (5192011), and the Chinese Universities Scientific Fund (2022TC153).
article_processing_charge: No
article_type: original
author:
- first_name: Huixin
  full_name: Xiao, Huixin
  last_name: Xiao
- first_name: Yumei
  full_name: Hu, Yumei
  last_name: Hu
- first_name: Yaping
  full_name: Wang, Yaping
  last_name: Wang
- first_name: Jinkui
  full_name: Cheng, Jinkui
  last_name: Cheng
- first_name: Jinyi
  full_name: Wang, Jinyi
  last_name: Wang
- first_name: Guojingwei
  full_name: Chen, Guojingwei
  last_name: Chen
- first_name: Qian
  full_name: Li, Qian
  last_name: Li
- first_name: Shuwei
  full_name: Wang, Shuwei
  last_name: Wang
- first_name: Yalu
  full_name: Wang, Yalu
  last_name: Wang
- first_name: Shao-Shuai
  full_name: Wang, Shao-Shuai
  last_name: Wang
- first_name: Yi
  full_name: Wang, Yi
  last_name: Wang
- first_name: Wei
  full_name: Xuan, Wei
  last_name: Xuan
- first_name: Zhen
  full_name: Li, Zhen
  last_name: Li
- first_name: Yan
  full_name: Guo, Yan
  last_name: Guo
- first_name: Zhizhong
  full_name: Gong, Zhizhong
  last_name: Gong
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Jing
  full_name: Zhang, Jing
  last_name: Zhang
citation:
  ama: Xiao H, Hu Y, Wang Y, et al. Nitrate availability controls translocation of
    the transcription factor NAC075 for cell-type-specific reprogramming of root growth.
    <i>Developmental Cell</i>. 2022;57(23):2638-2651.e6. doi:<a href="https://doi.org/10.1016/j.devcel.2022.11.006">10.1016/j.devcel.2022.11.006</a>
  apa: Xiao, H., Hu, Y., Wang, Y., Cheng, J., Wang, J., Chen, G., … Zhang, J. (2022).
    Nitrate availability controls translocation of the transcription factor NAC075
    for cell-type-specific reprogramming of root growth. <i>Developmental Cell</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.devcel.2022.11.006">https://doi.org/10.1016/j.devcel.2022.11.006</a>
  chicago: Xiao, Huixin, Yumei Hu, Yaping Wang, Jinkui Cheng, Jinyi Wang, Guojingwei
    Chen, Qian Li, et al. “Nitrate Availability Controls Translocation of the Transcription
    Factor NAC075 for Cell-Type-Specific Reprogramming of Root Growth.” <i>Developmental
    Cell</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.devcel.2022.11.006">https://doi.org/10.1016/j.devcel.2022.11.006</a>.
  ieee: H. Xiao <i>et al.</i>, “Nitrate availability controls translocation of the
    transcription factor NAC075 for cell-type-specific reprogramming of root growth,”
    <i>Developmental Cell</i>, vol. 57, no. 23. Elsevier, p. 2638–2651.e6, 2022.
  ista: Xiao H, Hu Y, Wang Y, Cheng J, Wang J, Chen G, Li Q, Wang S, Wang Y, Wang
    S-S, Wang Y, Xuan W, Li Z, Guo Y, Gong Z, Friml J, Zhang J. 2022. Nitrate availability
    controls translocation of the transcription factor NAC075 for cell-type-specific
    reprogramming of root growth. Developmental Cell. 57(23), 2638–2651.e6.
  mla: Xiao, Huixin, et al. “Nitrate Availability Controls Translocation of the Transcription
    Factor NAC075 for Cell-Type-Specific Reprogramming of Root Growth.” <i>Developmental
    Cell</i>, vol. 57, no. 23, Elsevier, 2022, p. 2638–2651.e6, doi:<a href="https://doi.org/10.1016/j.devcel.2022.11.006">10.1016/j.devcel.2022.11.006</a>.
  short: H. Xiao, Y. Hu, Y. Wang, J. Cheng, J. Wang, G. Chen, Q. Li, S. Wang, Y. Wang,
    S.-S. Wang, Y. Wang, W. Xuan, Z. Li, Y. Guo, Z. Gong, J. Friml, J. Zhang, Developmental
    Cell 57 (2022) 2638–2651.e6.
date_created: 2023-01-12T11:57:00Z
date_published: 2022-12-05T00:00:00Z
date_updated: 2023-10-04T08:23:20Z
day: '05'
department:
- _id: JiFr
doi: 10.1016/j.devcel.2022.11.006
external_id:
  isi:
  - '000919603800005'
  pmid:
  - '36473460'
intvolume: '        57'
isi: 1
issue: '23'
keyword:
- Developmental Biology
- Cell Biology
- General Biochemistry
- Genetics and Molecular Biology
- Molecular Biology
language:
- iso: eng
month: '12'
oa_version: None
page: 2638-2651.e6
pmid: 1
publication: Developmental Cell
publication_identifier:
  issn:
  - 1534-5807
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nitrate availability controls translocation of the transcription factor NAC075
  for cell-type-specific reprogramming of root growth
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 57
year: '2022'
...
---
_id: '12121'
abstract:
- lang: eng
  text: Autophagosomes are double-membraned vesicles that traffic harmful or unwanted
    cellular macromolecules to the vacuole for recycling. Although autophagosome biogenesis
    has been extensively studied, autophagosome maturation, i.e., delivery and fusion
    with the vacuole, remains largely unknown in plants. Here, we have identified
    an autophagy adaptor, CFS1, that directly interacts with the autophagosome marker
    ATG8 and localizes on both membranes of the autophagosome. Autophagosomes form
    normally in Arabidopsis thaliana cfs1 mutants, but their delivery to the vacuole
    is disrupted. CFS1’s function is evolutionarily conserved in plants, as it also
    localizes to the autophagosomes and plays a role in autophagic flux in the liverwort
    Marchantia polymorpha. CFS1 regulates autophagic flux by bridging autophagosomes
    with the multivesicular body-localized ESCRT-I component VPS23A, leading to the
    formation of amphisomes. Similar to CFS1-ATG8 interaction, disrupting the CFS1-VPS23A
    interaction blocks autophagic flux and renders plants sensitive to nitrogen starvation.
    Altogether, our results reveal a conserved vacuolar sorting hub that regulates
    autophagic flux in plants.
acknowledgement: "We thank Suayip Ustün, Karin Schumacher, Erika Isono, Gerd Juergens,
  Takashi Ueda, Daniel Hofius, and Liwen Jiang for sharing published materials.\r\nWe
  acknowledge funding from Austrian Academy of Sciences, Austrian Science Fund (FWF,
  P 32355, P 34944), Austrian Science Fund (FWF-SFB F79), Vienna Science and Technology\r\nFund
  (WWTF, LS17-047) to Y. Dagdas; Austrian Academy of Sciences DOC Fellowship to J.
  Zhao, Marie Curie VIP2 Fellowship to J.C. De La Concepcion and M. Clavel; Hong Kong
  Research Grant Council (GRF14121019, 14113921, AoE/M-05/12, C4002-17G) to B.-H.
  Kang. We thank Vienna Biocenter Core Facilities (VBCF) Protein Chemistry, Biooptics,
  Plant Sciences, Molecular Biology, and Protein Technologies. We thank J. Matthew
  Watson\r\nand members of the Dagdas lab for the critical reading and editing of
  the manuscript."
article_number: e202203139
article_processing_charge: No
article_type: original
author:
- first_name: Jierui
  full_name: Zhao, Jierui
  last_name: Zhao
- first_name: Mai Thu
  full_name: Bui, Mai Thu
  last_name: Bui
- first_name: Juncai
  full_name: Ma, Juncai
  last_name: Ma
- first_name: Fabian
  full_name: Künzl, Fabian
  last_name: Künzl
- first_name: Lorenzo
  full_name: Picchianti, Lorenzo
  last_name: Picchianti
- first_name: Juan Carlos
  full_name: De La Concepcion, Juan Carlos
  last_name: De La Concepcion
- first_name: Yixuan
  full_name: Chen, Yixuan
  last_name: Chen
- first_name: Sofia
  full_name: Petsangouraki, Sofia
  last_name: Petsangouraki
- first_name: Azadeh
  full_name: Mohseni, Azadeh
  last_name: Mohseni
- first_name: Marta
  full_name: García-Leon, Marta
  last_name: García-Leon
- first_name: Marta Salas
  full_name: Gomez, Marta Salas
  last_name: Gomez
- first_name: Caterina
  full_name: Giannini, Caterina
  id: e3fdddd5-f6e0-11ea-865d-ca99ee6367f4
  last_name: Giannini
- first_name: Dubois
  full_name: Gwennogan, Dubois
  last_name: Gwennogan
- first_name: Roksolana
  full_name: Kobylinska, Roksolana
  last_name: Kobylinska
- first_name: Marion
  full_name: Clavel, Marion
  last_name: Clavel
- first_name: Swen
  full_name: Schellmann, Swen
  last_name: Schellmann
- first_name: Yvon
  full_name: Jaillais, Yvon
  last_name: Jaillais
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Byung-Ho
  full_name: Kang, Byung-Ho
  last_name: Kang
- first_name: Yasin
  full_name: Dagdas, Yasin
  last_name: Dagdas
citation:
  ama: Zhao J, Bui MT, Ma J, et al. Plant autophagosomes mature into amphisomes prior
    to their delivery to the central vacuole. <i>Journal of Cell Biology</i>. 2022;221(12).
    doi:<a href="https://doi.org/10.1083/jcb.202203139">10.1083/jcb.202203139</a>
  apa: Zhao, J., Bui, M. T., Ma, J., Künzl, F., Picchianti, L., De La Concepcion,
    J. C., … Dagdas, Y. (2022). Plant autophagosomes mature into amphisomes prior
    to their delivery to the central vacuole. <i>Journal of Cell Biology</i>. Rockefeller
    University Press. <a href="https://doi.org/10.1083/jcb.202203139">https://doi.org/10.1083/jcb.202203139</a>
  chicago: Zhao, Jierui, Mai Thu Bui, Juncai Ma, Fabian Künzl, Lorenzo Picchianti,
    Juan Carlos De La Concepcion, Yixuan Chen, et al. “Plant Autophagosomes Mature
    into Amphisomes Prior to Their Delivery to the Central Vacuole.” <i>Journal of
    Cell Biology</i>. Rockefeller University Press, 2022. <a href="https://doi.org/10.1083/jcb.202203139">https://doi.org/10.1083/jcb.202203139</a>.
  ieee: J. Zhao <i>et al.</i>, “Plant autophagosomes mature into amphisomes prior
    to their delivery to the central vacuole,” <i>Journal of Cell Biology</i>, vol.
    221, no. 12. Rockefeller University Press, 2022.
  ista: Zhao J, Bui MT, Ma J, Künzl F, Picchianti L, De La Concepcion JC, Chen Y,
    Petsangouraki S, Mohseni A, García-Leon M, Gomez MS, Giannini C, Gwennogan D,
    Kobylinska R, Clavel M, Schellmann S, Jaillais Y, Friml J, Kang B-H, Dagdas Y.
    2022. Plant autophagosomes mature into amphisomes prior to their delivery to the
    central vacuole. Journal of Cell Biology. 221(12), e202203139.
  mla: Zhao, Jierui, et al. “Plant Autophagosomes Mature into Amphisomes Prior to
    Their Delivery to the Central Vacuole.” <i>Journal of Cell Biology</i>, vol. 221,
    no. 12, e202203139, Rockefeller University Press, 2022, doi:<a href="https://doi.org/10.1083/jcb.202203139">10.1083/jcb.202203139</a>.
  short: J. Zhao, M.T. Bui, J. Ma, F. Künzl, L. Picchianti, J.C. De La Concepcion,
    Y. Chen, S. Petsangouraki, A. Mohseni, M. García-Leon, M.S. Gomez, C. Giannini,
    D. Gwennogan, R. Kobylinska, M. Clavel, S. Schellmann, Y. Jaillais, J. Friml,
    B.-H. Kang, Y. Dagdas, Journal of Cell Biology 221 (2022).
date_created: 2023-01-12T11:57:10Z
date_published: 2022-12-01T00:00:00Z
date_updated: 2023-08-03T14:20:15Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1083/jcb.202203139
external_id:
  isi:
  - '000932958800001'
  pmid:
  - '36260289'
file:
- access_level: open_access
  checksum: 050b5cc4b25e6b94fe3e3cbfe0f5c06b
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-23T10:30:11Z
  date_updated: 2023-01-23T10:30:11Z
  file_id: '12342'
  file_name: 2022_JCB_Zhao.pdf
  file_size: 10365777
  relation: main_file
  success: 1
file_date_updated: 2023-01-23T10:30:11Z
has_accepted_license: '1'
intvolume: '       221'
isi: 1
issue: '12'
keyword:
- Cell Biology
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
publication: Journal of Cell Biology
publication_identifier:
  eissn:
  - 1540-8140
  issn:
  - 0021-9525
publication_status: published
publisher: Rockefeller University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Plant autophagosomes mature into amphisomes prior to their delivery to the
  central vacuole
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 221
year: '2022'
...
---
_id: '12130'
abstract:
- lang: eng
  text: Germline determination is essential for species survival and evolution in
    multicellular organisms. In most flowering plants, formation of the female germline
    is initiated with specification of one megaspore mother cell (MMC) in each ovule;
    however, the molecular mechanism underlying this key event remains unclear. Here
    we report that spatially restricted auxin signaling promotes MMC fate in Arabidopsis.
    Our results show that the microRNA160 (miR160) targeted gene ARF17 (AUXIN RESPONSE
    FACTOR17) is required for promoting MMC specification by genetically interacting
    with the SPL/NZZ (SPOROCYTELESS/NOZZLE) gene. Alterations of auxin signaling cause
    formation of supernumerary MMCs in an ARF17- and SPL/NZZ-dependent manner. Furthermore,
    miR160 and ARF17 are indispensable for attaining a normal auxin maximum at the
    ovule apex via modulating the expression domain of PIN1 (PIN-FORMED1) auxin transporter.
    Our findings elucidate the mechanism by which auxin signaling promotes the acquisition
    of female germline cell fate in plants.
acknowledgement: "We thank A. Cheung,W. Lukowitz, V.Walbot, D.Weijers, and R. Yadegari
  for critically reading the manuscript; E. Xiong and G. Zhang for preparing some
  experiments, T. Schuck, J. Gonnering, and P. Engevold for plant care, the Arabidopsis
  Biological Resource Center (ABRC) for ARF10,ARF16, ARF17, EMS1,MIR160a BAC clones
  and cDNAs, the SALK_090804 seed, T. Nakagawa for pGBW vectors, Y. Zhao for the YUC1
  cDNA, Q. Chen for the pHEE401E vector, R. Yadegari for pAT5G01860::n1GFP, pAT5G45980:n1GFP,
  pAT5G50490::n1GFP, pAT5G56200:n1GFP vectors, and D.Weijers for the pGreenII KAN
  SV40-3×GFP and R2D2 vectors, W. Yang for the splmutant, Y. Qin for the pKNU::KNU-VENUS
  vector and seed, G. Tang for the STTM160/160-48 vector, and L. Colombo for pPIN1::PIN1-GFP
  spl and pin1-5 seeds. This work was supported by the US National Science Foundation
  (NSF)-Israel Binational Science Foundation (BSF) research grant to D.Z. (IOS-1322796)
  and T.A. (2012756). D.Z. also\r\ngratefully acknowledges supports of the Shaw Scientist
  Award from the Greater Milwaukee Foundation, USDA National Institute of Food and
  Agriculture (NIFA, 2022-67013-36294), the UWM Discovery and Innovation Grant, the
  Bradley Catalyst Award from the UWM Research\r\nFoundation, and WiSys and UW System
  Applied Research Funding Programs."
article_number: '6960'
article_processing_charge: No
article_type: original
author:
- first_name: Jian
  full_name: Huang, Jian
  last_name: Huang
- first_name: Lei
  full_name: Zhao, Lei
  last_name: Zhao
- first_name: Shikha
  full_name: Malik, Shikha
  last_name: Malik
- first_name: Benjamin R.
  full_name: Gentile, Benjamin R.
  last_name: Gentile
- first_name: Va
  full_name: Xiong, Va
  last_name: Xiong
- first_name: Tzahi
  full_name: Arazi, Tzahi
  last_name: Arazi
- first_name: Heather A.
  full_name: Owen, Heather A.
  last_name: Owen
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Dazhong
  full_name: Zhao, Dazhong
  last_name: Zhao
citation:
  ama: Huang J, Zhao L, Malik S, et al. Specification of female germline by microRNA
    orchestrated auxin signaling in Arabidopsis. <i>Nature Communications</i>. 2022;13.
    doi:<a href="https://doi.org/10.1038/s41467-022-34723-6">10.1038/s41467-022-34723-6</a>
  apa: Huang, J., Zhao, L., Malik, S., Gentile, B. R., Xiong, V., Arazi, T., … Zhao,
    D. (2022). Specification of female germline by microRNA orchestrated auxin signaling
    in Arabidopsis. <i>Nature Communications</i>. Springer Nature. <a href="https://doi.org/10.1038/s41467-022-34723-6">https://doi.org/10.1038/s41467-022-34723-6</a>
  chicago: Huang, Jian, Lei Zhao, Shikha Malik, Benjamin R. Gentile, Va Xiong, Tzahi
    Arazi, Heather A. Owen, Jiří Friml, and Dazhong Zhao. “Specification of Female
    Germline by MicroRNA Orchestrated Auxin Signaling in Arabidopsis.” <i>Nature Communications</i>.
    Springer Nature, 2022. <a href="https://doi.org/10.1038/s41467-022-34723-6">https://doi.org/10.1038/s41467-022-34723-6</a>.
  ieee: J. Huang <i>et al.</i>, “Specification of female germline by microRNA orchestrated
    auxin signaling in Arabidopsis,” <i>Nature Communications</i>, vol. 13. Springer
    Nature, 2022.
  ista: Huang J, Zhao L, Malik S, Gentile BR, Xiong V, Arazi T, Owen HA, Friml J,
    Zhao D. 2022. Specification of female germline by microRNA orchestrated auxin
    signaling in Arabidopsis. Nature Communications. 13, 6960.
  mla: Huang, Jian, et al. “Specification of Female Germline by MicroRNA Orchestrated
    Auxin Signaling in Arabidopsis.” <i>Nature Communications</i>, vol. 13, 6960,
    Springer Nature, 2022, doi:<a href="https://doi.org/10.1038/s41467-022-34723-6">10.1038/s41467-022-34723-6</a>.
  short: J. Huang, L. Zhao, S. Malik, B.R. Gentile, V. Xiong, T. Arazi, H.A. Owen,
    J. Friml, D. Zhao, Nature Communications 13 (2022).
date_created: 2023-01-12T12:02:41Z
date_published: 2022-11-15T00:00:00Z
date_updated: 2023-08-04T08:52:01Z
day: '15'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1038/s41467-022-34723-6
external_id:
  isi:
  - '000884426700001'
  pmid:
  - '36379956'
file:
- access_level: open_access
  checksum: 233922a7b9507d9d48591e6799e4526e
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-23T11:17:33Z
  date_updated: 2023-01-23T11:17:33Z
  file_id: '12346'
  file_name: 2022_NatureCommunications_Huang.pdf
  file_size: 3375249
  relation: main_file
  success: 1
file_date_updated: 2023-01-23T11:17:33Z
has_accepted_license: '1'
intvolume: '        13'
isi: 1
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
- Multidisciplinary
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
  issn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Specification of female germline by microRNA orchestrated auxin signaling in
  Arabidopsis
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 13
year: '2022'
...
---
_id: '12144'
abstract:
- lang: eng
  text: The phytohormone auxin is the major coordinative signal in plant development1,
    mediating transcriptional reprogramming by a well-established canonical signalling
    pathway. TRANSPORT INHIBITOR RESPONSE 1 (TIR1)/AUXIN-SIGNALING F-BOX (AFB) auxin
    receptors are F-box subunits of ubiquitin ligase complexes. In response to auxin,
    they associate with Aux/IAA transcriptional repressors and target them for degradation
    via ubiquitination2,3. Here we identify adenylate cyclase (AC) activity as an
    additional function of TIR1/AFB receptors across land plants. Auxin, together
    with Aux/IAAs, stimulates cAMP production. Three separate mutations in the AC
    motif of the TIR1 C-terminal region, all of which abolish the AC activity, each
    render TIR1 ineffective in mediating gravitropism and sustained auxin-induced
    root growth inhibition, and also affect auxin-induced transcriptional regulation.
    These results highlight the importance of TIR1/AFB AC activity in canonical auxin
    signalling. They also identify a unique phytohormone receptor cassette combining
    F-box and AC motifs, and the role of cAMP as a second messenger in plants.
acknowledged_ssus:
- _id: LifeSc
- _id: Bio
acknowledgement: This research was supported by the Lab Support Facility (LSF) and
  the Imaging and Optics Facility (IOF) of IST Austria. We thank C. Gehring for suggestions
  and advice; and K. U. Torii and G. Stacey for seeds and plasmids. This project was
  funded by a European Research Council Advanced Grant (ETAP-742985). M.F.K. and R.N.
  acknowledge the support of the EU MSCA-IF project CrysPINs (792329). M.K. was supported
  by the project POWR.03.05.00-00-Z302/17 Universitas Copernicana Thoruniensis in
  Futuro–IDS “Academia Copernicana”. CIDG acknowledges support from UKRI under Future
  Leaders Fellowship grant number MR/T020652/1.
article_processing_charge: No
article_type: original
author:
- first_name: Linlin
  full_name: Qi, Linlin
  id: 44B04502-A9ED-11E9-B6FC-583AE6697425
  last_name: Qi
  orcid: 0000-0001-5187-8401
- first_name: Mateusz
  full_name: Kwiatkowski, Mateusz
  last_name: Kwiatkowski
- first_name: Huihuang
  full_name: Chen, Huihuang
  id: 83c96512-15b2-11ec-abd3-b7eede36184f
  last_name: Chen
- first_name: Lukas
  full_name: Hörmayer, Lukas
  id: 2EEE7A2A-F248-11E8-B48F-1D18A9856A87
  last_name: Hörmayer
  orcid: 0000-0001-8295-2926
- first_name: Scott A
  full_name: Sinclair, Scott A
  id: 2D99FE6A-F248-11E8-B48F-1D18A9856A87
  last_name: Sinclair
  orcid: 0000-0002-4566-0593
- first_name: Minxia
  full_name: Zou, Minxia
  id: 5c243f41-03f3-11ec-841c-96faf48a7ef9
  last_name: Zou
- first_name: Charo I.
  full_name: del Genio, Charo I.
  last_name: del Genio
- first_name: Martin F.
  full_name: Kubeš, Martin F.
  last_name: Kubeš
- first_name: Richard
  full_name: Napier, Richard
  last_name: Napier
- first_name: Krzysztof
  full_name: Jaworski, Krzysztof
  last_name: Jaworski
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Qi L, Kwiatkowski M, Chen H, et al. Adenylate cyclase activity of TIR1/AFB
    auxin receptors in plants. <i>Nature</i>. 2022;611(7934):133-138. doi:<a href="https://doi.org/10.1038/s41586-022-05369-7">10.1038/s41586-022-05369-7</a>
  apa: Qi, L., Kwiatkowski, M., Chen, H., Hörmayer, L., Sinclair, S. A., Zou, M.,
    … Friml, J. (2022). Adenylate cyclase activity of TIR1/AFB auxin receptors in
    plants. <i>Nature</i>. Springer Nature. <a href="https://doi.org/10.1038/s41586-022-05369-7">https://doi.org/10.1038/s41586-022-05369-7</a>
  chicago: Qi, Linlin, Mateusz Kwiatkowski, Huihuang Chen, Lukas Hörmayer, Scott A
    Sinclair, Minxia Zou, Charo I. del Genio, et al. “Adenylate Cyclase Activity of
    TIR1/AFB Auxin Receptors in Plants.” <i>Nature</i>. Springer Nature, 2022. <a
    href="https://doi.org/10.1038/s41586-022-05369-7">https://doi.org/10.1038/s41586-022-05369-7</a>.
  ieee: L. Qi <i>et al.</i>, “Adenylate cyclase activity of TIR1/AFB auxin receptors
    in plants,” <i>Nature</i>, vol. 611, no. 7934. Springer Nature, pp. 133–138, 2022.
  ista: Qi L, Kwiatkowski M, Chen H, Hörmayer L, Sinclair SA, Zou M, del Genio CI,
    Kubeš MF, Napier R, Jaworski K, Friml J. 2022. Adenylate cyclase activity of TIR1/AFB
    auxin receptors in plants. Nature. 611(7934), 133–138.
  mla: Qi, Linlin, et al. “Adenylate Cyclase Activity of TIR1/AFB Auxin Receptors
    in Plants.” <i>Nature</i>, vol. 611, no. 7934, Springer Nature, 2022, pp. 133–38,
    doi:<a href="https://doi.org/10.1038/s41586-022-05369-7">10.1038/s41586-022-05369-7</a>.
  short: L. Qi, M. Kwiatkowski, H. Chen, L. Hörmayer, S.A. Sinclair, M. Zou, C.I.
    del Genio, M.F. Kubeš, R. Napier, K. Jaworski, J. Friml, Nature 611 (2022) 133–138.
date_created: 2023-01-12T12:06:05Z
date_published: 2022-11-03T00:00:00Z
date_updated: 2023-10-03T11:04:53Z
day: '03'
department:
- _id: JiFr
doi: 10.1038/s41586-022-05369-7
ec_funded: 1
external_id:
  isi:
  - '000875061600013'
  pmid:
  - '36289340'
intvolume: '       611'
isi: 1
issue: '7934'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://wrap.warwick.ac.uk/168325/1/WRAP-denylate-cyclase-activity-TIR1-AFB-auxin-receptors-root-growth-22.pdf
month: '11'
oa: 1
oa_version: Submitted Version
page: 133-138
pmid: 1
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '742985'
  name: Tracing Evolution of Auxin Transport and Polarity in Plants
publication: Nature
publication_identifier:
  eissn:
  - 1476-4687
  issn:
  - 0028-0836
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Adenylate cyclase activity of TIR1/AFB auxin receptors in plants
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 611
year: '2022'
...
---
_id: '12239'
abstract:
- lang: eng
  text: Biological systems are the sum of their dynamic three-dimensional (3D) parts.
    Therefore, it is critical to study biological structures in 3D and at high resolution
    to gain insights into their physiological functions. Electron microscopy of metal
    replicas of unroofed cells and isolated organelles has been a key technique to
    visualize intracellular structures at nanometer resolution. However, many of these
    methods require specialized equipment and personnel to complete them. Here, we
    present novel accessible methods to analyze biological structures in unroofed
    cells and biochemically isolated organelles in 3D and at nanometer resolution,
    focusing on Arabidopsis clathrin-coated vesicles (CCVs). While CCVs are essential
    trafficking organelles, their detailed structural information is lacking due to
    their poor preservation when observed via classical electron microscopy protocols
    experiments. First, we establish a method to visualize CCVs in unroofed cells
    using scanning transmission electron microscopy tomography, providing sufficient
    resolution to define the clathrin coat arrangements. Critically, the samples are
    prepared directly on electron microscopy grids, removing the requirement to use
    extremely corrosive acids, thereby enabling the use of this method in any electron
    microscopy lab. Secondly, we demonstrate that this standardized sample preparation
    allows the direct comparison of isolated CCV samples with those visualized in
    cells. Finally, to facilitate the high-throughput and robust screening of metal
    replicated samples, we provide a deep learning analysis method to screen the “pseudo
    3D” morphologies of CCVs imaged with 2D modalities. Collectively, our work establishes
    accessible ways to examine the 3D structure of biological samples and provide
    novel insights into the structure of plant CCVs.
acknowledged_ssus:
- _id: EM-Fac
- _id: LifeSc
- _id: Bio
acknowledgement: A.J. is supported by funding from the Austrian Science Fund I3630B25
  (to J.F.). This research was supported by the Scientific Service Units of Institute
  of Science and Technology Austria (ISTA) through resources provided by the Electron
  Microscopy Facility, Lab Support Facility, and the Imaging and Optics Facility.
  We acknowledge Prof. David Robinson (Heidelberg) and Prof. Jan Traas (Lyon) for
  making us aware of previously published classical on-grid preparation methods. No
  conflict of interest declared.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Alexander J
  full_name: Johnson, Alexander J
  id: 46A62C3A-F248-11E8-B48F-1D18A9856A87
  last_name: Johnson
  orcid: 0000-0002-2739-8843
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Christoph M
  full_name: Sommer, Christoph M
  id: 4DF26D8C-F248-11E8-B48F-1D18A9856A87
  last_name: Sommer
  orcid: 0000-0003-1216-9105
- first_name: Tommaso
  full_name: Costanzo, Tommaso
  id: D93824F4-D9BA-11E9-BB12-F207E6697425
  last_name: Costanzo
  orcid: 0000-0001-9732-3815
- first_name: Dana A.
  full_name: Dahhan, Dana A.
  last_name: Dahhan
- first_name: Sebastian Y.
  full_name: Bednarek, Sebastian Y.
  last_name: Bednarek
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Johnson AJ, Kaufmann W, Sommer CM, et al. Three-dimensional visualization of
    planta clathrin-coated vesicles at ultrastructural resolution. <i>Molecular Plant</i>.
    2022;15(10):1533-1542. doi:<a href="https://doi.org/10.1016/j.molp.2022.09.003">10.1016/j.molp.2022.09.003</a>
  apa: Johnson, A. J., Kaufmann, W., Sommer, C. M., Costanzo, T., Dahhan, D. A., Bednarek,
    S. Y., &#38; Friml, J. (2022). Three-dimensional visualization of planta clathrin-coated
    vesicles at ultrastructural resolution. <i>Molecular Plant</i>. Elsevier. <a href="https://doi.org/10.1016/j.molp.2022.09.003">https://doi.org/10.1016/j.molp.2022.09.003</a>
  chicago: Johnson, Alexander J, Walter Kaufmann, Christoph M Sommer, Tommaso Costanzo,
    Dana A. Dahhan, Sebastian Y. Bednarek, and Jiří Friml. “Three-Dimensional Visualization
    of Planta Clathrin-Coated Vesicles at Ultrastructural Resolution.” <i>Molecular
    Plant</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.molp.2022.09.003">https://doi.org/10.1016/j.molp.2022.09.003</a>.
  ieee: A. J. Johnson <i>et al.</i>, “Three-dimensional visualization of planta clathrin-coated
    vesicles at ultrastructural resolution,” <i>Molecular Plant</i>, vol. 15, no.
    10. Elsevier, pp. 1533–1542, 2022.
  ista: Johnson AJ, Kaufmann W, Sommer CM, Costanzo T, Dahhan DA, Bednarek SY, Friml
    J. 2022. Three-dimensional visualization of planta clathrin-coated vesicles at
    ultrastructural resolution. Molecular Plant. 15(10), 1533–1542.
  mla: Johnson, Alexander J., et al. “Three-Dimensional Visualization of Planta Clathrin-Coated
    Vesicles at Ultrastructural Resolution.” <i>Molecular Plant</i>, vol. 15, no.
    10, Elsevier, 2022, pp. 1533–42, doi:<a href="https://doi.org/10.1016/j.molp.2022.09.003">10.1016/j.molp.2022.09.003</a>.
  short: A.J. Johnson, W. Kaufmann, C.M. Sommer, T. Costanzo, D.A. Dahhan, S.Y. Bednarek,
    J. Friml, Molecular Plant 15 (2022) 1533–1542.
date_created: 2023-01-16T09:51:49Z
date_published: 2022-10-03T00:00:00Z
date_updated: 2023-08-04T09:39:24Z
day: '03'
ddc:
- '580'
department:
- _id: JiFr
- _id: EM-Fac
- _id: Bio
doi: 10.1016/j.molp.2022.09.003
external_id:
  isi:
  - '000882769800009'
  pmid:
  - '36081349'
file:
- access_level: open_access
  checksum: 04d5c12490052d03e4dc4412338a43dd
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-30T07:46:51Z
  date_updated: 2023-01-30T07:46:51Z
  file_id: '12435'
  file_name: 2022_MolecularPlant_Johnson.pdf
  file_size: 2307251
  relation: main_file
  success: 1
file_date_updated: 2023-01-30T07:46:51Z
has_accepted_license: '1'
intvolume: '        15'
isi: 1
issue: '10'
keyword:
- Plant Science
- Molecular Biology
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 1533-1542
pmid: 1
project:
- _id: 26538374-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I03630
  name: Molecular mechanisms of endocytic cargo recognition in plants
publication: Molecular Plant
publication_identifier:
  issn:
  - 1674-2052
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Three-dimensional visualization of planta clathrin-coated vesicles at ultrastructural
  resolution
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 15
year: '2022'
...
---
_id: '12291'
abstract:
- lang: eng
  text: The phytohormone auxin triggers transcriptional reprogramming through a well-characterized
    perception machinery in the nucleus. By contrast, mechanisms that underlie fast
    effects of auxin, such as the regulation of ion fluxes, rapid phosphorylation
    of proteins or auxin feedback on its transport, remain unclear1,2,3. Whether auxin-binding
    protein 1 (ABP1) is an auxin receptor has been a source of debate for decades1,4.
    Here we show that a fraction of Arabidopsis thaliana ABP1 is secreted and binds
    auxin specifically at an acidic pH that is typical of the apoplast. ABP1 and its
    plasma-membrane-localized partner, transmembrane kinase 1 (TMK1), are required
    for the auxin-induced ultrafast global phospho-response and for downstream processes
    that include the activation of H+-ATPase and accelerated cytoplasmic streaming.
    abp1 and tmk mutants cannot establish auxin-transporting channels and show defective
    auxin-induced vasculature formation and regeneration. An ABP1(M2X) variant that
    lacks the capacity to bind auxin is unable to complement these defects in abp1
    mutants. These data indicate that ABP1 is the auxin receptor for TMK1-based cell-surface
    signalling, which mediates the global phospho-response and auxin canalization.
acknowledged_ssus:
- _id: Bio
- _id: EM-Fac
- _id: LifeSc
acknowledgement: We acknowledge K. Kubiasová for excellent technical assistance, J.
  Neuhold, A. Lehner and A. Sedivy for technical assistance with protein production
  and purification at Vienna Biocenter Core Facilities; Creoptix for performing GCI;
  and the Bioimaging, Electron Microscopy and Life Science Facilities at ISTA, the
  Plant Sciences Core Facility of CEITEC Masaryk University, the Core Facility CELLIM
  (MEYS CR, LM2018129 Czech-BioImaging) and J. Sprakel for their assistance. J.F.
  is grateful to R. Napier for many insightful suggestions and support. We thank all
  past and present members of the Friml group for their support and for other contributions
  to this effort to clarify the controversial role of ABP1 over the past seven years.
  The project received funding from the European Research Council (ERC) under the
  European Union’s Horizon 2020 research and innovation program (grant agreement no.
  742985 to J.F. and 833867 to D.W.); the Austrian Science Fund (FWF; P29988 to J.F.);
  the Netherlands Organization for Scientific Research (NWO; VICI grant 865.14.001
  to D.W. and VENI grant VI.Veni.212.003 to A.K.); the Ministry of Education, Science
  and Technological Development of the Republic of Serbia (contract no. 451-03-68/2022-14/200053
  to B.D.Ž.); and the MEXT/JSPS KAKENHI to K.T. (20K06685) and T.K. (20H05687 and
  20H05910).
article_processing_charge: No
article_type: original
author:
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Michelle C
  full_name: Gallei, Michelle C
  id: 35A03822-F248-11E8-B48F-1D18A9856A87
  last_name: Gallei
  orcid: 0000-0003-1286-7368
- first_name: Zuzana
  full_name: Gelová, Zuzana
  id: 0AE74790-0E0B-11E9-ABC7-1ACFE5697425
  last_name: Gelová
  orcid: 0000-0003-4783-1752
- first_name: Alexander J
  full_name: Johnson, Alexander J
  id: 46A62C3A-F248-11E8-B48F-1D18A9856A87
  last_name: Johnson
  orcid: 0000-0002-2739-8843
- first_name: Ewa
  full_name: Mazur, Ewa
  last_name: Mazur
- first_name: Aline
  full_name: Monzer, Aline
  id: 2DB5D88C-D7B3-11E9-B8FD-7907E6697425
  last_name: Monzer
- first_name: Lesia
  full_name: Rodriguez Solovey, Lesia
  id: 3922B506-F248-11E8-B48F-1D18A9856A87
  last_name: Rodriguez Solovey
  orcid: 0000-0002-7244-7237
- first_name: Mark
  full_name: Roosjen, Mark
  last_name: Roosjen
- first_name: Inge
  full_name: Verstraeten, Inge
  id: 362BF7FE-F248-11E8-B48F-1D18A9856A87
  last_name: Verstraeten
  orcid: 0000-0001-7241-2328
- first_name: Branka D.
  full_name: Živanović, Branka D.
  last_name: Živanović
- first_name: Minxia
  full_name: Zou, Minxia
  id: 5c243f41-03f3-11ec-841c-96faf48a7ef9
  last_name: Zou
- first_name: Lukas
  full_name: Fiedler, Lukas
  id: 7c417475-8972-11ed-ae7b-8b674ca26986
  last_name: Fiedler
- first_name: Caterina
  full_name: Giannini, Caterina
  id: e3fdddd5-f6e0-11ea-865d-ca99ee6367f4
  last_name: Giannini
- first_name: Peter
  full_name: Grones, Peter
  last_name: Grones
- first_name: Mónika
  full_name: Hrtyan, Mónika
  id: 45A71A74-F248-11E8-B48F-1D18A9856A87
  last_name: Hrtyan
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Andre
  full_name: Kuhn, Andre
  last_name: Kuhn
- first_name: Madhumitha
  full_name: Narasimhan, Madhumitha
  id: 44BF24D0-F248-11E8-B48F-1D18A9856A87
  last_name: Narasimhan
  orcid: 0000-0002-8600-0671
- first_name: Marek
  full_name: Randuch, Marek
  id: 6ac4636d-15b2-11ec-abd3-fb8df79972ae
  last_name: Randuch
- first_name: Nikola
  full_name: Rýdza, Nikola
  last_name: Rýdza
- first_name: Koji
  full_name: Takahashi, Koji
  last_name: Takahashi
- first_name: Shutang
  full_name: Tan, Shutang
  id: 2DE75584-F248-11E8-B48F-1D18A9856A87
  last_name: Tan
  orcid: 0000-0002-0471-8285
- first_name: Anastasiia
  full_name: Teplova, Anastasiia
  id: e3736151-106c-11ec-b916-c2558e2762c6
  last_name: Teplova
- first_name: Toshinori
  full_name: Kinoshita, Toshinori
  last_name: Kinoshita
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
- first_name: Hana
  full_name: Rakusová, Hana
  last_name: Rakusová
citation:
  ama: Friml J, Gallei MC, Gelová Z, et al. ABP1–TMK auxin perception for global phosphorylation
    and auxin canalization. <i>Nature</i>. 2022;609(7927):575-581. doi:<a href="https://doi.org/10.1038/s41586-022-05187-x">10.1038/s41586-022-05187-x</a>
  apa: Friml, J., Gallei, M. C., Gelová, Z., Johnson, A. J., Mazur, E., Monzer, A.,
    … Rakusová, H. (2022). ABP1–TMK auxin perception for global phosphorylation and
    auxin canalization. <i>Nature</i>. Springer Nature. <a href="https://doi.org/10.1038/s41586-022-05187-x">https://doi.org/10.1038/s41586-022-05187-x</a>
  chicago: Friml, Jiří, Michelle C Gallei, Zuzana Gelová, Alexander J Johnson, Ewa
    Mazur, Aline Monzer, Lesia Rodriguez Solovey, et al. “ABP1–TMK Auxin Perception
    for Global Phosphorylation and Auxin Canalization.” <i>Nature</i>. Springer Nature,
    2022. <a href="https://doi.org/10.1038/s41586-022-05187-x">https://doi.org/10.1038/s41586-022-05187-x</a>.
  ieee: J. Friml <i>et al.</i>, “ABP1–TMK auxin perception for global phosphorylation
    and auxin canalization,” <i>Nature</i>, vol. 609, no. 7927. Springer Nature, pp.
    575–581, 2022.
  ista: Friml J, Gallei MC, Gelová Z, Johnson AJ, Mazur E, Monzer A, Rodriguez Solovey
    L, Roosjen M, Verstraeten I, Živanović BD, Zou M, Fiedler L, Giannini C, Grones
    P, Hrtyan M, Kaufmann W, Kuhn A, Narasimhan M, Randuch M, Rýdza N, Takahashi K,
    Tan S, Teplova A, Kinoshita T, Weijers D, Rakusová H. 2022. ABP1–TMK auxin perception
    for global phosphorylation and auxin canalization. Nature. 609(7927), 575–581.
  mla: Friml, Jiří, et al. “ABP1–TMK Auxin Perception for Global Phosphorylation and
    Auxin Canalization.” <i>Nature</i>, vol. 609, no. 7927, Springer Nature, 2022,
    pp. 575–81, doi:<a href="https://doi.org/10.1038/s41586-022-05187-x">10.1038/s41586-022-05187-x</a>.
  short: J. Friml, M.C. Gallei, Z. Gelová, A.J. Johnson, E. Mazur, A. Monzer, L. Rodriguez
    Solovey, M. Roosjen, I. Verstraeten, B.D. Živanović, M. Zou, L. Fiedler, C. Giannini,
    P. Grones, M. Hrtyan, W. Kaufmann, A. Kuhn, M. Narasimhan, M. Randuch, N. Rýdza,
    K. Takahashi, S. Tan, A. Teplova, T. Kinoshita, D. Weijers, H. Rakusová, Nature
    609 (2022) 575–581.
date_created: 2023-01-16T10:04:48Z
date_published: 2022-09-15T00:00:00Z
date_updated: 2023-11-07T08:16:09Z
day: '15'
ddc:
- '580'
department:
- _id: JiFr
- _id: GradSch
- _id: EvBe
- _id: EM-Fac
doi: 10.1038/s41586-022-05187-x
ec_funded: 1
external_id:
  isi:
  - '000851357500002'
  pmid:
  - '36071161'
file:
- access_level: open_access
  checksum: a6055c606aefb900bf62ae3e7d15f921
  content_type: application/pdf
  creator: amally
  date_created: 2023-11-02T17:12:37Z
  date_updated: 2023-11-02T17:12:37Z
  file_id: '14483'
  file_name: Friml Nature 2022_merged.pdf
  file_size: 79774945
  relation: main_file
  success: 1
file_date_updated: 2023-11-02T17:12:37Z
has_accepted_license: '1'
intvolume: '       609'
isi: 1
issue: '7927'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Submitted Version
page: 575-581
pmid: 1
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '742985'
  name: Tracing Evolution of Auxin Transport and Polarity in Plants
- _id: 262EF96E-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P29988
  name: RNA-directed DNA methylation in plant development
publication: Nature
publication_identifier:
  eissn:
  - 1476-4687
  issn:
  - 0028-0836
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: ABP1–TMK auxin perception for global phosphorylation and auxin canalization
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 609
year: '2022'
...
---
_id: '8582'
abstract:
- lang: eng
  text: "Cell and tissue polarization is fundamental for plant growth and morphogenesis.
    The polar, cellular localization of Arabidopsis PIN‐FORMED (PIN) proteins is crucial
    for their function in directional auxin transport. The clustering of PIN polar
    cargoes within the plasma membrane has been proposed to be important for the maintenance
    of their polar distribution. However, the more detailed features of PIN clusters
    and the cellular requirements of cargo clustering remain unclear.\r\nHere, we
    characterized PIN clusters in detail by means of multiple advanced microscopy
    and quantification methods, such as 3D quantitative imaging or freeze‐fracture
    replica labeling. The size and aggregation types of PIN clusters were determined
    by electron microscopy at the nanometer level at different polar domains and at
    different developmental stages, revealing a strong preference for clustering at
    the polar domains.\r\nPharmacological and genetic studies revealed that PIN clusters
    depend on phosphoinositol pathways, cytoskeletal structures and specific cell‐wall
    components as well as connections between the cell wall and the plasma membrane.\r\nThis
    study identifies the role of different cellular processes and structures in polar
    cargo clustering and provides initial mechanistic insight into the maintenance
    of polarity in plants and other systems."
acknowledged_ssus:
- _id: Bio
acknowledgement: We thank Dr Ingo Heilmann (Martin‐Luther‐University Halle‐Wittenberg)
  for the XVE>>PIP5K1‐YFP line, Dr Brad Day (Michigan State University) for the ndr1‐1
  mutant and the complementation lines, and Dr Patricia C. Zambryski (University of
  California, Berkeley) for the 35S::P30‐GFP line, the Bioimaging team (IST Austria)
  for assistance with imaging, group members for discussions, Martine De Cock for
  help in preparing the manuscript and Nataliia Gnyliukh for critical reading and
  revision of the manuscript. This project received funding from the European Research
  Council (ERC) under the European Union's Horizon 2020 research and innovation program
  (grant agreement No. 742985) and Comisión Nacional de Investigación Científica y
  Tecnológica (Project CONICYT‐PAI 82130047). DvW received funding from the People
  Programme (Marie Curie Actions) of the European Union’s Seventh Framework Programme
  (FP7/2007‐2013) under REA grant agreement no. 291734.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Hongjiang
  full_name: Li, Hongjiang
  id: 33CA54A6-F248-11E8-B48F-1D18A9856A87
  last_name: Li
  orcid: 0000-0001-5039-9660
- first_name: Daniel
  full_name: von Wangenheim, Daniel
  id: 49E91952-F248-11E8-B48F-1D18A9856A87
  last_name: von Wangenheim
  orcid: 0000-0002-6862-1247
- first_name: Xixi
  full_name: Zhang, Xixi
  id: 61A66458-47E9-11EA-85BA-8AEAAF14E49A
  last_name: Zhang
  orcid: 0000-0001-7048-4627
- first_name: Shutang
  full_name: Tan, Shutang
  id: 2DE75584-F248-11E8-B48F-1D18A9856A87
  last_name: Tan
  orcid: 0000-0002-0471-8285
- first_name: Nasser
  full_name: Darwish-Miranda, Nasser
  id: 39CD9926-F248-11E8-B48F-1D18A9856A87
  last_name: Darwish-Miranda
  orcid: 0000-0002-8821-8236
- first_name: Satoshi
  full_name: Naramoto, Satoshi
  last_name: Naramoto
- first_name: Krzysztof T
  full_name: Wabnik, Krzysztof T
  id: 4DE369A4-F248-11E8-B48F-1D18A9856A87
  last_name: Wabnik
  orcid: 0000-0001-7263-0560
- first_name: Riet
  full_name: de Rycke, Riet
  last_name: de Rycke
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Daniel J
  full_name: Gütl, Daniel J
  id: 381929CE-F248-11E8-B48F-1D18A9856A87
  last_name: Gütl
- first_name: Ricardo
  full_name: Tejos, Ricardo
  last_name: Tejos
- first_name: Peter
  full_name: Grones, Peter
  id: 399876EC-F248-11E8-B48F-1D18A9856A87
  last_name: Grones
- first_name: Meiyu
  full_name: Ke, Meiyu
  last_name: Ke
- first_name: Xu
  full_name: Chen, Xu
  id: 4E5ADCAA-F248-11E8-B48F-1D18A9856A87
  last_name: Chen
- first_name: Jan
  full_name: Dettmer, Jan
  last_name: Dettmer
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Li H, von Wangenheim D, Zhang X, et al. Cellular requirements for PIN polar
    cargo clustering in Arabidopsis thaliana. <i>New Phytologist</i>. 2021;229(1):351-369.
    doi:<a href="https://doi.org/10.1111/nph.16887">10.1111/nph.16887</a>
  apa: Li, H., von Wangenheim, D., Zhang, X., Tan, S., Darwish-Miranda, N., Naramoto,
    S., … Friml, J. (2021). Cellular requirements for PIN polar cargo clustering in
    Arabidopsis thaliana. <i>New Phytologist</i>. Wiley. <a href="https://doi.org/10.1111/nph.16887">https://doi.org/10.1111/nph.16887</a>
  chicago: Li, Hongjiang, Daniel von Wangenheim, Xixi Zhang, Shutang Tan, Nasser Darwish-Miranda,
    Satoshi Naramoto, Krzysztof T Wabnik, et al. “Cellular Requirements for PIN Polar
    Cargo Clustering in Arabidopsis Thaliana.” <i>New Phytologist</i>. Wiley, 2021.
    <a href="https://doi.org/10.1111/nph.16887">https://doi.org/10.1111/nph.16887</a>.
  ieee: H. Li <i>et al.</i>, “Cellular requirements for PIN polar cargo clustering
    in Arabidopsis thaliana,” <i>New Phytologist</i>, vol. 229, no. 1. Wiley, pp.
    351–369, 2021.
  ista: Li H, von Wangenheim D, Zhang X, Tan S, Darwish-Miranda N, Naramoto S, Wabnik
    KT, de Rycke R, Kaufmann W, Gütl DJ, Tejos R, Grones P, Ke M, Chen X, Dettmer
    J, Friml J. 2021. Cellular requirements for PIN polar cargo clustering in Arabidopsis
    thaliana. New Phytologist. 229(1), 351–369.
  mla: Li, Hongjiang, et al. “Cellular Requirements for PIN Polar Cargo Clustering
    in Arabidopsis Thaliana.” <i>New Phytologist</i>, vol. 229, no. 1, Wiley, 2021,
    pp. 351–69, doi:<a href="https://doi.org/10.1111/nph.16887">10.1111/nph.16887</a>.
  short: H. Li, D. von Wangenheim, X. Zhang, S. Tan, N. Darwish-Miranda, S. Naramoto,
    K.T. Wabnik, R. de Rycke, W. Kaufmann, D.J. Gütl, R. Tejos, P. Grones, M. Ke,
    X. Chen, J. Dettmer, J. Friml, New Phytologist 229 (2021) 351–369.
date_created: 2020-09-28T08:59:28Z
date_published: 2021-01-01T00:00:00Z
date_updated: 2023-08-04T11:01:21Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
- _id: EM-Fac
- _id: Bio
- _id: EvBe
doi: 10.1111/nph.16887
ec_funded: 1
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title: Cellular requirements for PIN polar cargo clustering in Arabidopsis thaliana
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