---
_id: '3084'
abstract:
- lang: eng
  text: |2-

    A central question in developmental biology concerns the mechanism of generation and maintenance of cell polarity, because these processes are essential for many cellular functions and multicellular development [1]. In plants, cell polarity has an additional role in mediating directional transport of the plant hormone auxin that is crucial for multiple developmental processes [2-4]. In addition, plant cells have a complex extracellular matrix, the cell wall [5, 6], whose role in regulating cellular processes, including cell polarity, is unexplored. We have found that polar distribution of PIN auxin transporters [7] in plant cells is maintained by connections between polar domains at the plasma membrane and the cell wall. Genetic and pharmacological interference with cellulose, the major component of the cell wall, or mechanical interference with the cell wall disrupts these connections and leads to increased lateral diffusion and loss of polar distribution of PIN transporters for the phytohormone auxin. Our results reveal a plant-specific mechanism for cell polarity maintenance and provide a conceptual framework for modulating cell polarity and plant development via endogenous and environmental manipulations of the cellulose-based extracellular matrix.
author:
- first_name: Elena
  full_name: Feraru, Elena
  last_name: Feraru
- first_name: Mugurel
  full_name: Feraru, Mugurel I
  last_name: Feraru
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Alexandre
  full_name: Martinière, Alexandre
  last_name: Martinière
- first_name: Grégory
  full_name: Mouille, Grégory
  last_name: Mouille
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Samantha
  full_name: Vernhettes, Samantha
  last_name: Vernhettes
- first_name: John
  full_name: Runions, John
  last_name: Runions
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Feraru E, Feraru M, Kleine Vehn J, et al. PIN polarity maintenance by the cell
    wall in Arabidopsis. <i>Current Biology</i>. 2011;21(4):338-343. doi:<a href="https://doi.org/10.1016/j.cub.2011.01.036">10.1016/j.cub.2011.01.036</a>
  apa: Feraru, E., Feraru, M., Kleine Vehn, J., Martinière, A., Mouille, G., Vanneste,
    S., … Friml, J. (2011). PIN polarity maintenance by the cell wall in Arabidopsis.
    <i>Current Biology</i>. Cell Press. <a href="https://doi.org/10.1016/j.cub.2011.01.036">https://doi.org/10.1016/j.cub.2011.01.036</a>
  chicago: Feraru, Elena, Mugurel Feraru, Jürgen Kleine Vehn, Alexandre Martinière,
    Grégory Mouille, Steffen Vanneste, Samantha Vernhettes, John Runions, and Jiří
    Friml. “PIN Polarity Maintenance by the Cell Wall in Arabidopsis.” <i>Current
    Biology</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.cub.2011.01.036">https://doi.org/10.1016/j.cub.2011.01.036</a>.
  ieee: E. Feraru <i>et al.</i>, “PIN polarity maintenance by the cell wall in Arabidopsis,”
    <i>Current Biology</i>, vol. 21, no. 4. Cell Press, pp. 338–343, 2011.
  ista: Feraru E, Feraru M, Kleine Vehn J, Martinière A, Mouille G, Vanneste S, Vernhettes
    S, Runions J, Friml J. 2011. PIN polarity maintenance by the cell wall in Arabidopsis.
    Current Biology. 21(4), 338–343.
  mla: Feraru, Elena, et al. “PIN Polarity Maintenance by the Cell Wall in Arabidopsis.”
    <i>Current Biology</i>, vol. 21, no. 4, Cell Press, 2011, pp. 338–43, doi:<a href="https://doi.org/10.1016/j.cub.2011.01.036">10.1016/j.cub.2011.01.036</a>.
  short: E. Feraru, M. Feraru, J. Kleine Vehn, A. Martinière, G. Mouille, S. Vanneste,
    S. Vernhettes, J. Runions, J. Friml, Current Biology 21 (2011) 338–343.
date_created: 2018-12-11T12:01:17Z
date_published: 2011-02-22T00:00:00Z
date_updated: 2021-01-12T07:40:56Z
day: '22'
doi: 10.1016/j.cub.2011.01.036
extern: 1
intvolume: '        21'
issue: '4'
month: '02'
page: 338 - 343
publication: Current Biology
publication_status: published
publisher: Cell Press
publist_id: '3618'
quality_controlled: 0
status: public
title: PIN polarity maintenance by the cell wall in Arabidopsis
type: journal_article
volume: 21
year: '2011'
...
---
_id: '3085'
abstract:
- lang: eng
  text: Phototropism is an adaptation response, through which plants grow towards
    the light. It involves light perception and asymmetric distribution of the plant
    hormone auxin. Here we identify a crucial part of the mechanism for phototropism,
    revealing how light perception initiates auxin redistribution that leads to directional
    growth. We show that light polarizes the cellular localization of the auxin efflux
    carrier PIN3 in hypocotyl endodermis cells, resulting in changes in auxin distribution
    and differential growth. In the dark, high expression and activity of the PINOID
    (PID) kinase correlates with apolar targeting of PIN3 to all cell sides. Following
    illumination, light represses PINOID transcription and PIN3 is polarized specifically
    to the inner cell sides by GNOM ARF GTPase GEF (guanine nucleotide exchange factor)-dependent
    trafficking. Thus, differential trafficking at the shaded and illuminated hypocotyl
    side aligns PIN3 polarity with the light direction, and presumably redirects auxin
    flow towards the shaded side, where auxin promotes growth, causing hypocotyls
    to bend towards the light. Our results imply that PID phosphorylation-dependent
    recruitment of PIN proteins into distinct trafficking pathways is a mechanism
    to polarize auxin fluxes in response to different environmental and endogenous
    cues.
author:
- first_name: Zhaojun
  full_name: Ding, Zhaojun
  last_name: Ding
- first_name: Carlos
  full_name: Galván-Ampudia, Carlos S
  last_name: Galván Ampudia
- first_name: Emilie
  full_name: Demarsy, Emilie
  last_name: Demarsy
- first_name: Łukasz
  full_name: Łangowski, Łukasz
  last_name: Łangowski
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Yuanwei
  full_name: Fan, Yuanwei
  last_name: Fan
- first_name: Miyo
  full_name: Morita, Miyo T
  last_name: Morita
- first_name: Masao
  full_name: Tasaka, Masao
  last_name: Tasaka
- first_name: Christian
  full_name: Fankhauser, Christian
  last_name: Fankhauser
- first_name: Remko
  full_name: Offringa, Remko
  last_name: Offringa
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Ding Z, Galván Ampudia C, Demarsy E, et al. Light-mediated polarization of
    the PIN3 auxin transporter for the phototropic response in Arabidopsis. <i>Nature
    Cell Biology</i>. 2011;13(4):447-453. doi:<a href="https://doi.org/10.1038/ncb2208">10.1038/ncb2208</a>
  apa: Ding, Z., Galván Ampudia, C., Demarsy, E., Łangowski, Ł., Kleine Vehn, J.,
    Fan, Y., … Friml, J. (2011). Light-mediated polarization of the PIN3 auxin transporter
    for the phototropic response in Arabidopsis. <i>Nature Cell Biology</i>. Nature
    Publishing Group. <a href="https://doi.org/10.1038/ncb2208">https://doi.org/10.1038/ncb2208</a>
  chicago: Ding, Zhaojun, Carlos Galván Ampudia, Emilie Demarsy, Łukasz Łangowski,
    Jürgen Kleine Vehn, Yuanwei Fan, Miyo Morita, et al. “Light-Mediated Polarization
    of the PIN3 Auxin Transporter for the Phototropic Response in Arabidopsis.” <i>Nature
    Cell Biology</i>. Nature Publishing Group, 2011. <a href="https://doi.org/10.1038/ncb2208">https://doi.org/10.1038/ncb2208</a>.
  ieee: Z. Ding <i>et al.</i>, “Light-mediated polarization of the PIN3 auxin transporter
    for the phototropic response in Arabidopsis,” <i>Nature Cell Biology</i>, vol.
    13, no. 4. Nature Publishing Group, pp. 447–453, 2011.
  ista: Ding Z, Galván Ampudia C, Demarsy E, Łangowski Ł, Kleine Vehn J, Fan Y, Morita
    M, Tasaka M, Fankhauser C, Offringa R, Friml J. 2011. Light-mediated polarization
    of the PIN3 auxin transporter for the phototropic response in Arabidopsis. Nature
    Cell Biology. 13(4), 447–453.
  mla: Ding, Zhaojun, et al. “Light-Mediated Polarization of the PIN3 Auxin Transporter
    for the Phototropic Response in Arabidopsis.” <i>Nature Cell Biology</i>, vol.
    13, no. 4, Nature Publishing Group, 2011, pp. 447–53, doi:<a href="https://doi.org/10.1038/ncb2208">10.1038/ncb2208</a>.
  short: Z. Ding, C. Galván Ampudia, E. Demarsy, Ł. Łangowski, J. Kleine Vehn, Y.
    Fan, M. Morita, M. Tasaka, C. Fankhauser, R. Offringa, J. Friml, Nature Cell Biology
    13 (2011) 447–453.
date_created: 2018-12-11T12:01:17Z
date_published: 2011-04-01T00:00:00Z
date_updated: 2021-01-12T07:40:57Z
day: '01'
doi: 10.1038/ncb2208
extern: 1
intvolume: '        13'
issue: '4'
month: '04'
page: 447 - 453
publication: Nature Cell Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '3616'
quality_controlled: 0
status: public
title: Light-mediated polarization of the PIN3 auxin transporter for the phototropic
  response in Arabidopsis
type: journal_article
volume: 13
year: '2011'
...
---
_id: '3086'
abstract:
- lang: eng
  text: PIN-FORMED (PIN)-dependent auxin transport is essential for plant development
    and its modulation in response to the environment or endogenous signals. A NON-PHOTOTROPIC
    HYPOCOTYL 3 (NPH3)-like protein, MACCHI-BOU 4 (MAB4), has been shown to control
    PIN1 localization during organ formation, but its contribution is limited. The
    Arabidopsis genome contains four genes, MAB4/ENP/NPY1-LIKE1 (MEL1), MEL2, MEL3
    and MEL4, highly homologous to MAB4. Genetic analysis disclosed functional redundancy
    between MAB4 and MEL genes in regulation of not only organ formation but also
    of root gravitropism, revealing that NPH3 family proteins have a wider range of
    functions than previously suspected. Multiple mutants showed severe reduction
    in PIN abundance and PIN polar localization, leading to defective expression of
    an auxin responsive marker DR5rev::GFP. Pharmacological analyses and fluorescence
    recovery after photo-bleaching experiments showed that mel mutations increase
    PIN2 internalization from the plasma membrane, but affect neither intracellular
    PIN2 trafficking nor PIN2 lateral diffusion at the plasma membrane. Notably, all
    MAB4 subfamily proteins show polar localization at the cell periphery in plants.
    The MAB4 polarity was almost identical to PIN polarity. Our results suggest that
    the MAB4 subfamily proteins specifically retain PIN proteins in a polarized manner
    at the plasma membrane, thus controlling directional auxin transport and plant
    development.
author:
- first_name: Masahiko
  full_name: Furutani, Masahiko
  last_name: Furutani
- first_name: Norihito
  full_name: Sakamoto, Norihito
  last_name: Sakamoto
- first_name: Shuhei
  full_name: Yoshida, Shuhei
  last_name: Yoshida
- first_name: Takahito
  full_name: Kajiwara, Takahito
  last_name: Kajiwara
- first_name: Hélène
  full_name: Robert, Hélène S
  last_name: Robert
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Masao
  full_name: Tasaka, Masao
  last_name: Tasaka
citation:
  ama: Furutani M, Sakamoto N, Yoshida S, et al. Polar localized NPH3-like proteins
    regulate polarity and endocytosis of PIN-FORMED auxin efflux carriers. <i>Development</i>.
    2011;138(10):2069-2078. doi:<a href="https://doi.org/10.1242/dev.057745">10.1242/dev.057745</a>
  apa: Furutani, M., Sakamoto, N., Yoshida, S., Kajiwara, T., Robert, H., Friml, J.,
    &#38; Tasaka, M. (2011). Polar localized NPH3-like proteins regulate polarity
    and endocytosis of PIN-FORMED auxin efflux carriers. <i>Development</i>. Company
    of Biologists. <a href="https://doi.org/10.1242/dev.057745">https://doi.org/10.1242/dev.057745</a>
  chicago: Furutani, Masahiko, Norihito Sakamoto, Shuhei Yoshida, Takahito Kajiwara,
    Hélène Robert, Jiří Friml, and Masao Tasaka. “Polar Localized NPH3-like Proteins
    Regulate Polarity and Endocytosis of PIN-FORMED Auxin Efflux Carriers.” <i>Development</i>.
    Company of Biologists, 2011. <a href="https://doi.org/10.1242/dev.057745">https://doi.org/10.1242/dev.057745</a>.
  ieee: M. Furutani <i>et al.</i>, “Polar localized NPH3-like proteins regulate polarity
    and endocytosis of PIN-FORMED auxin efflux carriers,” <i>Development</i>, vol.
    138, no. 10. Company of Biologists, pp. 2069–2078, 2011.
  ista: Furutani M, Sakamoto N, Yoshida S, Kajiwara T, Robert H, Friml J, Tasaka M.
    2011. Polar localized NPH3-like proteins regulate polarity and endocytosis of
    PIN-FORMED auxin efflux carriers. Development. 138(10), 2069–2078.
  mla: Furutani, Masahiko, et al. “Polar Localized NPH3-like Proteins Regulate Polarity
    and Endocytosis of PIN-FORMED Auxin Efflux Carriers.” <i>Development</i>, vol.
    138, no. 10, Company of Biologists, 2011, pp. 2069–78, doi:<a href="https://doi.org/10.1242/dev.057745">10.1242/dev.057745</a>.
  short: M. Furutani, N. Sakamoto, S. Yoshida, T. Kajiwara, H. Robert, J. Friml, M.
    Tasaka, Development 138 (2011) 2069–2078.
date_created: 2018-12-11T12:01:17Z
date_published: 2011-05-01T00:00:00Z
date_updated: 2021-01-12T07:40:57Z
day: '01'
doi: 10.1242/dev.057745
extern: 1
intvolume: '       138'
issue: '10'
month: '05'
page: 2069 - 2078
publication: Development
publication_status: published
publisher: Company of Biologists
publist_id: '3615'
quality_controlled: 0
status: public
title: Polar localized NPH3-like proteins regulate polarity and endocytosis of PIN-FORMED
  auxin efflux carriers
type: journal_article
volume: 138
year: '2011'
...
---
_id: '3087'
abstract:
- lang: eng
  text: Endocytosis is a crucial mechanism by which eukaryotic cells internalize extracellular
    and plasma membrane material, and it is required for a multitude of cellular and
    developmental processes in unicellular and multicellular organisms. In animals
    and yeast, the best characterized pathway for endocytosis depends on the function
    of the vesicle coat protein clathrin. Clathrinmediated endocytosis has recently
    been demonstrated also in plant cells, but its physiological and developmental
    roles remain unclear. Here, we assessed the roles of the clathrin-mediated mechanism
    of endocytosis in plants by genetic means. We interfered with clathrin heavy chain
    (CHC) function through mutants and dominant-negative approaches in Arabidopsis
    thaliana and established tools to manipulate clathrin function in a cell type-specific
    manner. The chc2 single mutants and dominant-negative CHC1 (HUB) transgenic lines
    were defective in bulk endocytosis as well as in internalization of prominent
    plasma membrane proteins. Interference with clathrin-mediated endocytosis led
    to defects in constitutive endocytic recycling of PIN auxin transporters and their
    polar distribution in embryos and roots. Consistent with this, these lines had
    altered auxin distribution patterns and associated auxin transport-related phenotypes,
    such as aberrant embryo patterning, imperfect cotyledon specification, agravitropic
    growth, and impaired lateral root organogenesis. Together, these data demonstrate
    a fundamental role for clathrin function in cell polarity, growth, patterning,
    and organogenesis in plants.
author:
- first_name: Saeko
  full_name: Kitakura, Saeko
  last_name: Kitakura
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
- first_name: Christian
  full_name: Löfke, Christian
  last_name: Löfke
- first_name: Thomas
  full_name: Teichmann, Thomas
  last_name: Teichmann
- first_name: Hirokazu
  full_name: Tanaka, Hirokazu
  last_name: Tanaka
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Kitakura S, Vanneste S, Robert S, et al. Clathrin mediates endocytosis and
    polar distribution of PIN auxin transporters in Arabidopsis. <i>Plant Cell</i>.
    2011;23(5):1920-1931. doi:<a href="https://doi.org/10.1105/tpc.111.083030">10.1105/tpc.111.083030</a>
  apa: Kitakura, S., Vanneste, S., Robert, S., Löfke, C., Teichmann, T., Tanaka, H.,
    &#38; Friml, J. (2011). Clathrin mediates endocytosis and polar distribution of
    PIN auxin transporters in Arabidopsis. <i>Plant Cell</i>. American Society of
    Plant Biologists. <a href="https://doi.org/10.1105/tpc.111.083030">https://doi.org/10.1105/tpc.111.083030</a>
  chicago: Kitakura, Saeko, Steffen Vanneste, Stéphanie Robert, Christian Löfke, Thomas
    Teichmann, Hirokazu Tanaka, and Jiří Friml. “Clathrin Mediates Endocytosis and
    Polar Distribution of PIN Auxin Transporters in Arabidopsis.” <i>Plant Cell</i>.
    American Society of Plant Biologists, 2011. <a href="https://doi.org/10.1105/tpc.111.083030">https://doi.org/10.1105/tpc.111.083030</a>.
  ieee: S. Kitakura <i>et al.</i>, “Clathrin mediates endocytosis and polar distribution
    of PIN auxin transporters in Arabidopsis,” <i>Plant Cell</i>, vol. 23, no. 5.
    American Society of Plant Biologists, pp. 1920–1931, 2011.
  ista: Kitakura S, Vanneste S, Robert S, Löfke C, Teichmann T, Tanaka H, Friml J.
    2011. Clathrin mediates endocytosis and polar distribution of PIN auxin transporters
    in Arabidopsis. Plant Cell. 23(5), 1920–1931.
  mla: Kitakura, Saeko, et al. “Clathrin Mediates Endocytosis and Polar Distribution
    of PIN Auxin Transporters in Arabidopsis.” <i>Plant Cell</i>, vol. 23, no. 5,
    American Society of Plant Biologists, 2011, pp. 1920–31, doi:<a href="https://doi.org/10.1105/tpc.111.083030">10.1105/tpc.111.083030</a>.
  short: S. Kitakura, S. Vanneste, S. Robert, C. Löfke, T. Teichmann, H. Tanaka, J.
    Friml, Plant Cell 23 (2011) 1920–1931.
date_created: 2018-12-11T12:01:18Z
date_published: 2011-05-01T00:00:00Z
date_updated: 2021-01-12T07:40:57Z
day: '01'
doi: 10.1105/tpc.111.083030
extern: 1
intvolume: '        23'
issue: '5'
month: '05'
page: 1920 - 1931
publication: Plant Cell
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '3614'
quality_controlled: 0
status: public
title: Clathrin mediates endocytosis and polar distribution of PIN auxin transporters
  in Arabidopsis
type: journal_article
volume: 23
year: '2011'
...
---
_id: '3088'
abstract:
- lang: eng
  text: 'Background: Whereas the majority of animals develop toward a predetermined
    body plan, plants show iterative growth and continually produce new organs and
    structures from actively dividing meristems. This raises an intriguing question:
    How are these newly developed organs patterned? In Arabidopsis embryos, radial
    symmetry is broken by the bisymmetric specification of the cotyledons in the apical
    domain. Subsequently, this bisymmetry is propagated to the root promeristem. Results:
    Here we present a mutually inhibitory feedback loop between auxin and cytokinin
    that sets distinct boundaries of hormonal output. Cytokinins promote the bisymmetric
    distribution of the PIN-FORMED (PIN) auxin efflux proteins, which channel auxin
    toward a central domain. High auxin promotes transcription of the cytokinin signaling
    inhibitor AHP6, which closes the interaction loop. This bisymmetric auxin response
    domain specifies the differentiation of protoxylem in a bisymmetric pattern. In
    embryonic roots, cytokinin is required to translate a bisymmetric auxin response
    in the cotyledons to a bisymmetric vascular pattern in the root promeristem. Conclusions:
    Our results present an interactive feedback loop between hormonal signaling and
    transport by which small biases in hormonal input are propagated into distinct
    signaling domains to specify the vascular pattern in the root meristem. It is
    an intriguing possibility that such a mechanism could transform radial patterns
    and allow continuous vascular connections between other newly emerging organs.'
author:
- first_name: Anthony
  full_name: Bishopp, Anthony
  last_name: Bishopp
- first_name: Hanna
  full_name: Help, Hanna
  last_name: Help
- first_name: Sedeer
  full_name: El-Showk, Sedeer
  last_name: El Showk
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
- first_name: Ben
  full_name: Scheres, Ben
  last_name: Scheres
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Ari
  full_name: Mähönen, Ari Pekka
  last_name: Mähönen
- first_name: Ykä
  full_name: Helariutta, Ykä
  last_name: Helariutta
citation:
  ama: Bishopp A, Help H, El Showk S, et al. A mutually inhibitory interaction between
    auxin and cytokinin specifies vascular pattern in roots. <i>Current Biology</i>.
    2011;21(11):917-926. doi:<a href="https://doi.org/10.1016/j.cub.2011.04.017">10.1016/j.cub.2011.04.017</a>
  apa: Bishopp, A., Help, H., El Showk, S., Weijers, D., Scheres, B., Friml, J., …
    Helariutta, Y. (2011). A mutually inhibitory interaction between auxin and cytokinin
    specifies vascular pattern in roots. <i>Current Biology</i>. Cell Press. <a href="https://doi.org/10.1016/j.cub.2011.04.017">https://doi.org/10.1016/j.cub.2011.04.017</a>
  chicago: Bishopp, Anthony, Hanna Help, Sedeer El Showk, Dolf Weijers, Ben Scheres,
    Jiří Friml, Eva Benková, Ari Mähönen, and Ykä Helariutta. “A Mutually Inhibitory
    Interaction between Auxin and Cytokinin Specifies Vascular Pattern in Roots.”
    <i>Current Biology</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.cub.2011.04.017">https://doi.org/10.1016/j.cub.2011.04.017</a>.
  ieee: A. Bishopp <i>et al.</i>, “A mutually inhibitory interaction between auxin
    and cytokinin specifies vascular pattern in roots,” <i>Current Biology</i>, vol.
    21, no. 11. Cell Press, pp. 917–926, 2011.
  ista: Bishopp A, Help H, El Showk S, Weijers D, Scheres B, Friml J, Benková E, Mähönen
    A, Helariutta Y. 2011. A mutually inhibitory interaction between auxin and cytokinin
    specifies vascular pattern in roots. Current Biology. 21(11), 917–926.
  mla: Bishopp, Anthony, et al. “A Mutually Inhibitory Interaction between Auxin and
    Cytokinin Specifies Vascular Pattern in Roots.” <i>Current Biology</i>, vol. 21,
    no. 11, Cell Press, 2011, pp. 917–26, doi:<a href="https://doi.org/10.1016/j.cub.2011.04.017">10.1016/j.cub.2011.04.017</a>.
  short: A. Bishopp, H. Help, S. El Showk, D. Weijers, B. Scheres, J. Friml, E. Benková,
    A. Mähönen, Y. Helariutta, Current Biology 21 (2011) 917–926.
date_created: 2018-12-11T12:01:18Z
date_published: 2011-06-07T00:00:00Z
date_updated: 2021-01-12T07:40:58Z
day: '07'
doi: 10.1016/j.cub.2011.04.017
extern: 1
intvolume: '        21'
issue: '11'
month: '06'
page: 917 - 926
publication: Current Biology
publication_status: published
publisher: Cell Press
publist_id: '3613'
quality_controlled: 0
status: public
title: A mutually inhibitory interaction between auxin and cytokinin specifies vascular
  pattern in roots
type: journal_article
volume: 21
year: '2011'
...
---
_id: '3089'
abstract:
- lang: eng
  text: The phytohormone auxin is an important determinant of plant development. Directional
    auxin flow within tissues depends on polar localization of PIN auxin transporters.
    To explore regulation of PIN-mediated auxin transport, we screened for suppressors
    of PIN1 overexpression (supo) and identified an inositol polyphosphate 1-phosphatase
    mutant (supo1), with elevated inositol trisphosphate (InsP 3) and cytosolic Ca
    2+ levels. Pharmacological and genetic increases in InsP 3 or Ca 2+ levels also
    suppressed the PIN1 gain-of-function phenotypes and caused defects in basal PIN
    localization, auxin transport and auxin-mediated development. In contrast, the
    reductions in InsP 3 levels and Ca 2+ signaling antagonized the effects of the
    supo1 mutation and disrupted preferentially apical PIN localization. InsP 3 and
    Ca 2+ are evolutionarily conserved second messengers involved in various cellular
    functions, particularly stress responses. Our findings implicate them as modifiers
    of cell polarity and polar auxin transport, and highlight a potential integration
    point through which Ca 2+ signaling-related stimuli could influence auxin-mediated
    development.
author:
- first_name: Jing
  full_name: Zhang, Jing
  last_name: Zhang
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Philip
  full_name: Brewer, Philip B
  last_name: Brewer
- first_name: Marta
  full_name: Michniewicz, Marta
  last_name: Michniewicz
- first_name: Peter
  full_name: Peter Grones
  id: 399876EC-F248-11E8-B48F-1D18A9856A87
  last_name: Grones
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Christian
  full_name: Löfke, Christian
  last_name: Löfke
- first_name: Thomas
  full_name: Teichmann, Thomas
  last_name: Teichmann
- first_name: Agnieszka
  full_name: Bielach, Agnieszka
  last_name: Bielach
- first_name: Bernard
  full_name: Cannoot, Bernard
  last_name: Cannoot
- first_name: Klára
  full_name: Hoyerová, Klára
  last_name: Hoyerová
- first_name: Xu
  full_name: Xu Chen
  id: 4E5ADCAA-F248-11E8-B48F-1D18A9856A87
  last_name: Chen
- first_name: Hong
  full_name: Xue, Hong-Wei
  last_name: Xue
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Eva
  full_name: Zažímalová, Eva
  last_name: Zažímalová
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Zhang J, Vanneste S, Brewer P, et al. Inositol trisphosphate-induced ca^2+
    signaling modulates auxin transport and pin polarity. <i>Developmental Cell</i>.
    2011;20(6):855-866. doi:<a href="https://doi.org/10.1016/j.devcel.2011.05.013">10.1016/j.devcel.2011.05.013</a>
  apa: Zhang, J., Vanneste, S., Brewer, P., Michniewicz, M., Grones, P., Kleine Vehn,
    J., … Friml, J. (2011). Inositol trisphosphate-induced ca^2+ signaling modulates
    auxin transport and pin polarity. <i>Developmental Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.devcel.2011.05.013">https://doi.org/10.1016/j.devcel.2011.05.013</a>
  chicago: Zhang, Jing, Steffen Vanneste, Philip Brewer, Marta Michniewicz, Peter
    Grones, Jürgen Kleine Vehn, Christian Löfke, et al. “Inositol Trisphosphate-Induced
    Ca^2+ Signaling Modulates Auxin Transport and Pin Polarity.” <i>Developmental
    Cell</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.devcel.2011.05.013">https://doi.org/10.1016/j.devcel.2011.05.013</a>.
  ieee: J. Zhang <i>et al.</i>, “Inositol trisphosphate-induced ca^2+ signaling modulates
    auxin transport and pin polarity,” <i>Developmental Cell</i>, vol. 20, no. 6.
    Cell Press, pp. 855–866, 2011.
  ista: Zhang J, Vanneste S, Brewer P, Michniewicz M, Grones P, Kleine Vehn J, Löfke
    C, Teichmann T, Bielach A, Cannoot B, Hoyerová K, Chen X, Xue H, Benková E, Zažímalová
    E, Friml J. 2011. Inositol trisphosphate-induced ca^2+ signaling modulates auxin
    transport and pin polarity. Developmental Cell. 20(6), 855–866.
  mla: Zhang, Jing, et al. “Inositol Trisphosphate-Induced Ca^2+ Signaling Modulates
    Auxin Transport and Pin Polarity.” <i>Developmental Cell</i>, vol. 20, no. 6,
    Cell Press, 2011, pp. 855–66, doi:<a href="https://doi.org/10.1016/j.devcel.2011.05.013">10.1016/j.devcel.2011.05.013</a>.
  short: J. Zhang, S. Vanneste, P. Brewer, M. Michniewicz, P. Grones, J. Kleine Vehn,
    C. Löfke, T. Teichmann, A. Bielach, B. Cannoot, K. Hoyerová, X. Chen, H. Xue,
    E. Benková, E. Zažímalová, J. Friml, Developmental Cell 20 (2011) 855–866.
date_created: 2018-12-11T12:01:18Z
date_published: 2011-06-14T00:00:00Z
date_updated: 2021-01-12T07:40:58Z
day: '14'
doi: 10.1016/j.devcel.2011.05.013
extern: 1
intvolume: '        20'
issue: '6'
month: '06'
page: 855 - 866
publication: Developmental Cell
publication_status: published
publisher: Cell Press
publist_id: '3612'
quality_controlled: 0
status: public
title: Inositol trisphosphate-induced ca^2+ signaling modulates auxin transport and
  pin polarity
type: journal_article
volume: 20
year: '2011'
...
---
_id: '3090'
abstract:
- lang: eng
  text: The polarized transport of the phytohormone auxin [1], which is crucial for
    the regulation of different stages of plant development [2, 3], depends on the
    asymmetric plasma membrane distribution of the PIN-FORMED (PIN) auxin efflux carriers
    [4, 5]. The PIN polar localization results from clathrin-mediated endocytosis
    (CME) from the plasma membrane and subsequent polar recycling [6]. The Arabidopsis
    genome encodes two groups of dynamin-related proteins (DRPs) that show homology
    to mammalian dynamin - a protein required for fission of endocytic vesicles during
    CME [7, 8]. Here we show by coimmunoprecipitation (coIP), bimolecular fluorescence
    complementation (BiFC), and Förster resonance energy transfer (FRET) that members
    of the DRP1 group closely associate with PIN proteins at the cell plate. Localization
    and phenotypic analysis of novel drp1 mutants revealed a requirement for DRP1
    function in correct PIN distribution and in auxin-mediated development. We propose
    that rapid and specific internalization of PIN proteins mediated by the DRP1 proteins
    and the associated CME machinery from the cell plate membranes during cytokinesis
    is an important mechanism for proper polar PIN positioning in interphase cells.
author:
- first_name: Jozef
  full_name: Mravec, Jozef
  last_name: Mravec
- first_name: Jan
  full_name: Petrášek, Jan
  last_name: Petrášek
- first_name: Na
  full_name: Li, Na
  last_name: Li
- first_name: Sjef
  full_name: Boeren, Sjef
  last_name: Boeren
- first_name: Rumyana
  full_name: Karlova, Rumyana
  last_name: Karlova
- first_name: Saeko
  full_name: Kitakura, Saeko
  last_name: Kitakura
- first_name: Markéta
  full_name: Pařezová, Markéta
  last_name: Pařezová
- first_name: Satoshi
  full_name: Naramoto, Satoshi
  last_name: Naramoto
- first_name: Thomasz
  full_name: Nodzyński, Thomasz
  last_name: Nodzyński
- first_name: Pankaj
  full_name: Dhonukshe, Pankaj
  last_name: Dhonukshe
- first_name: Sebastian
  full_name: Bednarek, Sebastian Y
  last_name: Bednarek
- first_name: Eva
  full_name: Zažímalová, Eva
  last_name: Zažímalová
- first_name: Sacco
  full_name: De Vries, Sacco
  last_name: De Vries
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Mravec J, Petrášek J, Li N, et al. Cell plate restricted association of DRP1A
    and PIN proteins is required for cell polarity establishment in arabidopsis. <i>Current
    Biology</i>. 2011;21(12):1055-1060. doi:<a href="https://doi.org/10.1016/j.cub.2011.05.018">10.1016/j.cub.2011.05.018</a>
  apa: Mravec, J., Petrášek, J., Li, N., Boeren, S., Karlova, R., Kitakura, S., …
    Friml, J. (2011). Cell plate restricted association of DRP1A and PIN proteins
    is required for cell polarity establishment in arabidopsis. <i>Current Biology</i>.
    Cell Press. <a href="https://doi.org/10.1016/j.cub.2011.05.018">https://doi.org/10.1016/j.cub.2011.05.018</a>
  chicago: Mravec, Jozef, Jan Petrášek, Na Li, Sjef Boeren, Rumyana Karlova, Saeko
    Kitakura, Markéta Pařezová, et al. “Cell Plate Restricted Association of DRP1A
    and PIN Proteins Is Required for Cell Polarity Establishment in Arabidopsis.”
    <i>Current Biology</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.cub.2011.05.018">https://doi.org/10.1016/j.cub.2011.05.018</a>.
  ieee: J. Mravec <i>et al.</i>, “Cell plate restricted association of DRP1A and PIN
    proteins is required for cell polarity establishment in arabidopsis,” <i>Current
    Biology</i>, vol. 21, no. 12. Cell Press, pp. 1055–1060, 2011.
  ista: Mravec J, Petrášek J, Li N, Boeren S, Karlova R, Kitakura S, Pařezová M, Naramoto
    S, Nodzyński T, Dhonukshe P, Bednarek S, Zažímalová E, De Vries S, Friml J. 2011.
    Cell plate restricted association of DRP1A and PIN proteins is required for cell
    polarity establishment in arabidopsis. Current Biology. 21(12), 1055–1060.
  mla: Mravec, Jozef, et al. “Cell Plate Restricted Association of DRP1A and PIN Proteins
    Is Required for Cell Polarity Establishment in Arabidopsis.” <i>Current Biology</i>,
    vol. 21, no. 12, Cell Press, 2011, pp. 1055–60, doi:<a href="https://doi.org/10.1016/j.cub.2011.05.018">10.1016/j.cub.2011.05.018</a>.
  short: J. Mravec, J. Petrášek, N. Li, S. Boeren, R. Karlova, S. Kitakura, M. Pařezová,
    S. Naramoto, T. Nodzyński, P. Dhonukshe, S. Bednarek, E. Zažímalová, S. De Vries,
    J. Friml, Current Biology 21 (2011) 1055–1060.
date_created: 2018-12-11T12:01:19Z
date_published: 2011-06-21T00:00:00Z
date_updated: 2021-01-12T07:40:59Z
day: '21'
doi: 10.1016/j.cub.2011.05.018
extern: 1
intvolume: '        21'
issue: '12'
month: '06'
page: 1055 - 1060
publication: Current Biology
publication_status: published
publisher: Cell Press
publist_id: '3611'
quality_controlled: 0
status: public
title: Cell plate restricted association of DRP1A and PIN proteins is required for
  cell polarity establishment in arabidopsis
type: journal_article
volume: 21
year: '2011'
...
---
_id: '3091'
author:
- first_name: Michael
  full_name: Sauer, Michael
  last_name: Sauer
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Sauer M, Friml J. Fleeting hormone cues get stabilized for plant organogenesis.
    <i>Molecular Systems Biology</i>. 2011;7. doi:<a href="https://doi.org/10.1038/msb.2011.45">10.1038/msb.2011.45</a>
  apa: Sauer, M., &#38; Friml, J. (2011). Fleeting hormone cues get stabilized for
    plant organogenesis. <i>Molecular Systems Biology</i>. Nature Publishing Group.
    <a href="https://doi.org/10.1038/msb.2011.45">https://doi.org/10.1038/msb.2011.45</a>
  chicago: Sauer, Michael, and Jiří Friml. “Fleeting Hormone Cues Get Stabilized for
    Plant Organogenesis.” <i>Molecular Systems Biology</i>. Nature Publishing Group,
    2011. <a href="https://doi.org/10.1038/msb.2011.45">https://doi.org/10.1038/msb.2011.45</a>.
  ieee: M. Sauer and J. Friml, “Fleeting hormone cues get stabilized for plant organogenesis,”
    <i>Molecular Systems Biology</i>, vol. 7. Nature Publishing Group, 2011.
  ista: Sauer M, Friml J. 2011. Fleeting hormone cues get stabilized for plant organogenesis.
    Molecular Systems Biology. 7.
  mla: Sauer, Michael, and Jiří Friml. “Fleeting Hormone Cues Get Stabilized for Plant
    Organogenesis.” <i>Molecular Systems Biology</i>, vol. 7, Nature Publishing Group,
    2011, doi:<a href="https://doi.org/10.1038/msb.2011.45">10.1038/msb.2011.45</a>.
  short: M. Sauer, J. Friml, Molecular Systems Biology 7 (2011).
date_created: 2018-12-11T12:01:19Z
date_published: 2011-07-05T00:00:00Z
date_updated: 2021-01-12T07:41:00Z
day: '05'
doi: 10.1038/msb.2011.45
extern: '1'
external_id:
  pmid:
  - '21734646'
intvolume: '         7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159970/
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: Molecular Systems Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '3610'
quality_controlled: '1'
status: public
title: Fleeting hormone cues get stabilized for plant organogenesis
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2011'
...
---
_id: '3092'
abstract:
- lang: eng
  text: The phytohormone auxin is vital to plant growth and development. A unique
    property of auxin among all other plant hormones is its cell-to-cell polar transport
    that requires activity of polarly localized PIN-FORMED (PIN) auxin efflux transporters.
    Despite the substantial molecular insight into the cellular PIN polarization,
    the mechanistic understanding for developmentally and environmentally regulated
    PIN polarization is scarce. The long-standing belief that auxin modulates its
    own transport by means of a positive feedback mechanism has inspired both experimentalists
    and theoreticians for more than two decades. Recently, theoretical models for
    auxin-dependent patterning in plants include the feedback between auxin transport
    and the PIN protein localization. These computer models aid to assess the complexity
    of plant development by testing and predicting plausible scenarios for various
    developmental processes that occur in planta. Although the majority of these models
    rely on purely heuristic principles, the most recent mechanistic models tentatively
    integrate biologically testable components into known cellular processes that
    underlie the PIN polarity regulation. The existing and emerging computational
    approaches to describe PIN polarization are presented and discussed in the light
    of recent experimental data on the PIN polar targeting.
author:
- 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: Willy
  full_name: Govaerts, Willy
  last_name: Govaerts
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Jürgen
  full_name: Kleine Vehn, Jürgen
  last_name: Kleine Vehn
citation:
  ama: 'Wabnik KT, Govaerts W, Friml J, Kleine Vehn J. Feedback models for polarized
    auxin transport: An emerging trend. <i>Molecular BioSystems</i>. 2011;7(8):2352-2359.
    doi:<a href="https://doi.org/10.1039/c1mb05109a">10.1039/c1mb05109a</a>'
  apa: 'Wabnik, K. T., Govaerts, W., Friml, J., &#38; Kleine Vehn, J. (2011). Feedback
    models for polarized auxin transport: An emerging trend. <i>Molecular BioSystems</i>.
    Royal Society of Chemistry. <a href="https://doi.org/10.1039/c1mb05109a">https://doi.org/10.1039/c1mb05109a</a>'
  chicago: 'Wabnik, Krzysztof T, Willy Govaerts, Jiří Friml, and Jürgen Kleine Vehn.
    “Feedback Models for Polarized Auxin Transport: An Emerging Trend.” <i>Molecular
    BioSystems</i>. Royal Society of Chemistry, 2011. <a href="https://doi.org/10.1039/c1mb05109a">https://doi.org/10.1039/c1mb05109a</a>.'
  ieee: 'K. T. Wabnik, W. Govaerts, J. Friml, and J. Kleine Vehn, “Feedback models
    for polarized auxin transport: An emerging trend,” <i>Molecular BioSystems</i>,
    vol. 7, no. 8. Royal Society of Chemistry, pp. 2352–2359, 2011.'
  ista: 'Wabnik KT, Govaerts W, Friml J, Kleine Vehn J. 2011. Feedback models for
    polarized auxin transport: An emerging trend. Molecular BioSystems. 7(8), 2352–2359.'
  mla: 'Wabnik, Krzysztof T., et al. “Feedback Models for Polarized Auxin Transport:
    An Emerging Trend.” <i>Molecular BioSystems</i>, vol. 7, no. 8, Royal Society
    of Chemistry, 2011, pp. 2352–59, doi:<a href="https://doi.org/10.1039/c1mb05109a">10.1039/c1mb05109a</a>.'
  short: K.T. Wabnik, W. Govaerts, J. Friml, J. Kleine Vehn, Molecular BioSystems
    7 (2011) 2352–2359.
date_created: 2018-12-11T12:01:20Z
date_published: 2011-06-10T00:00:00Z
date_updated: 2021-01-12T07:41:00Z
day: '10'
doi: 10.1039/c1mb05109a
extern: '1'
external_id:
  pmid:
  - '21660355'
intvolume: '         7'
issue: '8'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pubmed/21660355
month: '06'
oa: 1
oa_version: Published Version
page: 2352 - 2359
pmid: 1
publication: Molecular BioSystems
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '3608'
quality_controlled: '1'
status: public
title: 'Feedback models for polarized auxin transport: An emerging trend'
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2011'
...
---
_id: '3093'
abstract:
- lang: eng
  text: |2-

    Plants take up iron from the soil using the IRON-REGULATED TRANSPORTER 1 (IRT1) high-affinity iron transporter at the root surface. Sophisticated regulatory mechanisms allow plants to tightly control the levels of IRT1, ensuring optimal absorption of essential but toxic iron. Here, we demonstrate that overexpression of Arabidopsis thaliana IRT1 leads to constitutive IRT1 protein accumulation, metal overload, and oxidative stress. IRT1 is unexpectedly found in trans-Golgi network/early endosomes of root hair cells, and its levels and localization are unaffected by iron nutrition. Using pharmacological approaches, we show that IRT1 cycles to the plasma membrane to perform iron and metal uptake at the cell surface and is sent to the vacuole for proper turnover. We also prove that IRT1 is monoubiquitinated on several cytosol-exposed residues in vivo and that mutation of two putative monoubiquitination target residues in IRT1 triggers stabilization at the plasma membrane and leads to extreme lethality. Together, these data suggest a model in which monoubiquitin-dependent internalization/sorting and turnover keep the plasma membrane pool of IRT1 low to ensure proper iron uptake and to prevent metal toxicity. More generally, our work demonstrates the existence of monoubiquitin-dependent trafficking to lytic vacuoles in plants and points to proteasome-independent turnover of plasma membrane proteins.
author:
- first_name: Marie
  full_name: Barberon, Marie
  last_name: Barberon
- first_name: Enric
  full_name: Zelazny, Enric
  last_name: Zelazny
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
- first_name: Geneviève
  full_name: Conéjéro, Geneviève
  last_name: Conéjéro
- first_name: Cathy
  full_name: Curie, Cathy
  last_name: Curie
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Grégory
  full_name: Vert, Grégory
  last_name: Vert
citation:
  ama: Barberon M, Zelazny E, Robert S, et al. Monoubiquitin dependent endocytosis
    of the Iron Regulated Transporter 1 IRT1 transporter controls iron uptake in plants.
    <i>PNAS</i>. 2011;108(32):E450-E458. doi:<a href="https://doi.org/10.1073/pnas.1100659108">10.1073/pnas.1100659108</a>
  apa: Barberon, M., Zelazny, E., Robert, S., Conéjéro, G., Curie, C., Friml, J.,
    &#38; Vert, G. (2011). Monoubiquitin dependent endocytosis of the Iron Regulated
    Transporter 1 IRT1 transporter controls iron uptake in plants. <i>PNAS</i>. National
    Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1100659108">https://doi.org/10.1073/pnas.1100659108</a>
  chicago: Barberon, Marie, Enric Zelazny, Stéphanie Robert, Geneviève Conéjéro, Cathy
    Curie, Jiří Friml, and Grégory Vert. “Monoubiquitin Dependent Endocytosis of the
    Iron Regulated Transporter 1 IRT1 Transporter Controls Iron Uptake in Plants.”
    <i>PNAS</i>. National Academy of Sciences, 2011. <a href="https://doi.org/10.1073/pnas.1100659108">https://doi.org/10.1073/pnas.1100659108</a>.
  ieee: M. Barberon <i>et al.</i>, “Monoubiquitin dependent endocytosis of the Iron
    Regulated Transporter 1 IRT1 transporter controls iron uptake in plants,” <i>PNAS</i>,
    vol. 108, no. 32. National Academy of Sciences, pp. E450–E458, 2011.
  ista: Barberon M, Zelazny E, Robert S, Conéjéro G, Curie C, Friml J, Vert G. 2011.
    Monoubiquitin dependent endocytosis of the Iron Regulated Transporter 1 IRT1 transporter
    controls iron uptake in plants. PNAS. 108(32), E450–E458.
  mla: Barberon, Marie, et al. “Monoubiquitin Dependent Endocytosis of the Iron Regulated
    Transporter 1 IRT1 Transporter Controls Iron Uptake in Plants.” <i>PNAS</i>, vol.
    108, no. 32, National Academy of Sciences, 2011, pp. E450–58, doi:<a href="https://doi.org/10.1073/pnas.1100659108">10.1073/pnas.1100659108</a>.
  short: M. Barberon, E. Zelazny, S. Robert, G. Conéjéro, C. Curie, J. Friml, G. Vert,
    PNAS 108 (2011) E450–E458.
date_created: 2018-12-11T12:01:20Z
date_published: 2011-08-09T00:00:00Z
date_updated: 2021-01-12T07:41:00Z
day: '09'
doi: 10.1073/pnas.1100659108
extern: 1
intvolume: '       108'
issue: '32'
month: '08'
page: E450 - E458
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3607'
quality_controlled: 0
status: public
title: Monoubiquitin dependent endocytosis of the Iron Regulated Transporter 1 IRT1
  transporter controls iron uptake in plants
type: journal_article
volume: 108
year: '2011'
...
---
_id: '3094'
abstract:
- lang: eng
  text: Summary Gravitropism aligns plant growth with gravity. It involves gravity
    perception and the asymmetric distribution of the phytohormone auxin. Here we
    provide insights into the mechanism for hypocotyl gravitropic growth. We show
    that the Arabidopsis thaliana PIN3 auxin transporter is required for the asymmetric
    auxin distribution for the gravitropic response. Gravistimulation polarizes PIN3
    to the bottom side of hypocotyl endodermal cells, which correlates with an increased
    auxin response at the lower hypocotyl side. Both PIN3 polarization and hypocotyl
    bending require the activity of the trafficking regulator GNOM and the protein
    kinase PINOID. Our data suggest that gravity-induced PIN3 polarization diverts
    the auxin flow to mediate the asymmetric distribution of auxin for gravitropic
    shoot bending.
author:
- first_name: Hana
  full_name: Rakusová, Hana
  last_name: Rakusová
- first_name: Javier
  full_name: Gallego-Bartolomé, Javier
  last_name: Gallego Bartolomé
- first_name: Marleen
  full_name: Vanstraelen, Marleen
  last_name: Vanstraelen
- first_name: Hélène
  full_name: Robert, Hélène S
  last_name: Robert
- first_name: David
  full_name: Alabadí, David
  last_name: Alabadí
- first_name: Miguel
  full_name: Blázquez, Miguel A
  last_name: Blázquez
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Rakusová H, Gallego Bartolomé J, Vanstraelen M, et al. Polarization of PIN3
    dependent auxin transport for hypocotyl gravitropic response in Arabidopsis thaliana.
    <i>Plant Journal</i>. 2011;67(5):817-826. doi:<a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">10.1111/j.1365-313X.2011.04636.x</a>
  apa: Rakusová, H., Gallego Bartolomé, J., Vanstraelen, M., Robert, H., Alabadí,
    D., Blázquez, M., … Friml, J. (2011). Polarization of PIN3 dependent auxin transport
    for hypocotyl gravitropic response in Arabidopsis thaliana. <i>Plant Journal</i>.
    Wiley-Blackwell. <a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">https://doi.org/10.1111/j.1365-313X.2011.04636.x</a>
  chicago: Rakusová, Hana, Javier Gallego Bartolomé, Marleen Vanstraelen, Hélène Robert,
    David Alabadí, Miguel Blázquez, Eva Benková, and Jiří Friml. “Polarization of
    PIN3 Dependent Auxin Transport for Hypocotyl Gravitropic Response in Arabidopsis
    Thaliana.” <i>Plant Journal</i>. Wiley-Blackwell, 2011. <a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">https://doi.org/10.1111/j.1365-313X.2011.04636.x</a>.
  ieee: H. Rakusová <i>et al.</i>, “Polarization of PIN3 dependent auxin transport
    for hypocotyl gravitropic response in Arabidopsis thaliana,” <i>Plant Journal</i>,
    vol. 67, no. 5. Wiley-Blackwell, pp. 817–826, 2011.
  ista: Rakusová H, Gallego Bartolomé J, Vanstraelen M, Robert H, Alabadí D, Blázquez
    M, Benková E, Friml J. 2011. Polarization of PIN3 dependent auxin transport for
    hypocotyl gravitropic response in Arabidopsis thaliana. Plant Journal. 67(5),
    817–826.
  mla: Rakusová, Hana, et al. “Polarization of PIN3 Dependent Auxin Transport for
    Hypocotyl Gravitropic Response in Arabidopsis Thaliana.” <i>Plant Journal</i>,
    vol. 67, no. 5, Wiley-Blackwell, 2011, pp. 817–26, doi:<a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">10.1111/j.1365-313X.2011.04636.x</a>.
  short: H. Rakusová, J. Gallego Bartolomé, M. Vanstraelen, H. Robert, D. Alabadí,
    M. Blázquez, E. Benková, J. Friml, Plant Journal 67 (2011) 817–826.
date_created: 2018-12-11T12:01:21Z
date_published: 2011-09-01T00:00:00Z
date_updated: 2021-01-12T07:41:01Z
day: '01'
doi: 10.1111/j.1365-313X.2011.04636.x
extern: 1
intvolume: '        67'
issue: '5'
month: '09'
page: 817 - 826
publication: Plant Journal
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3606'
quality_controlled: 0
status: public
title: Polarization of PIN3 dependent auxin transport for hypocotyl gravitropic response
  in Arabidopsis thaliana
type: journal_article
volume: 67
year: '2011'
...
---
_id: '3095'
abstract:
- lang: eng
  text: Root system architecture depends on lateral root (LR) initiation that takes
    place in a relatively narrow developmental window (DW). Here, we analyzed the
    role of auxin gradients established along the parent root in defining this DW
    for LR initiation. Correlations between auxin distribution and response, and spatiotemporal
    control of LR initiation were analyzed in Arabidopsis thaliana and tomato (Solanum
    lycopersicum). In both Arabidopsis and tomato roots, a well defined zone, where
    auxin content and response are minimal, demarcates the position of a DW for founder
    cell specification and LR initiation. We show that in the zone of auxin minimum
    pericycle cells have highest probability to become founder cells and that auxin
    perception via the TIR1/AFB pathway, and polar auxin transport, are essential
    for the establishment of this zone. Altogether, this study reveals that the same
    morphogen-like molecule, auxin, can act simultaneously as a morphogenetic trigger
    of LR founder cell identity and as a gradient-dependent signal defining positioning
    of the founder cell specification. This auxin minimum zone might represent an
    important control mechanism ensuring the LR initiation steadiness and the acropetal
    LR initiation pattern. © 2011 The Authors. New Phytologist © 2011 New Phytologist
    Trust.
author:
- first_name: Joseph
  full_name: Dubrovsky, Joseph G
  last_name: Dubrovsky
- first_name: Selene
  full_name: Napsucialy-Mendivil, Selene
  last_name: Napsucialy Mendivil
- first_name: Jérôme
  full_name: Duclercq, Jérôme
  last_name: Duclercq
- first_name: Yan
  full_name: Cheng, Yan
  last_name: Cheng
- first_name: Svetlana
  full_name: Shishkova, Svetlana O
  last_name: Shishkova
- first_name: Maria
  full_name: Ivanchenko, Maria G
  last_name: Ivanchenko
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Angus
  full_name: Murphy, Angus S
  last_name: Murphy
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
citation:
  ama: Dubrovsky J, Napsucialy Mendivil S, Duclercq J, et al. Auxin minimum defines
    a developmental window for lateral root initiation. <i>New Phytologist</i>. 2011;191(4):970-983.
    doi:<a href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x"> 10.1111/j.1469-8137.2011.03757.x</a>
  apa: Dubrovsky, J., Napsucialy Mendivil, S., Duclercq, J., Cheng, Y., Shishkova,
    S., Ivanchenko, M., … Benková, E. (2011). Auxin minimum defines a developmental
    window for lateral root initiation. <i>New Phytologist</i>. Wiley-Blackwell. <a
    href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x">https://doi.org/ 10.1111/j.1469-8137.2011.03757.x</a>
  chicago: Dubrovsky, Joseph, Selene Napsucialy Mendivil, Jérôme Duclercq, Yan Cheng,
    Svetlana Shishkova, Maria Ivanchenko, Jiří Friml, Angus Murphy, and Eva Benková.
    “Auxin Minimum Defines a Developmental Window for Lateral Root Initiation.” <i>New
    Phytologist</i>. Wiley-Blackwell, 2011. <a href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x">https://doi.org/
    10.1111/j.1469-8137.2011.03757.x</a>.
  ieee: J. Dubrovsky <i>et al.</i>, “Auxin minimum defines a developmental window
    for lateral root initiation,” <i>New Phytologist</i>, vol. 191, no. 4. Wiley-Blackwell,
    pp. 970–983, 2011.
  ista: Dubrovsky J, Napsucialy Mendivil S, Duclercq J, Cheng Y, Shishkova S, Ivanchenko
    M, Friml J, Murphy A, Benková E. 2011. Auxin minimum defines a developmental window
    for lateral root initiation. New Phytologist. 191(4), 970–983.
  mla: Dubrovsky, Joseph, et al. “Auxin Minimum Defines a Developmental Window for
    Lateral Root Initiation.” <i>New Phytologist</i>, vol. 191, no. 4, Wiley-Blackwell,
    2011, pp. 970–83, doi:<a href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x">
    10.1111/j.1469-8137.2011.03757.x</a>.
  short: J. Dubrovsky, S. Napsucialy Mendivil, J. Duclercq, Y. Cheng, S. Shishkova,
    M. Ivanchenko, J. Friml, A. Murphy, E. Benková, New Phytologist 191 (2011) 970–983.
date_created: 2018-12-11T12:01:21Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2021-01-12T07:41:01Z
day: '01'
doi: ' 10.1111/j.1469-8137.2011.03757.x'
extern: 1
intvolume: '       191'
issue: '4'
month: '01'
page: 970 - 983
publication: New Phytologist
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3605'
quality_controlled: 0
status: public
title: Auxin minimum defines a developmental window for lateral root initiation
type: journal_article
volume: 191
year: '2011'
...
---
_id: '3096'
abstract:
- lang: eng
  text: Carrier-dependent, intercellular auxin transport is central to the developmental
    patterning of higher plants (tracheophytes). The evolution of this polar auxin
    transport might be linked to the translocation of some PIN auxin efflux carriers
    from their presumably ancestral localization at the endoplasmic reticulum (ER)
    to the polar domains at the plasma membrane. Here we propose an eventually ancient
    mechanism of intercellular auxin distribution by ER-localized auxin transporters
    involving intracellular auxin retention and switch-like release from the ER. The
    proposed model integrates feedback circuits utilizing the conserved nuclear auxin
    signaling for the regulation of PIN transcription and a hypothetical ER-based
    signaling for the regulation of PIN-dependent transport activity at the ER. Computer
    simulations of the model revealed its plausibility for generating auxin channels
    and localized auxin maxima highlighting the possibility of this alternative mechanism
    for polar auxin transport.
author:
- 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: Jürgen
  full_name: Kleine Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Willy
  full_name: Govaerts, Willy
  last_name: Govaerts
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Wabnik KT, Kleine Vehn J, Govaerts W, Friml J. Prototype cell-to-cell auxin
    transport mechanism by intracellular auxin compartmentalization. <i>Trends in
    Plant Science</i>. 2011;16(9):468-475. doi:<a href="https://doi.org/10.1016/j.tplants.2011.05.002">10.1016/j.tplants.2011.05.002</a>
  apa: Wabnik, K. T., Kleine Vehn, J., Govaerts, W., &#38; Friml, J. (2011). Prototype
    cell-to-cell auxin transport mechanism by intracellular auxin compartmentalization.
    <i>Trends in Plant Science</i>. Cell Press. <a href="https://doi.org/10.1016/j.tplants.2011.05.002">https://doi.org/10.1016/j.tplants.2011.05.002</a>
  chicago: Wabnik, Krzysztof T, Jürgen Kleine Vehn, Willy Govaerts, and Jiří Friml.
    “Prototype Cell-to-Cell Auxin Transport Mechanism by Intracellular Auxin Compartmentalization.”
    <i>Trends in Plant Science</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.tplants.2011.05.002">https://doi.org/10.1016/j.tplants.2011.05.002</a>.
  ieee: K. T. Wabnik, J. Kleine Vehn, W. Govaerts, and J. Friml, “Prototype cell-to-cell
    auxin transport mechanism by intracellular auxin compartmentalization,” <i>Trends
    in Plant Science</i>, vol. 16, no. 9. Cell Press, pp. 468–475, 2011.
  ista: Wabnik KT, Kleine Vehn J, Govaerts W, Friml J. 2011. Prototype cell-to-cell
    auxin transport mechanism by intracellular auxin compartmentalization. Trends
    in Plant Science. 16(9), 468–475.
  mla: Wabnik, Krzysztof T., et al. “Prototype Cell-to-Cell Auxin Transport Mechanism
    by Intracellular Auxin Compartmentalization.” <i>Trends in Plant Science</i>,
    vol. 16, no. 9, Cell Press, 2011, pp. 468–75, doi:<a href="https://doi.org/10.1016/j.tplants.2011.05.002">10.1016/j.tplants.2011.05.002</a>.
  short: K.T. Wabnik, J. Kleine Vehn, W. Govaerts, J. Friml, Trends in Plant Science
    16 (2011) 468–475.
date_created: 2018-12-11T12:01:21Z
date_published: 2011-09-01T00:00:00Z
date_updated: 2021-01-12T07:41:01Z
day: '01'
doi: 10.1016/j.tplants.2011.05.002
extern: '1'
intvolume: '        16'
issue: '9'
language:
- iso: eng
month: '09'
oa_version: None
page: 468 - 475
publication: Trends in Plant Science
publication_status: published
publisher: Cell Press
publist_id: '3604'
quality_controlled: '1'
status: public
title: Prototype cell-to-cell auxin transport mechanism by intracellular auxin compartmentalization
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2011'
...
---
_id: '3097'
abstract:
- lang: eng
  text: Cytokinin is an important regulator of plant growth and development. In Arabidopsis
    thaliana, the two-component phosphorelay mediated through a family of histidine
    kinases and response regulators is recognized as the principal cytokinin signal
    transduction mechanism activating the complex transcriptional response to control
    various developmental processes. Here, we identified an alternative mode of cytokinin
    action that uses endocytic trafficking as a means to direct plant organogenesis.
    This activity occurs downstream of known cytokinin receptors but through a branch
    of the cytokinin signaling pathway that does not involve transcriptional regulation.
    We show that cytokinin regulates endocytic recycling of the auxin efflux carrier
    PINFORMED1 (PIN1) by redirecting it for lytic degradation in vacuoles. Stimulation
    of the lytic PIN1 degradation is not a default effect for general downregulation
    of proteins from plasma membranes, but a specific mechanism to rapidly modulate
    the auxin distribution in cytokinin-mediated developmental processes.
author:
- first_name: Peter
  full_name: Peter Marhavy
  id: 3F45B078-F248-11E8-B48F-1D18A9856A87
  last_name: Marhavy
  orcid: 0000-0001-5227-5741
- first_name: Agnieszka
  full_name: Bielach, Agnieszka
  last_name: Bielach
- first_name: Lindy
  full_name: Abas, Lindy
  last_name: Abas
- first_name: Anas
  full_name: Abuzeineh, Anas
  last_name: Abuzeineh
- first_name: Jérôme
  full_name: Duclercq, Jérôme
  last_name: Duclercq
- first_name: Hirokazu
  full_name: Tanaka, Hirokazu
  last_name: Tanaka
- first_name: Markéta
  full_name: Pařezová, Markéta
  last_name: Pařezová
- first_name: Jan
  full_name: Petrášek, Jan
  last_name: Petrášek
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
citation:
  ama: Marhavý P, Bielach A, Abas L, et al. Cytokinin modulates endocytic trafficking
    of PIN1 auxin efflux carrier to control plant organogenesis. <i>Developmental
    Cell</i>. 2011;21(4):796-804. doi:<a href="https://doi.org/10.1016/j.devcel.2011.08.014">10.1016/j.devcel.2011.08.014</a>
  apa: Marhavý, P., Bielach, A., Abas, L., Abuzeineh, A., Duclercq, J., Tanaka, H.,
    … Benková, E. (2011). Cytokinin modulates endocytic trafficking of PIN1 auxin
    efflux carrier to control plant organogenesis. <i>Developmental Cell</i>. Cell
    Press. <a href="https://doi.org/10.1016/j.devcel.2011.08.014">https://doi.org/10.1016/j.devcel.2011.08.014</a>
  chicago: Marhavý, Peter, Agnieszka Bielach, Lindy Abas, Anas Abuzeineh, Jérôme Duclercq,
    Hirokazu Tanaka, Markéta Pařezová, et al. “Cytokinin Modulates Endocytic Trafficking
    of PIN1 Auxin Efflux Carrier to Control Plant Organogenesis.” <i>Developmental
    Cell</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.devcel.2011.08.014">https://doi.org/10.1016/j.devcel.2011.08.014</a>.
  ieee: P. Marhavý <i>et al.</i>, “Cytokinin modulates endocytic trafficking of PIN1
    auxin efflux carrier to control plant organogenesis,” <i>Developmental Cell</i>,
    vol. 21, no. 4. Cell Press, pp. 796–804, 2011.
  ista: Marhavý P, Bielach A, Abas L, Abuzeineh A, Duclercq J, Tanaka H, Pařezová
    M, Petrášek J, Friml J, Kleine Vehn J, Benková E. 2011. Cytokinin modulates endocytic
    trafficking of PIN1 auxin efflux carrier to control plant organogenesis. Developmental
    Cell. 21(4), 796–804.
  mla: Marhavý, Peter, et al. “Cytokinin Modulates Endocytic Trafficking of PIN1 Auxin
    Efflux Carrier to Control Plant Organogenesis.” <i>Developmental Cell</i>, vol.
    21, no. 4, Cell Press, 2011, pp. 796–804, doi:<a href="https://doi.org/10.1016/j.devcel.2011.08.014">10.1016/j.devcel.2011.08.014</a>.
  short: P. Marhavý, A. Bielach, L. Abas, A. Abuzeineh, J. Duclercq, H. Tanaka, M.
    Pařezová, J. Petrášek, J. Friml, J. Kleine Vehn, E. Benková, Developmental Cell
    21 (2011) 796–804.
date_created: 2018-12-11T12:01:22Z
date_published: 2011-10-18T00:00:00Z
date_updated: 2021-01-12T07:41:02Z
day: '18'
doi: 10.1016/j.devcel.2011.08.014
extern: 1
intvolume: '        21'
issue: '4'
month: '10'
page: 796 - 804
publication: Developmental Cell
publication_status: published
publisher: Cell Press
publist_id: '3603'
quality_controlled: 0
status: public
title: Cytokinin modulates endocytic trafficking of PIN1 auxin efflux carrier to control
  plant organogenesis
type: journal_article
volume: 21
year: '2011'
...
---
_id: '3098'
abstract:
- lang: eng
  text: Cell polarity reflected by asymmetric distribution of proteins at the plasma
    membrane is a fundamental feature of unicellular and multicellular organisms.
    It remains conceptually unclear how cell polarity is kept in cell wall-encapsulated
    plant cells. We have used super-resolution and semi-quantitative live-cell imaging
    in combination with pharmacological, genetic, and computational approaches to
    reveal insights into the mechanism of cell polarity maintenance in Arabidopsis
    thaliana. We show that polar-competent PIN transporters for the phytohormone auxin
    are delivered to the center of polar domains by super-polar recycling. Within
    the plasma membrane, PINs are recruited into non-mobile membrane clusters and
    their lateral diffusion is dramatically reduced, which ensures longer polar retention.
    At the circumventing edges of the polar domain, spatially defined internalization
    of escaped cargos occurs by clathrin-dependent endocytosis. Computer simulations
    confirm that the combination of these processes provides a robust mechanism for
    polarity maintenance in plant cells. Moreover, our study suggests that the regulation
    of lateral diffusion and spatially defined endocytosis, but not super-polar exocytosis
    have primary importance for PIN polarity maintenance.
author:
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Krzysztof T
  full_name: Krzysztof Wabnik
  id: 4DE369A4-F248-11E8-B48F-1D18A9856A87
  last_name: Wabnik
  orcid: 0000-0001-7263-0560
- first_name: Alexandre
  full_name: Martinière, Alexandre
  last_name: Martinière
- first_name: Łukasz
  full_name: Łangowski, Łukasz
  last_name: Łangowski
- first_name: Katrin
  full_name: Willig, Katrin
  last_name: Willig
- first_name: Satoshi
  full_name: Naramoto, Satoshi
  last_name: Naramoto
- first_name: Johannes
  full_name: Leitner, Johannes
  last_name: Leitner
- first_name: Hirokazu
  full_name: Tanaka, Hirokazu
  last_name: Tanaka
- first_name: Stefan
  full_name: Jakobs, Stefan
  last_name: Jakobs
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
- first_name: Christian
  full_name: Luschnig, Christian
  last_name: Luschnig
- first_name: Willy
  full_name: Govaerts, Willy J
  last_name: Govaerts
- first_name: Stefan
  full_name: Hell, Stefan W
  last_name: Hell
- first_name: John
  full_name: Runions, John
  last_name: Runions
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Kleine Vehn J, Wabnik KT, Martinière A, et al. Recycling, clustering and endocytosis
    jointly maintain PIN auxin carrier polarity at the plasma membrane. <i>Molecular
    Systems Biology</i>. 2011;7. doi:<a href="https://doi.org/10.1038/msb.2011.72">10.1038/msb.2011.72</a>
  apa: Kleine Vehn, J., Wabnik, K. T., Martinière, A., Łangowski, Ł., Willig, K.,
    Naramoto, S., … Friml, J. (2011). Recycling, clustering and endocytosis jointly
    maintain PIN auxin carrier polarity at the plasma membrane. <i>Molecular Systems
    Biology</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/msb.2011.72">https://doi.org/10.1038/msb.2011.72</a>
  chicago: Kleine Vehn, Jürgen, Krzysztof T Wabnik, Alexandre Martinière, Łukasz Łangowski,
    Katrin Willig, Satoshi Naramoto, Johannes Leitner, et al. “Recycling, Clustering
    and Endocytosis Jointly Maintain PIN Auxin Carrier Polarity at the Plasma Membrane.”
    <i>Molecular Systems Biology</i>. Nature Publishing Group, 2011. <a href="https://doi.org/10.1038/msb.2011.72">https://doi.org/10.1038/msb.2011.72</a>.
  ieee: J. Kleine Vehn <i>et al.</i>, “Recycling, clustering and endocytosis jointly
    maintain PIN auxin carrier polarity at the plasma membrane,” <i>Molecular Systems
    Biology</i>, vol. 7. Nature Publishing Group, 2011.
  ista: Kleine Vehn J, Wabnik KT, Martinière A, Łangowski Ł, Willig K, Naramoto S,
    Leitner J, Tanaka H, Jakobs S, Robert S, Luschnig C, Govaerts W, Hell S, Runions
    J, Friml J. 2011. Recycling, clustering and endocytosis jointly maintain PIN auxin
    carrier polarity at the plasma membrane. Molecular Systems Biology. 7.
  mla: Kleine Vehn, Jürgen, et al. “Recycling, Clustering and Endocytosis Jointly
    Maintain PIN Auxin Carrier Polarity at the Plasma Membrane.” <i>Molecular Systems
    Biology</i>, vol. 7, Nature Publishing Group, 2011, doi:<a href="https://doi.org/10.1038/msb.2011.72">10.1038/msb.2011.72</a>.
  short: J. Kleine Vehn, K.T. Wabnik, A. Martinière, Ł. Łangowski, K. Willig, S. Naramoto,
    J. Leitner, H. Tanaka, S. Jakobs, S. Robert, C. Luschnig, W. Govaerts, S. Hell,
    J. Runions, J. Friml, Molecular Systems Biology 7 (2011).
date_created: 2018-12-11T12:01:22Z
date_published: 2011-10-25T00:00:00Z
date_updated: 2021-01-12T07:41:02Z
day: '25'
doi: 10.1038/msb.2011.72
extern: 1
intvolume: '         7'
month: '10'
publication: Molecular Systems Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '3601'
quality_controlled: 0
status: public
title: Recycling, clustering and endocytosis jointly maintain PIN auxin carrier polarity
  at the plasma membrane
type: journal_article
volume: 7
year: '2011'
...
---
_id: '3099'
abstract:
- lang: eng
  text: Endomembrane trafficking relies on the coordination of a highly complex, dynamic
    network of intracellular vesicles. Understanding the network will require a dissection
    of cargo and vesicle dynamics at the cellular level in vivo. This is also a key
    to establishing a link between vesicular networks and their functional roles in
    development. We used a high-content intracellular screen to discover small molecules
    targeting endomembrane trafficking in vivo in a complex eukaryote, Arabidopsis
    thaliana. Tens of thousands of molecules were prescreened and a selected subset
    was interrogated against a panel of plasma membrane (PM) and other endomembrane
    compartment markers to identify molecules that altered vesicle trafficking. The
    extensive image dataset was transformed by a flexible algorithm into a marker-by-phenotype-by-treatment
    time matrix and revealed groups of molecules that induced similar subcellular
    fingerprints (clusters). This matrix provides a platform for a systems view of
    trafficking. Molecules from distinct clusters presented avenues and enabled an
    entry point to dissect recycling at the PM, vacuolar sorting, and cell-plate maturation.
    Bioactivity in human cells indicated the value of the approach to identifying
    small molecules that are active in diverse organisms for biology and drug discovery.
author:
- first_name: Georgia
  full_name: Drakakaki, Georgia
  last_name: Drakakaki
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
- first_name: Anna
  full_name: Szatmári, Anna-Maria
  last_name: Szatmári
- first_name: Michelle
  full_name: Brown, Michelle Q
  last_name: Brown
- first_name: Shingo
  full_name: Nagawa, Shingo
  last_name: Nagawa
- first_name: Daniël
  full_name: Van Damme, Daniël
  last_name: Van Damme
- first_name: Marylin
  full_name: Leonard, Marylin
  last_name: Leonard
- first_name: Zhenbiao
  full_name: Yang, Zhenbiao
  last_name: Yang
- first_name: Thomas
  full_name: Girke, Thomas
  last_name: Girke
- first_name: Sandra
  full_name: Schmid, Sandra L
  last_name: Schmid
- first_name: Eugenia
  full_name: Russinova, Eugenia
  last_name: Russinova
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Natasha
  full_name: Raikhel, Natasha V
  last_name: Raikhel
- first_name: Glen
  full_name: Hicks, Glen R
  last_name: Hicks
citation:
  ama: Drakakaki G, Robert S, Szatmári A, et al. Clusters of bioactive compounds target
    dynamic endomembrane networks in vivo. <i>PNAS</i>. 2011;108(43):17850-17855.
    doi:<a href="https://doi.org/10.1073/pnas.1108581108">10.1073/pnas.1108581108</a>
  apa: Drakakaki, G., Robert, S., Szatmári, A., Brown, M., Nagawa, S., Van Damme,
    D., … Hicks, G. (2011). Clusters of bioactive compounds target dynamic endomembrane
    networks in vivo. <i>PNAS</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1108581108">https://doi.org/10.1073/pnas.1108581108</a>
  chicago: Drakakaki, Georgia, Stéphanie Robert, Anna Szatmári, Michelle Brown, Shingo
    Nagawa, Daniël Van Damme, Marylin Leonard, et al. “Clusters of Bioactive Compounds
    Target Dynamic Endomembrane Networks in Vivo.” <i>PNAS</i>. National Academy of
    Sciences, 2011. <a href="https://doi.org/10.1073/pnas.1108581108">https://doi.org/10.1073/pnas.1108581108</a>.
  ieee: G. Drakakaki <i>et al.</i>, “Clusters of bioactive compounds target dynamic
    endomembrane networks in vivo,” <i>PNAS</i>, vol. 108, no. 43. National Academy
    of Sciences, pp. 17850–17855, 2011.
  ista: Drakakaki G, Robert S, Szatmári A, Brown M, Nagawa S, Van Damme D, Leonard
    M, Yang Z, Girke T, Schmid S, Russinova E, Friml J, Raikhel N, Hicks G. 2011.
    Clusters of bioactive compounds target dynamic endomembrane networks in vivo.
    PNAS. 108(43), 17850–17855.
  mla: Drakakaki, Georgia, et al. “Clusters of Bioactive Compounds Target Dynamic
    Endomembrane Networks in Vivo.” <i>PNAS</i>, vol. 108, no. 43, National Academy
    of Sciences, 2011, pp. 17850–55, doi:<a href="https://doi.org/10.1073/pnas.1108581108">10.1073/pnas.1108581108</a>.
  short: G. Drakakaki, S. Robert, A. Szatmári, M. Brown, S. Nagawa, D. Van Damme,
    M. Leonard, Z. Yang, T. Girke, S. Schmid, E. Russinova, J. Friml, N. Raikhel,
    G. Hicks, PNAS 108 (2011) 17850–17855.
date_created: 2018-12-11T12:01:23Z
date_published: 2011-10-25T00:00:00Z
date_updated: 2021-01-12T07:41:02Z
day: '25'
doi: 10.1073/pnas.1108581108
extern: 1
intvolume: '       108'
issue: '43'
month: '10'
page: 17850 - 17855
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3602'
quality_controlled: 0
status: public
title: Clusters of bioactive compounds target dynamic endomembrane networks in vivo
type: journal_article
volume: 108
year: '2011'
...
---
_id: '3100'
abstract:
- lang: eng
  text: In multicellular organisms, morphogenesis relies on a strict coordination
    in time and space of cell proliferation and differentiation. In contrast to animals,
    plant development displays continuous organ formation and adaptive growth responses
    during their lifespan relying on a tight coordination of cell proliferation. How
    developmental signals interact with the plant cell-cycle machinery is largely
    unknown. Here, we characterize plant A2-type cyclins, a small gene family of mitotic
    cyclins, and show how they contribute to the fine-tuning of local proliferation
    during plant development. Moreover, the timely repression of CYCA2;3 expression
    in newly formed guard cells is shown to require the stomatal transcription factors
    FOUR LIPS/MYB124 and MYB88, providing a direct link between developmental programming
    and cell-cycle exit in plants. Thus, transcriptional downregulation of CYCA2s
    represents a critical mechanism to coordinate proliferation during plant development.
author:
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Frederik
  full_name: Coppens, Frederik
  last_name: Coppens
- first_name: Eunkyoung
  full_name: Lee, EunKyoung
  last_name: Lee
- first_name: Tyler
  full_name: Donner, Tyler J
  last_name: Donner
- first_name: Zidian
  full_name: Xie, Zidian
  last_name: Xie
- first_name: Gert
  full_name: Van Isterdael, Gert
  last_name: Van Isterdael
- first_name: Stijn
  full_name: Dhondt, Stijn
  last_name: Dhondt
- first_name: Freya
  full_name: De Winter, Freya
  last_name: De Winter
- first_name: Bert
  full_name: De Rybel, Bert
  last_name: De Rybel
- first_name: Marnik
  full_name: Vuylsteke, Marnik
  last_name: Vuylsteke
- first_name: Lieven
  full_name: De Veylder, Lieven
  last_name: De Veylder
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Dirk
  full_name: Inzé, Dirk
  last_name: Inzé
- first_name: Erich
  full_name: Grotewold, Erich
  last_name: Grotewold
- first_name: Enrico
  full_name: Scarpella, Enrico
  last_name: Scarpella
- first_name: Fred
  full_name: Sack, Fred
  last_name: Sack
- first_name: Gerrit
  full_name: Beemster, Gerrit T
  last_name: Beemster
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
citation:
  ama: Vanneste S, Coppens F, Lee E, et al. Developmental regulation of CYCA2s contributes
    to tissue-specific proliferation in Arabidopsis . <i>EMBO Journal</i>. 2011;30(16):3430-3441.
    doi:<a href="https://doi.org/10.1038/emboj.2011.240">10.1038/emboj.2011.240</a>
  apa: Vanneste, S., Coppens, F., Lee, E., Donner, T., Xie, Z., Van Isterdael, G.,
    … Beeckman, T. (2011). Developmental regulation of CYCA2s contributes to tissue-specific
    proliferation in Arabidopsis . <i>EMBO Journal</i>. Wiley-Blackwell. <a href="https://doi.org/10.1038/emboj.2011.240">https://doi.org/10.1038/emboj.2011.240</a>
  chicago: Vanneste, Steffen, Frederik Coppens, Eunkyoung Lee, Tyler Donner, Zidian
    Xie, Gert Van Isterdael, Stijn Dhondt, et al. “Developmental Regulation of CYCA2s
    Contributes to Tissue-Specific Proliferation in Arabidopsis .” <i>EMBO Journal</i>.
    Wiley-Blackwell, 2011. <a href="https://doi.org/10.1038/emboj.2011.240">https://doi.org/10.1038/emboj.2011.240</a>.
  ieee: S. Vanneste <i>et al.</i>, “Developmental regulation of CYCA2s contributes
    to tissue-specific proliferation in Arabidopsis ,” <i>EMBO Journal</i>, vol. 30,
    no. 16. Wiley-Blackwell, pp. 3430–3441, 2011.
  ista: Vanneste S, Coppens F, Lee E, Donner T, Xie Z, Van Isterdael G, Dhondt S,
    De Winter F, De Rybel B, Vuylsteke M, De Veylder L, Friml J, Inzé D, Grotewold
    E, Scarpella E, Sack F, Beemster G, Beeckman T. 2011. Developmental regulation
    of CYCA2s contributes to tissue-specific proliferation in Arabidopsis . EMBO Journal.
    30(16), 3430–3441.
  mla: Vanneste, Steffen, et al. “Developmental Regulation of CYCA2s Contributes to
    Tissue-Specific Proliferation in Arabidopsis .” <i>EMBO Journal</i>, vol. 30,
    no. 16, Wiley-Blackwell, 2011, pp. 3430–41, doi:<a href="https://doi.org/10.1038/emboj.2011.240">10.1038/emboj.2011.240</a>.
  short: S. Vanneste, F. Coppens, E. Lee, T. Donner, Z. Xie, G. Van Isterdael, S.
    Dhondt, F. De Winter, B. De Rybel, M. Vuylsteke, L. De Veylder, J. Friml, D. Inzé,
    E. Grotewold, E. Scarpella, F. Sack, G. Beemster, T. Beeckman, EMBO Journal 30
    (2011) 3430–3441.
date_created: 2018-12-11T12:01:23Z
date_published: 2011-08-17T00:00:00Z
date_updated: 2021-01-12T07:41:04Z
day: '17'
doi: 10.1038/emboj.2011.240
extern: 1
intvolume: '        30'
issue: '16'
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160660/
month: '08'
oa: 1
page: 3430 - 3441
publication: EMBO Journal
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3600'
quality_controlled: 0
status: public
title: 'Developmental regulation of CYCA2s contributes to tissue-specific proliferation
  in Arabidopsis '
type: journal_article
volume: 30
year: '2011'
...
---
_id: '3101'
abstract:
- lang: eng
  text: Subcellular trafficking is required for a multitude of functions in eukaryotic
    cells. It involves regulation of cargo sorting, vesicle formation, trafficking
    and fusion processes at multiple levels. Adaptor protein (AP) complexes are key
    regulators of cargo sorting into vesicles in yeast and mammals but their existence
    and function in plants have not been demonstrated. Here we report the identification
    of the protein-affected trafficking 4 (pat4) mutant defective in the putative
    δ subunit of the AP-3 complex. pat4 and pat2, a mutant isolated from the same
    GFP imaging-based forward genetic screen that lacks a functional putative AP-3
    β, as well as dominant negative AP-3 μ transgenic lines display undistinguishable
    phenotypes characterized by largely normal morphology and development, but strong
    intracellular accumulation of membrane proteins in aberrant vacuolar structures.
    All mutants are defective in morphology and function of lytic and protein storage
    vacuoles (PSVs) but show normal sorting of reserve proteins to PSVs. Immunoprecipitation
    experiments and genetic studies revealed tight functional and physical associations
    of putative AP-3 β and AP-3 δ subunits. Furthermore, both proteins are closely
    linked with putative AP-3 μ and σ subunits and several components of the clathrin
    and dynamin machineries. Taken together, these results demonstrate that AP complexes,
    similar to those in other eukaryotes, exist in plants, and that AP-3 plays a specific
    role in the regulation of biogenesis and function of vacuoles in plant cells.
    © 2011 IBCB, SIBS, CAS All rights reserved
author:
- first_name: Marta
  full_name: Zwiewka, Marta
  last_name: Zwiewka
- first_name: Elena
  full_name: Feraru, Elena
  last_name: Feraru
- first_name: Barbara
  full_name: Möller, Barbara
  last_name: Möller
- first_name: Inhwan
  full_name: Hwang, Inhwan
  last_name: Hwang
- first_name: Mugurel
  full_name: Feraru, Mugurel I
  last_name: Feraru
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Zwiewka M, Feraru E, Möller B, et al. The AP 3 adaptor complex is required
    for vacuolar function in Arabidopsis. <i>Cell Research</i>. 2011;21(12):1711-1722.
    doi:<a href="https://doi.org/10.1038/cr.2011.99">10.1038/cr.2011.99</a>
  apa: Zwiewka, M., Feraru, E., Möller, B., Hwang, I., Feraru, M., Kleine Vehn, J.,
    … Friml, J. (2011). The AP 3 adaptor complex is required for vacuolar function
    in Arabidopsis. <i>Cell Research</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/cr.2011.99">https://doi.org/10.1038/cr.2011.99</a>
  chicago: Zwiewka, Marta, Elena Feraru, Barbara Möller, Inhwan Hwang, Mugurel Feraru,
    Jürgen Kleine Vehn, Dolf Weijers, and Jiří Friml. “The AP 3 Adaptor Complex Is
    Required for Vacuolar Function in Arabidopsis.” <i>Cell Research</i>. Nature Publishing
    Group, 2011. <a href="https://doi.org/10.1038/cr.2011.99">https://doi.org/10.1038/cr.2011.99</a>.
  ieee: M. Zwiewka <i>et al.</i>, “The AP 3 adaptor complex is required for vacuolar
    function in Arabidopsis,” <i>Cell Research</i>, vol. 21, no. 12. Nature Publishing
    Group, pp. 1711–1722, 2011.
  ista: Zwiewka M, Feraru E, Möller B, Hwang I, Feraru M, Kleine Vehn J, Weijers D,
    Friml J. 2011. The AP 3 adaptor complex is required for vacuolar function in Arabidopsis.
    Cell Research. 21(12), 1711–1722.
  mla: Zwiewka, Marta, et al. “The AP 3 Adaptor Complex Is Required for Vacuolar Function
    in Arabidopsis.” <i>Cell Research</i>, vol. 21, no. 12, Nature Publishing Group,
    2011, pp. 1711–22, doi:<a href="https://doi.org/10.1038/cr.2011.99">10.1038/cr.2011.99</a>.
  short: M. Zwiewka, E. Feraru, B. Möller, I. Hwang, M. Feraru, J. Kleine Vehn, D.
    Weijers, J. Friml, Cell Research 21 (2011) 1711–1722.
date_created: 2018-12-11T12:01:23Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2021-01-12T07:41:04Z
day: '01'
doi: 10.1038/cr.2011.99
extern: 1
intvolume: '        21'
issue: '12'
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357998/
month: '01'
oa: 1
page: 1711 - 1722
publication: Cell Research
publication_status: published
publisher: Nature Publishing Group
publist_id: '3597'
quality_controlled: 0
status: public
title: The AP 3 adaptor complex is required for vacuolar function in Arabidopsis
type: journal_article
volume: 21
year: '2011'
...
---
_id: '3102'
abstract:
- lang: eng
  text: 'Multicellular organisms depend on cell production, cell fate specification,
    and correct patterning to shape their adult body. In plants, auxin plays a prominent
    role in the timely coordination of these different cellular processes. A well-studied
    example is lateral root initiation, in which auxin triggers founder cell specification
    and cell cycle activation of xylem pole–positioned pericycle cells. Here, we report
    that the E2Fa transcription factor of Arabidopsis thaliana is an essential component
    that regulates the asymmetric cell division marking lateral root initiation. Moreover,
    we demonstrate that E2Fa expression is regulated by the LATERAL ORGAN BOUNDARY
    DOMAIN18/LATERAL ORGAN BOUNDARY DOMAIN33 (LBD18/LBD33) dimer that is, in turn,
    regulated by the auxin signaling pathway. LBD18/LBD33 mediates lateral root organogenesis
    through E2Fa transcriptional activation, whereas E2Fa expression under control
    of the LBD18 promoter eliminates the need for LBD18. Besides lateral root initiation,
    vascular patterning is disrupted in E2Fa knockout plants, similarly as it is affected
    in auxin signaling and lbd mutants, indicating that the transcriptional induction
    of E2Fa through LBDs represents a general mechanism for auxin-dependent cell cycle
    activation. Our data illustrate how a conserved mechanism driving cell cycle entry
    has been adapted evolutionarily to connect auxin signaling with control of processes
    determining plant architecture. '
author:
- first_name: Barbara
  full_name: Berckmans, Barbara
  last_name: Berckmans
- first_name: Valya
  full_name: Vassileva, Valya
  last_name: Vassileva
- first_name: Stephan
  full_name: Schmid, Stephan P
  last_name: Schmid
- first_name: Sara
  full_name: Maes, Sara
  last_name: Maes
- first_name: Boris
  full_name: Parizot, Boris
  last_name: Parizot
- first_name: Satoshi
  full_name: Naramoto, Satoshi
  last_name: Naramoto
- first_name: Zoltan
  full_name: Magyar, Zoltan
  last_name: Magyar
- first_name: Claire
  full_name: Lessa Alvim Kamei, Claire
  last_name: Lessa Alvim Kamei
- first_name: Csaba
  full_name: Koncz, Csaba
  last_name: Koncz
- first_name: Laszlo
  full_name: Bögre, Laszlo
  last_name: Bögre
- first_name: Geert
  full_name: Persiau, Geert
  last_name: Persiau
- first_name: Geert
  full_name: De Jaeger, Geert
  last_name: De Jaeger
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Rüdiger
  full_name: Simon, Rüdiger
  last_name: Simon
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Lieven
  full_name: de Veyldera, Lieven
  last_name: De Veyldera
citation:
  ama: Berckmans B, Vassileva V, Schmid S, et al. Auxin Dependent cell cycle reactivation
    through transcriptional regulation of arabidopsis E2Fa by lateral organ boundary
    proteins. <i>Plant Cell</i>. 2011;23(10):3671-3683. doi:<a href="https://doi.org/10.1105/tpc.111.088377">10.1105/tpc.111.088377</a>
  apa: Berckmans, B., Vassileva, V., Schmid, S., Maes, S., Parizot, B., Naramoto,
    S., … De Veyldera, L. (2011). Auxin Dependent cell cycle reactivation through
    transcriptional regulation of arabidopsis E2Fa by lateral organ boundary proteins.
    <i>Plant Cell</i>. American Society of Plant Biologists. <a href="https://doi.org/10.1105/tpc.111.088377">https://doi.org/10.1105/tpc.111.088377</a>
  chicago: Berckmans, Barbara, Valya Vassileva, Stephan Schmid, Sara Maes, Boris Parizot,
    Satoshi Naramoto, Zoltan Magyar, et al. “Auxin Dependent Cell Cycle Reactivation
    through Transcriptional Regulation of Arabidopsis E2Fa by Lateral Organ Boundary
    Proteins.” <i>Plant Cell</i>. American Society of Plant Biologists, 2011. <a href="https://doi.org/10.1105/tpc.111.088377">https://doi.org/10.1105/tpc.111.088377</a>.
  ieee: B. Berckmans <i>et al.</i>, “Auxin Dependent cell cycle reactivation through
    transcriptional regulation of arabidopsis E2Fa by lateral organ boundary proteins,”
    <i>Plant Cell</i>, vol. 23, no. 10. American Society of Plant Biologists, pp.
    3671–3683, 2011.
  ista: Berckmans B, Vassileva V, Schmid S, Maes S, Parizot B, Naramoto S, Magyar
    Z, Lessa Alvim Kamei C, Koncz C, Bögre L, Persiau G, De Jaeger G, Friml J, Simon
    R, Beeckman T, De Veyldera L. 2011. Auxin Dependent cell cycle reactivation through
    transcriptional regulation of arabidopsis E2Fa by lateral organ boundary proteins.
    Plant Cell. 23(10), 3671–3683.
  mla: Berckmans, Barbara, et al. “Auxin Dependent Cell Cycle Reactivation through
    Transcriptional Regulation of Arabidopsis E2Fa by Lateral Organ Boundary Proteins.”
    <i>Plant Cell</i>, vol. 23, no. 10, American Society of Plant Biologists, 2011,
    pp. 3671–83, doi:<a href="https://doi.org/10.1105/tpc.111.088377">10.1105/tpc.111.088377</a>.
  short: B. Berckmans, V. Vassileva, S. Schmid, S. Maes, B. Parizot, S. Naramoto,
    Z. Magyar, C. Lessa Alvim Kamei, C. Koncz, L. Bögre, G. Persiau, G. De Jaeger,
    J. Friml, R. Simon, T. Beeckman, L. De Veyldera, Plant Cell 23 (2011) 3671–3683.
date_created: 2018-12-11T12:01:24Z
date_published: 2011-10-14T00:00:00Z
date_updated: 2021-01-12T07:41:04Z
day: '14'
doi: 10.1105/tpc.111.088377
extern: 1
intvolume: '        23'
issue: '10'
month: '10'
page: 3671 - 3683
publication: Plant Cell
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '3598'
quality_controlled: 0
status: public
title: Auxin Dependent cell cycle reactivation through transcriptional regulation
  of arabidopsis E2Fa by lateral organ boundary proteins
type: journal_article
volume: 23
year: '2011'
...
---
_id: '3103'
abstract:
- lang: eng
  text: Endocytosis in plants has an essential role not only for basic cellular functions
    but also for growth and development, hormonal signaling and communication with
    the environment including nutrient delivery, toxin avoidance, and pathogen defense.
    The major endocytic mechanism in plants depends on the coat protein clathrin.
    It starts by clathrin-coated vesicle formation at the plasma membrane, where specific
    cargoes are recognized and packaged for internalization. Recently, genetic, biochemical
    and advanced microscopy studies provided initial insights into mechanisms and
    roles of clathrin-mediated endocytosis in plants. Here we summarize the present
    state of knowledge and compare mechanisms of clathrin-mediated endocytosis in
    plants with animal and yeast paradigms as well as review plant-specific regulations
    and roles of this process.
author:
- first_name: Xu
  full_name: Chen, Xu
  id: 4E5ADCAA-F248-11E8-B48F-1D18A9856A87
  last_name: Chen
- first_name: Niloufer
  full_name: Irani, Niloufer
  last_name: Irani
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: 'Chen X, Irani N, Friml J. Clathrin-mediated endocytosis: The gateway into
    plant cells. <i>Current Opinion in Plant Biology</i>. 2011;14(6):674-682. doi:<a
    href="https://doi.org/10.1016/j.pbi.2011.08.006">10.1016/j.pbi.2011.08.006</a>'
  apa: 'Chen, X., Irani, N., &#38; Friml, J. (2011). Clathrin-mediated endocytosis:
    The gateway into plant cells. <i>Current Opinion in Plant Biology</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.pbi.2011.08.006">https://doi.org/10.1016/j.pbi.2011.08.006</a>'
  chicago: 'Chen, Xu, Niloufer Irani, and Jiří Friml. “Clathrin-Mediated Endocytosis:
    The Gateway into Plant Cells.” <i>Current Opinion in Plant Biology</i>. Elsevier,
    2011. <a href="https://doi.org/10.1016/j.pbi.2011.08.006">https://doi.org/10.1016/j.pbi.2011.08.006</a>.'
  ieee: 'X. Chen, N. Irani, and J. Friml, “Clathrin-mediated endocytosis: The gateway
    into plant cells,” <i>Current Opinion in Plant Biology</i>, vol. 14, no. 6. Elsevier,
    pp. 674–682, 2011.'
  ista: 'Chen X, Irani N, Friml J. 2011. Clathrin-mediated endocytosis: The gateway
    into plant cells. Current Opinion in Plant Biology. 14(6), 674–682.'
  mla: 'Chen, Xu, et al. “Clathrin-Mediated Endocytosis: The Gateway into Plant Cells.”
    <i>Current Opinion in Plant Biology</i>, vol. 14, no. 6, Elsevier, 2011, pp. 674–82,
    doi:<a href="https://doi.org/10.1016/j.pbi.2011.08.006">10.1016/j.pbi.2011.08.006</a>.'
  short: X. Chen, N. Irani, J. Friml, Current Opinion in Plant Biology 14 (2011) 674–682.
date_created: 2018-12-11T12:01:24Z
date_published: 2011-12-01T00:00:00Z
date_updated: 2021-01-12T07:41:05Z
day: '01'
doi: 10.1016/j.pbi.2011.08.006
extern: '1'
intvolume: '        14'
issue: '6'
language:
- iso: eng
month: '12'
oa_version: None
page: 674 - 682
publication: Current Opinion in Plant Biology
publication_status: published
publisher: Elsevier
publist_id: '3596'
quality_controlled: '1'
status: public
title: 'Clathrin-mediated endocytosis: The gateway into plant cells'
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 14
year: '2011'
...
