---
_id: '10116'
abstract:
- lang: eng
text: The ubiquitous Ca2+ sensor calmodulin (CaM) binds and regulates many proteins,
including ion channels, CaM kinases, and calcineurin, according to Ca2+-CaM levels.
What regulates neuronal CaM levels, is, however, unclear. CaM-binding transcription
activators (CAMTAs) are ancient proteins expressed broadly in nervous systems
and whose loss confers pleiotropic behavioral defects in flies, mice, and humans.
Using Caenorhabditis elegans and Drosophila, we show that CAMTAs control neuronal
CaM levels. The behavioral and neuronal Ca2+ signaling defects in mutants lacking
camt-1, the sole C. elegans CAMTA, can be rescued by supplementing neuronal CaM.
CAMT-1 binds multiple sites in the CaM promoter and deleting these sites phenocopies
camt-1. Our data suggest CAMTAs mediate a conserved and general mechanism that
controls neuronal CaM levels, thereby regulating Ca2+ signaling, physiology, and
behavior.
acknowledgement: The authors thank the MRC-LMB Flow Cytometry facility and Imaging
Service for support, the Cancer Research UK Cambridge Institute Genomics Core for
Next Generation Sequencing, Julie Ahringer and Alex Appert for advice and technical
help for ChIP-seq experiments, Paula Freire-Pritchett, Tim Stevens, and Gurpreet
Ghattaoraya for RNA-seq and ChIP-seq analyses, Nikos Chronis for the TN-XL plasmid,
Hong-Sheng Li and Daisuke Yamamoto for generously sending the tes2 and cro mutants,
Daria Siekhaus for hosting the fly work, Michaela Misova for technical assistance.
The authors are very grateful to Salihah Ece Sönmez for teaching us how to dissect,
mount and stain Drosophila retinae. This work was supported by an Advanced ERC grant
(269058 ACMO) and a Wellcome Investigator Award (209504/Z/17/Z) to MdB, and an IST
Plus Fellowship to TV-B (Marie Sklodowska-Curie Agreement no 754411).
article_number: e68238
article_processing_charge: No
article_type: original
author:
- first_name: Thanh
full_name: Vuong-Brender, Thanh
id: D389312E-10C4-11EA-ABF4-A4B43DDC885E
last_name: Vuong-Brender
- first_name: Sean
full_name: Flynn, Sean
last_name: Flynn
- first_name: Yvonne
full_name: Vallis, Yvonne
id: 05A2795C-31B5-11EA-83A7-7DA23DDC885E
last_name: Vallis
- first_name: Mario
full_name: De Bono, Mario
id: 4E3FF80E-F248-11E8-B48F-1D18A9856A87
last_name: De Bono
orcid: 0000-0001-8347-0443
citation:
ama: Vuong-Brender T, Flynn S, Vallis Y, de Bono M. Neuronal calmodulin levels are
controlled by CAMTA transcription factors. eLife. 2021;10. doi:10.7554/eLife.68238
apa: Vuong-Brender, T., Flynn, S., Vallis, Y., & de Bono, M. (2021). Neuronal
calmodulin levels are controlled by CAMTA transcription factors. ELife.
eLife Sciences Publications. https://doi.org/10.7554/eLife.68238
chicago: Vuong-Brender, Thanh, Sean Flynn, Yvonne Vallis, and Mario de Bono. “Neuronal
Calmodulin Levels Are Controlled by CAMTA Transcription Factors.” ELife.
eLife Sciences Publications, 2021. https://doi.org/10.7554/eLife.68238.
ieee: T. Vuong-Brender, S. Flynn, Y. Vallis, and M. de Bono, “Neuronal calmodulin
levels are controlled by CAMTA transcription factors,” eLife, vol. 10.
eLife Sciences Publications, 2021.
ista: Vuong-Brender T, Flynn S, Vallis Y, de Bono M. 2021. Neuronal calmodulin levels
are controlled by CAMTA transcription factors. eLife. 10, e68238.
mla: Vuong-Brender, Thanh, et al. “Neuronal Calmodulin Levels Are Controlled by
CAMTA Transcription Factors.” ELife, vol. 10, e68238, eLife Sciences Publications,
2021, doi:10.7554/eLife.68238.
short: T. Vuong-Brender, S. Flynn, Y. Vallis, M. de Bono, ELife 10 (2021).
date_created: 2021-10-10T22:01:22Z
date_published: 2021-09-17T00:00:00Z
date_updated: 2023-08-14T07:23:39Z
day: '17'
ddc:
- '610'
department:
- _id: MaDe
doi: 10.7554/eLife.68238
ec_funded: 1
external_id:
isi:
- '000695716100001'
pmid:
- '34499028'
file:
- access_level: open_access
checksum: b465e172d2b1f57aa26a2571a085d052
content_type: application/pdf
creator: cchlebak
date_created: 2021-10-11T14:15:07Z
date_updated: 2021-10-11T14:15:07Z
file_id: '10122'
file_name: 2021_eLife_VuongBrender.pdf
file_size: 1774624
relation: main_file
success: 1
file_date_updated: 2021-10-11T14:15:07Z
has_accepted_license: '1'
intvolume: ' 10'
isi: 1
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: eLife
publication_identifier:
eissn:
- 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: Neuronal calmodulin levels are controlled by CAMTA transcription factors
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: 10
year: '2021'
...
---
_id: '10117'
abstract:
- lang: eng
text: Proximity labeling provides a powerful in vivo tool to characterize the proteome
of subcellular structures and the interactome of specific proteins. The nematode
Caenorhabditis elegans is one of the most intensely studied organisms in biology,
offering many advantages for biochemistry. Using the highly active biotin ligase
TurboID, we optimize here a proximity labeling protocol for C. elegans. An advantage
of TurboID is that biotin's high affinity for streptavidin means biotin-labeled
proteins can be affinity-purified under harsh denaturing conditions. By combining
extensive sonication with aggressive denaturation using SDS and urea, we achieved
near-complete solubilization of worm proteins. We then used this protocol to characterize
the proteomes of the worm gut, muscle, skin, and nervous system. Neurons are among
the smallest C. elegans cells. To probe the method's sensitivity, we expressed
TurboID exclusively in the two AFD neurons and showed that the protocol could
identify known and previously unknown proteins expressed selectively in AFD. The
active zones of synapses are composed of a protein matrix that is difficult to
solubilize and purify. To test if our protocol could solubilize active zone proteins,
we knocked TurboID into the endogenous elks-1 gene, which encodes a presynaptic
active zone protein. We identified many known ELKS-1-interacting active zone proteins,
as well as previously uncharacterized synaptic proteins. Versatile vectors and
the inherent advantages of using C. elegans, including fast growth and the ability
to rapidly make and functionally test knock-ins, make proximity labeling a valuable
addition to the armory of this model organism.
acknowledgement: We thank de Bono lab members for helpful comments on the manuscript,
IST Austria and University of Vienna Mass Spec Facilities for invaluable discussions
and comments for the optimization of mass spec analyses of worm samples. The biotin
auxotropic E. coli strain MG1655bioB:kan was gift from John Cronan (University of
Illinois) and was kindly sent to us by Jessica Feldman and Ariana Sanchez (Stanford
University). dg398 pEntryslot2_mNeongreen::3XFLAG::stop and dg397 pEntryslot3_mNeongreen::3XFLAG::stop::unc-54
3′UTR entry vector were kindly shared by Dr Dominique Glauser (University of Fribourg).
Codon-optimized mScarlet vector was a generous gift from Dr Manuel Zimmer (University
of Vienna).
article_number: '101094'
article_processing_charge: Yes
article_type: original
author:
- first_name: Murat
full_name: Artan, Murat
id: C407B586-6052-11E9-B3AE-7006E6697425
last_name: Artan
orcid: 0000-0001-8945-6992
- first_name: Stephen
full_name: Barratt, Stephen
id: 57740d2b-2a88-11ec-97cf-d9e6d1b39677
last_name: Barratt
- first_name: Sean M.
full_name: Flynn, Sean M.
last_name: Flynn
- first_name: Farida
full_name: Begum, Farida
last_name: Begum
- first_name: Mark
full_name: Skehel, Mark
last_name: Skehel
- first_name: Armel
full_name: Nicolas, Armel
id: 2A103192-F248-11E8-B48F-1D18A9856A87
last_name: Nicolas
- first_name: Mario
full_name: De Bono, Mario
id: 4E3FF80E-F248-11E8-B48F-1D18A9856A87
last_name: De Bono
orcid: 0000-0001-8347-0443
citation:
ama: Artan M, Barratt S, Flynn SM, et al. Interactome analysis of Caenorhabditis
elegans synapses by TurboID-based proximity labeling. Journal of Biological
Chemistry. 2021;297(3). doi:10.1016/J.JBC.2021.101094
apa: Artan, M., Barratt, S., Flynn, S. M., Begum, F., Skehel, M., Nicolas, A., &
de Bono, M. (2021). Interactome analysis of Caenorhabditis elegans synapses by
TurboID-based proximity labeling. Journal of Biological Chemistry. Elsevier.
https://doi.org/10.1016/J.JBC.2021.101094
chicago: Artan, Murat, Stephen Barratt, Sean M. Flynn, Farida Begum, Mark Skehel,
Armel Nicolas, and Mario de Bono. “Interactome Analysis of Caenorhabditis Elegans
Synapses by TurboID-Based Proximity Labeling.” Journal of Biological Chemistry.
Elsevier, 2021. https://doi.org/10.1016/J.JBC.2021.101094.
ieee: M. Artan et al., “Interactome analysis of Caenorhabditis elegans synapses
by TurboID-based proximity labeling,” Journal of Biological Chemistry,
vol. 297, no. 3. Elsevier, 2021.
ista: Artan M, Barratt S, Flynn SM, Begum F, Skehel M, Nicolas A, de Bono M. 2021.
Interactome analysis of Caenorhabditis elegans synapses by TurboID-based proximity
labeling. Journal of Biological Chemistry. 297(3), 101094.
mla: Artan, Murat, et al. “Interactome Analysis of Caenorhabditis Elegans Synapses
by TurboID-Based Proximity Labeling.” Journal of Biological Chemistry,
vol. 297, no. 3, 101094, Elsevier, 2021, doi:10.1016/J.JBC.2021.101094.
short: M. Artan, S. Barratt, S.M. Flynn, F. Begum, M. Skehel, A. Nicolas, M. de
Bono, Journal of Biological Chemistry 297 (2021).
date_created: 2021-10-10T22:01:23Z
date_published: 2021-09-01T00:00:00Z
date_updated: 2023-08-14T07:24:09Z
day: '01'
ddc:
- '612'
department:
- _id: MaDe
- _id: LifeSc
doi: 10.1016/J.JBC.2021.101094
ec_funded: 1
external_id:
isi:
- '000706409200006'
file:
- access_level: open_access
checksum: 19e39d36c5b9387c6dc0e89c9ae856ab
content_type: application/pdf
creator: cchlebak
date_created: 2021-10-11T12:20:58Z
date_updated: 2021-10-11T12:20:58Z
file_id: '10121'
file_name: 2021_JBC_Artan.pdf
file_size: 1680010
relation: main_file
success: 1
file_date_updated: 2021-10-11T12:20:58Z
has_accepted_license: '1'
intvolume: ' 297'
isi: 1
issue: '3'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: Journal of Biological Chemistry
publication_identifier:
eissn:
- 1083-351X
issn:
- 0021-9258
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Interactome analysis of Caenorhabditis elegans synapses by TurboID-based proximity
labeling
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: 297
year: '2021'
...
---
_id: '10123'
abstract:
- lang: eng
text: Solution synthesis of particles emerged as an alternative to prepare thermoelectric
materials with less demanding processing conditions than conventional solid-state
synthetic methods. However, solution synthesis generally involves the presence
of additional molecules or ions belonging to the precursors or added to enable
solubility and/or regulate nucleation and growth. These molecules or ions can
end up in the particles as surface adsorbates and interfere in the material properties.
This work demonstrates that ionic adsorbates, in particular Na⁺ ions, are electrostatically
adsorbed in SnSe particles synthesized in water and play a crucial role not only
in directing the material nano/microstructure but also in determining the transport
properties of the consolidated material. In dense pellets prepared by sintering
SnSe particles, Na remains within the crystal lattice as dopant, in dislocations,
precipitates, and forming grain boundary complexions. These results highlight
the importance of considering all the possible unintentional impurities to establish
proper structure-property relationships and control material properties in solution-processed
thermoelectric materials.
acknowledged_ssus:
- _id: EM-Fac
- _id: NanoFab
acknowledgement: 'Y.L. and M.C. contributed equally to this work. This research was
supported by the Scientific Service Units (SSU) of IST Austria through resources
provided by Electron Microscopy Facility (EMF) and the Nanofabrication Facility
(NNF). This work was financially supported by IST Austria and the Werner Siemens
Foundation. Y.L. acknowledges funding from the European Union''s Horizon 2020 research
and innovation program under the Marie Sklodowska-Curie grant agreement No. 754411.
M.C. has received funding from the European Union''s Horizon 2020 research and innovation
program under the Marie Skłodowska-Curie Grant Agreement No. 665385. Y.Y. and O.C.-M.
acknowledge the financial support from DFG within the project SFB 917: Nanoswitches.
J.L. is a Serra Húnter Fellow and is grateful to ICREA Academia program. C.C. acknowledges
funding from the FWF “Lise Meitner Fellowship” grant agreement M 2889-N.'
article_number: '2106858'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Yu
full_name: Liu, Yu
id: 2A70014E-F248-11E8-B48F-1D18A9856A87
last_name: Liu
orcid: 0000-0001-7313-6740
- first_name: Mariano
full_name: Calcabrini, Mariano
id: 45D7531A-F248-11E8-B48F-1D18A9856A87
last_name: Calcabrini
orcid: 0000-0003-4566-5877
- first_name: Yuan
full_name: Yu, Yuan
last_name: Yu
- first_name: Aziz
full_name: Genç, Aziz
last_name: Genç
- first_name: Cheng
full_name: Chang, Cheng
id: 9E331C2E-9F27-11E9-AE48-5033E6697425
last_name: Chang
orcid: 0000-0002-9515-4277
- first_name: Tommaso
full_name: Costanzo, Tommaso
id: D93824F4-D9BA-11E9-BB12-F207E6697425
last_name: Costanzo
orcid: 0000-0001-9732-3815
- first_name: Tobias
full_name: Kleinhanns, Tobias
id: 8BD9DE16-AB3C-11E9-9C8C-2A03E6697425
last_name: Kleinhanns
- first_name: Seungho
full_name: Lee, Seungho
id: BB243B88-D767-11E9-B658-BC13E6697425
last_name: Lee
orcid: 0000-0002-6962-8598
- first_name: Jordi
full_name: Llorca, Jordi
last_name: Llorca
- first_name: Oana
full_name: Cojocaru‐Mirédin, Oana
last_name: Cojocaru‐Mirédin
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
citation:
ama: 'Liu Y, Calcabrini M, Yu Y, et al. The importance of surface adsorbates in
solution‐processed thermoelectric materials: The case of SnSe. Advanced Materials.
2021;33(52). doi:10.1002/adma.202106858'
apa: 'Liu, Y., Calcabrini, M., Yu, Y., Genç, A., Chang, C., Costanzo, T., … Ibáñez,
M. (2021). The importance of surface adsorbates in solution‐processed thermoelectric
materials: The case of SnSe. Advanced Materials. Wiley. https://doi.org/10.1002/adma.202106858'
chicago: 'Liu, Yu, Mariano Calcabrini, Yuan Yu, Aziz Genç, Cheng Chang, Tommaso
Costanzo, Tobias Kleinhanns, et al. “The Importance of Surface Adsorbates in Solution‐processed
Thermoelectric Materials: The Case of SnSe.” Advanced Materials. Wiley,
2021. https://doi.org/10.1002/adma.202106858.'
ieee: 'Y. Liu et al., “The importance of surface adsorbates in solution‐processed
thermoelectric materials: The case of SnSe,” Advanced Materials, vol. 33,
no. 52. Wiley, 2021.'
ista: 'Liu Y, Calcabrini M, Yu Y, Genç A, Chang C, Costanzo T, Kleinhanns T, Lee
S, Llorca J, Cojocaru‐Mirédin O, Ibáñez M. 2021. The importance of surface adsorbates
in solution‐processed thermoelectric materials: The case of SnSe. Advanced Materials.
33(52), 2106858.'
mla: 'Liu, Yu, et al. “The Importance of Surface Adsorbates in Solution‐processed
Thermoelectric Materials: The Case of SnSe.” Advanced Materials, vol. 33,
no. 52, 2106858, Wiley, 2021, doi:10.1002/adma.202106858.'
short: Y. Liu, M. Calcabrini, Y. Yu, A. Genç, C. Chang, T. Costanzo, T. Kleinhanns,
S. Lee, J. Llorca, O. Cojocaru‐Mirédin, M. Ibáñez, Advanced Materials 33 (2021).
date_created: 2021-10-11T20:07:24Z
date_published: 2021-12-29T00:00:00Z
date_updated: 2023-08-14T07:25:27Z
day: '29'
ddc:
- '620'
department:
- _id: EM-Fac
- _id: MaIb
doi: 10.1002/adma.202106858
ec_funded: 1
external_id:
isi:
- '000709899300001'
pmid:
- '34626034'
file:
- access_level: open_access
checksum: 990bccc527c64d85cf1c97885110b5f4
content_type: application/pdf
creator: cchlebak
date_created: 2022-02-03T13:16:14Z
date_updated: 2022-02-03T13:16:14Z
file_id: '10720'
file_name: 2021_AdvancedMaterials_Liu.pdf
file_size: 5595666
relation: main_file
success: 1
file_date_updated: 2022-02-03T13:16:14Z
has_accepted_license: '1'
intvolume: ' 33'
isi: 1
issue: '52'
keyword:
- mechanical engineering
- mechanics of materials
- general materials science
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
- _id: 9B8804FC-BA93-11EA-9121-9846C619BF3A
grant_number: M02889
name: Bottom-up Engineering for Thermoelectric Applications
- _id: 9B8F7476-BA93-11EA-9121-9846C619BF3A
name: 'HighTE: The Werner Siemens Laboratory for the High Throughput Discovery of
Semiconductors for Waste Heat Recovery'
publication: Advanced Materials
publication_identifier:
eissn:
- 1521-4095
issn:
- 0935-9648
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
record:
- id: '12885'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: 'The importance of surface adsorbates in solution‐processed thermoelectric
materials: The case of SnSe'
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: 33
year: '2021'
...
---
_id: '10124'
abstract:
- lang: eng
text: The transport of macromolecules and nanoscopic particles to a target cellular
site is a crucial aspect in many physiological processes. This directional motion
is generally controlled via active mechanical and chemical processes. Here we
show, by means of molecular dynamics simulations and an analytical theory, that
completely passive nanoparticles can exhibit directional motion when embedded
in non-uniform mechanical environments. Specifically, we study the motion of a
passive nanoparticle adhering to a mechanically non-uniform elastic membrane.
We observe a non-monotonic affinity of the particle to the membrane as a function
of the membrane’s rigidity, which results in the particle transport. This transport
can be both up or down the rigidity gradient, depending on the absolute values
of the rigidities that the gradient spans across. We conclude that rigidity gradients
can be used to direct average motion of passive macromolecules and nanoparticles
on deformable membranes, resulting in the preferential accumulation of the macromolecules
in regions of certain mechanical properties.
acknowledgement: We acknowledge support from the Engineering and Physical Sciences
Research Council (A.P. and A.Š.), the Royal Society (A.Š.) and the European Research
Council (I.P. and A.Š.).
article_processing_charge: No
article_type: original
author:
- first_name: Ivan
full_name: Palaia, Ivan
last_name: Palaia
- first_name: Alexandru
full_name: Paraschiv, Alexandru
last_name: Paraschiv
- first_name: Vincent
full_name: Debets, Vincent
last_name: Debets
- first_name: Cornelis
full_name: Storm, Cornelis
last_name: Storm
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
citation:
ama: Palaia I, Paraschiv A, Debets V, Storm C, Šarić A. Durotaxis of passive nanoparticles
on elastic membranes. ACS Nano. 2021. doi:10.1021/acsnano.1c02777
apa: Palaia, I., Paraschiv, A., Debets, V., Storm, C., & Šarić, A. (2021). Durotaxis
of passive nanoparticles on elastic membranes. ACS Nano. American Chemical
Society. https://doi.org/10.1021/acsnano.1c02777
chicago: Palaia, Ivan, Alexandru Paraschiv, Vincent Debets, Cornelis Storm, and
Anđela Šarić. “Durotaxis of Passive Nanoparticles on Elastic Membranes.” ACS
Nano. American Chemical Society, 2021. https://doi.org/10.1021/acsnano.1c02777 .
ieee: I. Palaia, A. Paraschiv, V. Debets, C. Storm, and A. Šarić, “Durotaxis of
passive nanoparticles on elastic membranes,” ACS Nano. American Chemical
Society, 2021.
ista: Palaia I, Paraschiv A, Debets V, Storm C, Šarić A. 2021. Durotaxis of passive
nanoparticles on elastic membranes. ACS Nano.
mla: Palaia, Ivan, et al. “Durotaxis of Passive Nanoparticles on Elastic Membranes.”
ACS Nano, American Chemical Society, 2021, doi:10.1021/acsnano.1c02777 .
short: I. Palaia, A. Paraschiv, V. Debets, C. Storm, A. Šarić, ACS Nano (2021).
date_created: 2021-10-12T07:31:21Z
date_published: 2021-09-22T00:00:00Z
date_updated: 2021-10-12T09:50:19Z
day: '22'
doi: '10.1021/acsnano.1c02777 '
extern: '1'
external_id:
pmid:
- '34550677 '
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.biorxiv.org/content/10.1101/2021.04.01.438065
month: '09'
oa: 1
oa_version: Preprint
pmid: 1
publication: ACS Nano
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
status: public
title: Durotaxis of passive nanoparticles on elastic membranes
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2021'
...
---
_id: '10125'
abstract:
- lang: eng
text: Living systems propagate by undergoing rounds of cell growth and division.
Cell division is at heart a physical process that requires mechanical forces,
usually exerted by protein assemblies. Here we developed the first physical model
for the division of archaeal cells, which despite their structural simplicity
share machinery and evolutionary origins with eukaryotes. We show how active geometry
changes of elastic ESCRT-III filaments, coupled to filament disassembly, are sufficient
to efficiently split the cell. We explore how the non-equilibrium processes that
govern the filament behaviour impact the resulting cell division. We show how
a quantitative comparison between our simulations and dynamic data for ESCRTIII-mediated
division in Sulfolobus acidocaldarius, the closest archaeal relative to eukaryotic
cells that can currently be cultured in the lab, and reveal the most likely physical
mechanism behind its division.
acknowledgement: We acknowledge support from the Biotechnology and Biological Sciences
Research Council (L.H.K.), EPSRC (A.E.H), UCL IPLS (T.Y and D. H.), Wellcome Trust
(203276/Z/16/Z, A.P., S.C., R. H., B.B.), Volkswagen Foundation (Az 96727, A.P.,
B.B., A.Š.), MRC (MC CF1226, R.H., B.B., A.Š.), the ERC grant (”NEPA” 802960, A.Š.),
the Royal Society (C.V.-H., A.Š.), the UK Materials and Molecular Modelling Hub
for computational resources (EP/P020194/1).
article_processing_charge: No
author:
- first_name: L.
full_name: Harker-Kirschneck, L.
last_name: Harker-Kirschneck
- first_name: A. E.
full_name: Hafner, A. E.
last_name: Hafner
- first_name: T.
full_name: Yao, T.
last_name: Yao
- first_name: A.
full_name: Pulschen, A.
last_name: Pulschen
- first_name: F.
full_name: Hurtig, F.
last_name: Hurtig
- first_name: C.
full_name: Vanhille-Campos, C.
last_name: Vanhille-Campos
- first_name: D.
full_name: Hryniuk, D.
last_name: Hryniuk
- first_name: S.
full_name: Culley, S.
last_name: Culley
- first_name: R.
full_name: Henriques, R.
last_name: Henriques
- first_name: B.
full_name: Baum, B.
last_name: Baum
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
citation:
ama: Harker-Kirschneck L, Hafner AE, Yao T, et al. Physical mechanisms of ESCRT-III-driven
cell division in archaea. bioRxiv. doi:10.1101/2021.03.23.436559
apa: Harker-Kirschneck, L., Hafner, A. E., Yao, T., Pulschen, A., Hurtig, F., Vanhille-Campos,
C., … Šarić, A. (n.d.). Physical mechanisms of ESCRT-III-driven cell division
in archaea. bioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2021.03.23.436559
chicago: Harker-Kirschneck, L., A. E. Hafner, T. Yao, A. Pulschen, F. Hurtig, C.
Vanhille-Campos, D. Hryniuk, et al. “Physical Mechanisms of ESCRT-III-Driven Cell
Division in Archaea.” BioRxiv. Cold Spring Harbor Laboratory, n.d. https://doi.org/10.1101/2021.03.23.436559.
ieee: L. Harker-Kirschneck et al., “Physical mechanisms of ESCRT-III-driven
cell division in archaea,” bioRxiv. Cold Spring Harbor Laboratory.
ista: Harker-Kirschneck L, Hafner AE, Yao T, Pulschen A, Hurtig F, Vanhille-Campos
C, Hryniuk D, Culley S, Henriques R, Baum B, Šarić A. Physical mechanisms of ESCRT-III-driven
cell division in archaea. bioRxiv, 10.1101/2021.03.23.436559.
mla: Harker-Kirschneck, L., et al. “Physical Mechanisms of ESCRT-III-Driven Cell
Division in Archaea.” BioRxiv, Cold Spring Harbor Laboratory, doi:10.1101/2021.03.23.436559.
short: L. Harker-Kirschneck, A.E. Hafner, T. Yao, A. Pulschen, F. Hurtig, C. Vanhille-Campos,
D. Hryniuk, S. Culley, R. Henriques, B. Baum, A. Šarić, BioRxiv (n.d.).
date_created: 2021-10-12T07:45:07Z
date_published: 2021-03-23T00:00:00Z
date_updated: 2021-10-12T09:50:26Z
day: '23'
doi: 10.1101/2021.03.23.436559
extern: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.biorxiv.org/content/10.1101/2021.03.23.436559
month: '03'
oa: 1
oa_version: Preprint
publication: bioRxiv
publication_status: submitted
publisher: Cold Spring Harbor Laboratory
status: public
title: Physical mechanisms of ESCRT-III-driven cell division in archaea
type: preprint
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2021'
...
---
_id: '10134'
abstract:
- lang: eng
text: We investigate the effect of coupling between translational and internal degrees
of freedom of composite quantum particles on their localization in a random potential.
We show that entanglement between the two degrees of freedom weakens localization
due to the upper bound imposed on the inverse participation ratio by purity of
a quantum state. We perform numerical calculations for a two-particle system bound
by a harmonic force in a 1D disordered lattice and a rigid rotor in a 2D disordered
lattice. We illustrate that the coupling has a dramatic effect on localization
properties, even with a small number of internal states participating in quantum
dynamics.
acknowledgement: "We acknowledge helpful discussions with W. G. Unruh and A. Rodriguez.
F. S. is supported by European Union’s\r\nHorizon 2020 research and innovation programme
under the Marie Skłodowska-Curie Grant No. 754411. M. L. acknowledges support by
the European Research Council (ERC) Starting Grant No. 801770 (ANGULON). W. H. Z.
is\r\nsupported by Department of Energy under the Los\r\nAlamos National Laboratory
LDRD Program as well as by the U.S. Department of Energy, Office of Science, Basic\r\nEnergy
Sciences, Materials Sciences and Engineering Division, Condensed Matter Theory Program.
R. V. K. is supported by NSERC of Canada.\r\n"
article_number: '160602'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Fumika
full_name: Suzuki, Fumika
id: 650C99FC-1079-11EA-A3C0-73AE3DDC885E
last_name: Suzuki
orcid: 0000-0003-4982-5970
- first_name: Mikhail
full_name: Lemeshko, Mikhail
id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
last_name: Lemeshko
orcid: 0000-0002-6990-7802
- first_name: Wojciech H.
full_name: Zurek, Wojciech H.
last_name: Zurek
- first_name: Roman V.
full_name: Krems, Roman V.
last_name: Krems
citation:
ama: Suzuki F, Lemeshko M, Zurek WH, Krems RV. Anderson localization of composite
particles. Physical Review Letters. 2021;127(16). doi:10.1103/physrevlett.127.160602
apa: Suzuki, F., Lemeshko, M., Zurek, W. H., & Krems, R. V. (2021). Anderson
localization of composite particles. Physical Review Letters. American
Physical Society . https://doi.org/10.1103/physrevlett.127.160602
chicago: Suzuki, Fumika, Mikhail Lemeshko, Wojciech H. Zurek, and Roman V. Krems.
“Anderson Localization of Composite Particles.” Physical Review Letters.
American Physical Society , 2021. https://doi.org/10.1103/physrevlett.127.160602.
ieee: F. Suzuki, M. Lemeshko, W. H. Zurek, and R. V. Krems, “Anderson localization
of composite particles,” Physical Review Letters, vol. 127, no. 16. American
Physical Society , 2021.
ista: Suzuki F, Lemeshko M, Zurek WH, Krems RV. 2021. Anderson localization of composite
particles. Physical Review Letters. 127(16), 160602.
mla: Suzuki, Fumika, et al. “Anderson Localization of Composite Particles.” Physical
Review Letters, vol. 127, no. 16, 160602, American Physical Society , 2021,
doi:10.1103/physrevlett.127.160602.
short: F. Suzuki, M. Lemeshko, W.H. Zurek, R.V. Krems, Physical Review Letters 127
(2021).
date_created: 2021-10-13T09:21:33Z
date_published: 2021-10-12T00:00:00Z
date_updated: 2024-02-29T12:34:10Z
day: '12'
department:
- _id: MiLe
doi: 10.1103/physrevlett.127.160602
ec_funded: 1
external_id:
arxiv:
- '2011.06279'
isi:
- '000707495700001'
intvolume: ' 127'
isi: 1
issue: '16'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/2011.06279
month: '10'
oa: 1
oa_version: Preprint
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
- _id: 2688CF98-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '801770'
name: 'Angulon: physics and applications of a new quasiparticle'
publication: Physical Review Letters
publication_identifier:
eissn:
- 1079-7114
issn:
- 0031-9007
publication_status: published
publisher: 'American Physical Society '
quality_controlled: '1'
scopus_import: '1'
status: public
title: Anderson localization of composite particles
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 127
year: '2021'
...
---
_id: '10135'
abstract:
- lang: eng
text: "Plants maintain the capacity to develop new organs e.g. lateral roots post-embryonically
throughout their whole life and thereby flexibly adapt to ever-changing environmental
conditions. Plant hormones auxin and cytokinin are the main regulators of the
lateral root organogenesis. Additionally to their solo activities, the interaction
between auxin and\r\ncytokinin plays crucial role in fine-tuning of lateral root
development and growth. In particular, cytokinin modulates auxin distribution
within the developing lateral root by affecting the endomembrane trafficking of
auxin transporter PIN1 and promoting its vacuolar degradation (Marhavý et al.,
2011, 2014). This effect is independent of transcription and\r\ntranslation. Therefore,
it suggests novel, non-canonical cytokinin activity occuring possibly on the posttranslational
level. Impact of cytokinin and other plant hormones on auxin transporters (including
PIN1) on the posttranslational level is described in detail in the introduction
part of this thesis in a form of a review (Semeradova et al., 2020). To gain insights
into the molecular machinery underlying cytokinin effect on the endomembrane trafficking
in the plant cell, in particular on the PIN1 degradation, we conducted two large
proteomic screens: 1) Identification of cytokinin binding proteins using\r\nchemical
proteomics. 2) Monitoring of proteomic and phosphoproteomic changes upon cytokinin
treatment. In the first screen, we identified DYNAMIN RELATED PROTEIN 2A (DRP2A).
We found that DRP2A plays a role in cytokinin regulated processes during the plant
growth and that cytokinin treatment promotes destabilization of DRP2A protein.
However, the role of DRP2A in the PIN1 degradation remains to be elucidated. In
the second screen, we found VACUOLAR PROTEIN SORTING 9A (VPS9A). VPS9a plays crucial
role in plant’s response to cytokin and in cytokinin mediated PIN1 degradation.
Altogether, we identified proteins, which bind to cytokinin and proteins that
in response to\r\ncytokinin exhibit significantly changed abundance or phosphorylation
pattern. By combining information from these two screens, we can pave our way
towards understanding of noncanonical cytokinin effects."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Hana
full_name: Semerádová, Hana
id: 42FE702E-F248-11E8-B48F-1D18A9856A87
last_name: Semerádová
citation:
ama: Semerádová H. Molecular mechanisms of the cytokinin-regulated endomembrane
trafficking to coordinate plant organogenesis. 2021. doi:10.15479/at:ista:10135
apa: Semerádová, H. (2021). Molecular mechanisms of the cytokinin-regulated endomembrane
trafficking to coordinate plant organogenesis. Institute of Science and Technology
Austria. https://doi.org/10.15479/at:ista:10135
chicago: Semerádová, Hana. “Molecular Mechanisms of the Cytokinin-Regulated Endomembrane
Trafficking to Coordinate Plant Organogenesis.” Institute of Science and Technology
Austria, 2021. https://doi.org/10.15479/at:ista:10135.
ieee: H. Semerádová, “Molecular mechanisms of the cytokinin-regulated endomembrane
trafficking to coordinate plant organogenesis,” Institute of Science and Technology
Austria, 2021.
ista: Semerádová H. 2021. Molecular mechanisms of the cytokinin-regulated endomembrane
trafficking to coordinate plant organogenesis. Institute of Science and Technology
Austria.
mla: Semerádová, Hana. Molecular Mechanisms of the Cytokinin-Regulated Endomembrane
Trafficking to Coordinate Plant Organogenesis. Institute of Science and Technology
Austria, 2021, doi:10.15479/at:ista:10135.
short: H. Semerádová, Molecular Mechanisms of the Cytokinin-Regulated Endomembrane
Trafficking to Coordinate Plant Organogenesis, Institute of Science and Technology
Austria, 2021.
date_created: 2021-10-13T13:42:48Z
date_published: 2021-10-13T00:00:00Z
date_updated: 2024-01-25T10:53:29Z
day: '13'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: EvBe
doi: 10.15479/at:ista:10135
file:
- access_level: closed
checksum: ce7108853e6cec6224f17cd6429b51fe
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: cziletti
date_created: 2021-10-27T07:45:37Z
date_updated: 2022-12-20T23:30:05Z
embargo_to: open_access
file_id: '10186'
file_name: Hana_Semeradova_Disertation_Thesis_II_Revised_3.docx
file_size: 28508629
relation: source_file
- access_level: open_access
checksum: 0d7afb846e8e31ec794de47bf44e12ef
content_type: application/pdf
creator: cziletti
date_created: 2021-10-27T07:45:57Z
date_updated: 2022-12-20T23:30:05Z
embargo: 2022-10-28
file_id: '10187'
file_name: Hana_Semeradova_Disertation_Thesis_II_Revised_3PDFA.pdf
file_size: 10623525
relation: main_file
file_date_updated: 2022-12-20T23:30:05Z
has_accepted_license: '1'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
project:
- _id: 261821BC-B435-11E9-9278-68D0E5697425
grant_number: '24746'
name: Molecular mechanisms of the cytokinin regulated endomembrane trafficking to
coordinate plant organogenesis.
publication_identifier:
isbn:
- 978-3-99078-014-5
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '9160'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Eva
full_name: Benková, Eva
id: 38F4F166-F248-11E8-B48F-1D18A9856A87
last_name: Benková
orcid: 0000-0002-8510-9739
title: Molecular mechanisms of the cytokinin-regulated endomembrane trafficking to
coordinate plant organogenesis
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2021'
...
---
_id: '10144'
abstract:
- lang: eng
text: FGFs and their high-affinity receptors (FGFRs) play key roles in development,
tissue repair, and disease. Because FGFRs bind overlapping sets of ligands, their
individual functions cannot be determined using ligand stimulation. Here, we generated
a light-activated FGFR2 variant (OptoR2) to selectively activate signaling by
the major FGFR in keratinocytes. Illumination of OptoR2-expressing HEK 293T cells
activated FGFR signaling with remarkable temporal precision and promoted cell
migration and proliferation. In murine and human keratinocytes, OptoR2 activation
rapidly induced the classical FGFR signaling pathways and expression of FGF target
genes. Surprisingly, multi-level counter-regulation occurred in keratinocytes
in vitro and in transgenic mice in vivo, including OptoR2 down-regulation and
loss of responsiveness to light activation. These results demonstrate unexpected
cell type-specific limitations of optogenetic FGFRs in long-term in vitro and
in vivo settings and highlight the complex consequences of transferring optogenetic
cell signaling tools into their relevant cellular contexts.
acknowledgement: We thank Connor Richterich and Patricia Reinert, ETH Zurich, for
invaluable experimental help; Manuela Pérez Berlanga, University Zurich, for help
with the confocal imaging; Lukas Fischer for help with electrical engineering; Thomas
Hennek, Sol Taguinod, and Dr. Stephan Sonntag, EPIC Phenomics Center, ETH Zürich,
for the generation and maintenance of K14-OptoR2 mice; and Dr. Petra Boukamp, Leibniz
Institute, Düsseldorf, Germany, for early-passage HaCaT keratinocytes. This work
was supported by the ETH Zurich (grant ETH-06 15-1 to S Werner and L Maddaluno),
the Swiss National Science Foundation (grant 31003B-189364 to S Werner), and a Marie
Curie postdoctoral fellowship from the European Union (to L Maddaluno).
article_number: e202101100
article_processing_charge: Yes
article_type: original
author:
- first_name: Theresa
full_name: Rauschendorfer, Theresa
last_name: Rauschendorfer
- first_name: Selina
full_name: Gurri, Selina
last_name: Gurri
- first_name: Irina
full_name: Heggli, Irina
last_name: Heggli
- first_name: Luigi
full_name: Maddaluno, Luigi
last_name: Maddaluno
- first_name: Michael
full_name: Meyer, Michael
last_name: Meyer
- first_name: Álvaro
full_name: Inglés Prieto, Álvaro
id: 2A9DB292-F248-11E8-B48F-1D18A9856A87
last_name: Inglés Prieto
orcid: 0000-0002-5409-8571
- first_name: Harald L
full_name: Janovjak, Harald L
id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
last_name: Janovjak
orcid: 0000-0002-8023-9315
- first_name: Sabine
full_name: Werner, Sabine
last_name: Werner
citation:
ama: Rauschendorfer T, Gurri S, Heggli I, et al. Acute and chronic effects of a
light-activated FGF receptor in keratinocytes in vitro and in mice. Life Science
Alliance. 2021;4(11). doi:10.26508/lsa.202101100
apa: Rauschendorfer, T., Gurri, S., Heggli, I., Maddaluno, L., Meyer, M., Inglés
Prieto, Á., … Werner, S. (2021). Acute and chronic effects of a light-activated
FGF receptor in keratinocytes in vitro and in mice. Life Science Alliance.
Life Science Alliance. https://doi.org/10.26508/lsa.202101100
chicago: Rauschendorfer, Theresa, Selina Gurri, Irina Heggli, Luigi Maddaluno, Michael
Meyer, Álvaro Inglés Prieto, Harald L Janovjak, and Sabine Werner. “Acute and
Chronic Effects of a Light-Activated FGF Receptor in Keratinocytes in Vitro and
in Mice.” Life Science Alliance. Life Science Alliance, 2021. https://doi.org/10.26508/lsa.202101100.
ieee: T. Rauschendorfer et al., “Acute and chronic effects of a light-activated
FGF receptor in keratinocytes in vitro and in mice,” Life Science Alliance,
vol. 4, no. 11. Life Science Alliance, 2021.
ista: Rauschendorfer T, Gurri S, Heggli I, Maddaluno L, Meyer M, Inglés Prieto Á,
Janovjak HL, Werner S. 2021. Acute and chronic effects of a light-activated FGF
receptor in keratinocytes in vitro and in mice. Life Science Alliance. 4(11),
e202101100.
mla: Rauschendorfer, Theresa, et al. “Acute and Chronic Effects of a Light-Activated
FGF Receptor in Keratinocytes in Vitro and in Mice.” Life Science Alliance,
vol. 4, no. 11, e202101100, Life Science Alliance, 2021, doi:10.26508/lsa.202101100.
short: T. Rauschendorfer, S. Gurri, I. Heggli, L. Maddaluno, M. Meyer, Á. Inglés
Prieto, H.L. Janovjak, S. Werner, Life Science Alliance 4 (2021).
date_created: 2021-10-17T22:01:16Z
date_published: 2021-09-21T00:00:00Z
date_updated: 2022-08-31T14:01:56Z
day: '21'
ddc:
- '576'
doi: 10.26508/lsa.202101100
extern: '1'
external_id:
pmid:
- '34548382'
file:
- access_level: open_access
checksum: 89fb95b211dbe8678809e7cca4626952
content_type: application/pdf
creator: cchlebak
date_created: 2021-10-18T14:48:06Z
date_updated: 2021-10-18T14:48:06Z
file_id: '10152'
file_name: 2021_LifeScAlliance_Rauschendorfer.pdf
file_size: 2055981
relation: main_file
success: 1
file_date_updated: 2021-10-18T14:48:06Z
has_accepted_license: '1'
intvolume: ' 4'
issue: '11'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
publication: Life Science Alliance
publication_identifier:
eissn:
- 2575-1077
publication_status: published
publisher: Life Science Alliance
quality_controlled: '1'
scopus_import: '1'
status: public
title: Acute and chronic effects of a light-activated FGF receptor in keratinocytes
in vitro and in mice
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: 4
year: '2021'
...
---
_id: '10146'
abstract:
- lang: eng
text: The enzymes of the mitochondrial electron transport chain are key players
of cell metabolism. Despite being active when isolated, in vivo they associate
into supercomplexes1, whose precise role is debated. Supercomplexes CIII2CIV1-2
(refs. 2,3), CICIII2 (ref. 4) and CICIII2CIV (respirasome)5,6,7,8,9,10 exist in
mammals, but in contrast to CICIII2 and the respirasome, to date the only known
eukaryotic structures of CIII2CIV1-2 come from Saccharomyces cerevisiae11,12 and
plants13, which have different organization. Here we present the first, to our
knowledge, structures of mammalian (mouse and ovine) CIII2CIV and its assembly
intermediates, in different conformations. We describe the assembly of CIII2CIV
from the CIII2 precursor to the final CIII2CIV conformation, driven by the insertion
of the N terminus of the assembly factor SCAF1 (ref. 14) deep into CIII2, while
its C terminus is integrated into CIV. Our structures (which include CICIII2 and
the respirasome) also confirm that SCAF1 is exclusively required for the assembly
of CIII2CIV and has no role in the assembly of the respirasome. We show that CIII2
is asymmetric due to the presence of only one copy of subunit 9, which straddles
both monomers and prevents the attachment of a second copy of SCAF1 to CIII2,
explaining the presence of one copy of CIV in CIII2CIV in mammals. Finally, we
show that CIII2 and CIV gain catalytic advantage when assembled into the supercomplex
and propose a role for CIII2CIV in fine tuning the efficiency of electron transfer
in the electron transport chain.
acknowledged_ssus:
- _id: PreCl
- _id: EM-Fac
- _id: ScienComp
acknowledgement: We thank the pre-clinical facility of the IST Austria and A. Venturino
for assistance with the animals; and V.-V. Hodirnau for assistance during the Titan
Krios data collection, performed at the IST Austria. The data processing was performed
at the IST high-performance computing cluster. This project has received funding
from the European Union’s Horizon 2020 research and innovation program under the
Marie Skłodowska-Curie grant agreement no. 754411.
article_processing_charge: No
article_type: original
author:
- first_name: Irene
full_name: Vercellino, Irene
id: 3ED6AF16-F248-11E8-B48F-1D18A9856A87
last_name: Vercellino
orcid: 0000-0001-5618-3449
- first_name: Leonid A
full_name: Sazanov, Leonid A
id: 338D39FE-F248-11E8-B48F-1D18A9856A87
last_name: Sazanov
orcid: 0000-0002-0977-7989
citation:
ama: Vercellino I, Sazanov LA. Structure and assembly of the mammalian mitochondrial
supercomplex CIII2CIV. Nature. 2021;598(7880):364-367. doi:10.1038/s41586-021-03927-z
apa: Vercellino, I., & Sazanov, L. A. (2021). Structure and assembly of the
mammalian mitochondrial supercomplex CIII2CIV. Nature. Springer
Nature. https://doi.org/10.1038/s41586-021-03927-z
chicago: Vercellino, Irene, and Leonid A Sazanov. “Structure and Assembly of the
Mammalian Mitochondrial Supercomplex CIII2CIV.” Nature. Springer
Nature, 2021. https://doi.org/10.1038/s41586-021-03927-z.
ieee: I. Vercellino and L. A. Sazanov, “Structure and assembly of the mammalian
mitochondrial supercomplex CIII2CIV,” Nature, vol. 598, no.
7880. Springer Nature, pp. 364–367, 2021.
ista: Vercellino I, Sazanov LA. 2021. Structure and assembly of the mammalian mitochondrial
supercomplex CIII2CIV. Nature. 598(7880), 364–367.
mla: Vercellino, Irene, and Leonid A. Sazanov. “Structure and Assembly of the Mammalian
Mitochondrial Supercomplex CIII2CIV.” Nature, vol. 598, no.
7880, Springer Nature, 2021, pp. 364–67, doi:10.1038/s41586-021-03927-z.
short: I. Vercellino, L.A. Sazanov, Nature 598 (2021) 364–367.
date_created: 2021-10-17T22:01:17Z
date_published: 2021-10-14T00:00:00Z
date_updated: 2023-08-14T08:01:21Z
day: '14'
department:
- _id: LeSa
doi: 10.1038/s41586-021-03927-z
ec_funded: 1
external_id:
isi:
- '000704581600001'
pmid:
- '34616041'
intvolume: ' 598'
isi: 1
issue: '7880'
language:
- iso: eng
month: '10'
oa_version: None
page: 364-367
pmid: 1
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: Nature
publication_identifier:
eissn:
- 1476-4687
issn:
- 0028-0836
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
link:
- description: News on IST Webpage
relation: press_release
url: https://ist.ac.at/en/news/boosting-the-cells-power-house/
scopus_import: '1'
status: public
title: Structure and assembly of the mammalian mitochondrial supercomplex CIII2CIV
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 598
year: '2021'
...
---
_id: '10148'
abstract:
- lang: eng
text: Tactile feedback of an object’s surface enables us to discern its material
properties and affordances. This understanding is used in digital fabrication
processes by creating objects with high-resolution surface variations to influence
a user’s tactile perception. As the design of such surface haptics commonly relies
on knowledge from real-life experiences, it is unclear how to adapt this information
for digital design methods. In this work, we investigate replicating the haptics
of real materials. Using an existing process for capturing an object’s microgeometry,
we digitize and reproduce the stable surface information of a set of 15 fabric
samples. In a psychophysical experiment, we evaluate the tactile qualities of
our set of original samples and their replicas. From our results, we see that
direct reproduction of surface variations is able to influence different psychophysical
dimensions of the tactile perception of surface textures. While the fabrication
process did not preserve all properties, our approach underlines that replication
of surface microgeometries benefits fabrication methods in terms of haptic perception
by covering a large range of tactile variations. Moreover, by changing the surface
structure of a single fabricated material, its material perception can be influenced.
We conclude by proposing strategies for capturing and reproducing digitized textures
to better resemble the perceived haptics of the originals.
acknowledgement: Our gratitude goes out to Kamila Mushkina, Akhmajon Makhsadov, Jordan
Espenshade, Bruno Fruchard, Roland Bennewitz, and Robert Drumm. This project has
received funding from the EU’s Horizon 2020 research and innovation programme, under
the Marie Skłodowska-Curie grant agreement No 642841 (DISTRO).
article_processing_charge: No
author:
- first_name: Donald
full_name: Degraen, Donald
last_name: Degraen
- first_name: Michael
full_name: Piovarci, Michael
id: 62E473F4-5C99-11EA-A40E-AF823DDC885E
last_name: Piovarci
- first_name: Bernd
full_name: Bickel, Bernd
id: 49876194-F248-11E8-B48F-1D18A9856A87
last_name: Bickel
orcid: 0000-0001-6511-9385
- first_name: Antonio
full_name: Kruger, Antonio
last_name: Kruger
citation:
ama: 'Degraen D, Piovarci M, Bickel B, Kruger A. Capturing tactile properties of
real surfaces for haptic reproduction. In: 34th Annual ACM Symposium. Association
for Computing Machinery; 2021:954-971. doi:10.1145/3472749.3474798'
apa: 'Degraen, D., Piovarci, M., Bickel, B., & Kruger, A. (2021). Capturing
tactile properties of real surfaces for haptic reproduction. In 34th Annual
ACM Symposium (pp. 954–971). Virtual: Association for Computing Machinery.
https://doi.org/10.1145/3472749.3474798'
chicago: Degraen, Donald, Michael Piovarci, Bernd Bickel, and Antonio Kruger. “Capturing
Tactile Properties of Real Surfaces for Haptic Reproduction.” In 34th Annual
ACM Symposium, 954–71. Association for Computing Machinery, 2021. https://doi.org/10.1145/3472749.3474798.
ieee: D. Degraen, M. Piovarci, B. Bickel, and A. Kruger, “Capturing tactile properties
of real surfaces for haptic reproduction,” in 34th Annual ACM Symposium,
Virtual, 2021, pp. 954–971.
ista: 'Degraen D, Piovarci M, Bickel B, Kruger A. 2021. Capturing tactile properties
of real surfaces for haptic reproduction. 34th Annual ACM Symposium. UIST: User
Interface Software and Technology, 954–971.'
mla: Degraen, Donald, et al. “Capturing Tactile Properties of Real Surfaces for
Haptic Reproduction.” 34th Annual ACM Symposium, Association for Computing
Machinery, 2021, pp. 954–71, doi:10.1145/3472749.3474798.
short: D. Degraen, M. Piovarci, B. Bickel, A. Kruger, in:, 34th Annual ACM Symposium,
Association for Computing Machinery, 2021, pp. 954–971.
conference:
end_date: 2021-10-14
location: Virtual
name: 'UIST: User Interface Software and Technology'
start_date: 2021-10-10
date_created: 2021-10-18T07:36:11Z
date_published: 2021-10-10T00:00:00Z
date_updated: 2021-10-19T19:29:06Z
day: '10'
ddc:
- '000'
department:
- _id: BeBi
doi: 10.1145/3472749.3474798
ec_funded: 1
file:
- access_level: open_access
checksum: b0b26464df79b3a59e8ed82e4e19ab15
content_type: application/pdf
creator: bbickel
date_created: 2021-10-18T07:36:03Z
date_updated: 2021-10-18T07:36:03Z
file_id: '10149'
file_name: degraen-UIST2021_Texture_Appropriation_CR_preprint.pdf
file_size: 29796364
relation: main_file
file_date_updated: 2021-10-18T07:36:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Preprint
page: 954-971
project:
- _id: 2508E324-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '642841'
name: Distributed 3D Object Design
publication: 34th Annual ACM Symposium
publication_identifier:
isbn:
- 978-1-4503-8635-7
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
status: public
title: Capturing tactile properties of real surfaces for haptic reproduction
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2021'
...
---
_id: '10153'
abstract:
- lang: eng
text: "Gradual typing is a principled means for mixing typed and untyped code. But
typed and untyped code often exhibit different programming patterns. There is
already substantial research investigating gradually giving types to code exhibiting
typical untyped patterns, and some research investigating gradually removing types
from code exhibiting typical typed patterns. This paper investigates how to extend
these established gradual-typing concepts to give formal guarantees not only about
how to change types as code evolves but also about how to change such programming
patterns as well.\r\n\r\nIn particular, we explore mixing untyped \"structural\"
code with typed \"nominal\" code in an object-oriented language. But whereas previous
work only allowed \"nominal\" objects to be treated as \"structural\" objects,
we also allow \"structural\" objects to dynamically acquire certain nominal types,
namely interfaces. We present a calculus that supports such \"cross-paradigm\"
code migration and interoperation in a manner satisfying both the static and dynamic
gradual guarantees, and demonstrate that the calculus can be implemented efficiently."
acknowledgement: "We thank the reviewers for their valuable suggestions towards improving
the paper. We also \r\nthank Mae Milano and Adrian Sampson, as well as the members
of the Programming Languages Discussion Group at Cornell University and of the Programming
Research Laboratory at Northeastern University, for their helpful feedback on preliminary
findings of this work.\r\n\r\nThis material is based upon work supported in part
by the National Science Foundation (NSF) through grant CCF-1350182 and the Austrian
Science Fund (FWF) through grant Z211-N23 (Wittgenstein~Award).\r\nAny opinions,
findings, and conclusions or recommendations expressed in this material are those
of the authors and do not necessarily reflect the views of the NSF or the FWF."
article_number: '127'
article_processing_charge: No
article_type: original
author:
- first_name: Fabian
full_name: Mühlböck, Fabian
id: 6395C5F6-89DF-11E9-9C97-6BDFE5697425
last_name: Mühlböck
orcid: 0000-0003-1548-0177
- first_name: Ross
full_name: Tate, Ross
last_name: Tate
citation:
ama: Mühlböck F, Tate R. Transitioning from structural to nominal code with efficient
gradual typing. Proceedings of the ACM on Programming Languages. 2021;5.
doi:10.1145/3485504
apa: 'Mühlböck, F., & Tate, R. (2021). Transitioning from structural to nominal
code with efficient gradual typing. Proceedings of the ACM on Programming Languages.
Chicago, IL, United States: Association for Computing Machinery. https://doi.org/10.1145/3485504'
chicago: Mühlböck, Fabian, and Ross Tate. “Transitioning from Structural to Nominal
Code with Efficient Gradual Typing.” Proceedings of the ACM on Programming
Languages. Association for Computing Machinery, 2021. https://doi.org/10.1145/3485504.
ieee: F. Mühlböck and R. Tate, “Transitioning from structural to nominal code with
efficient gradual typing,” Proceedings of the ACM on Programming Languages,
vol. 5. Association for Computing Machinery, 2021.
ista: Mühlböck F, Tate R. 2021. Transitioning from structural to nominal code with
efficient gradual typing. Proceedings of the ACM on Programming Languages. 5,
127.
mla: Mühlböck, Fabian, and Ross Tate. “Transitioning from Structural to Nominal
Code with Efficient Gradual Typing.” Proceedings of the ACM on Programming
Languages, vol. 5, 127, Association for Computing Machinery, 2021, doi:10.1145/3485504.
short: F. Mühlböck, R. Tate, Proceedings of the ACM on Programming Languages 5 (2021).
conference:
end_date: 2021-10-23
location: Chicago, IL, United States
name: 'OOPSLA: Object-Oriented Programming, Systems, Languages, and Applications'
start_date: 2021-10-17
date_created: 2021-10-19T12:48:44Z
date_published: 2021-10-15T00:00:00Z
date_updated: 2021-11-12T11:30:07Z
day: '15'
ddc:
- '005'
department:
- _id: ToHe
doi: 10.1145/3485504
file:
- access_level: open_access
checksum: 71011efd2da771cafdec7f0d9693f8c1
content_type: application/pdf
creator: fmuehlbo
date_created: 2021-10-19T12:52:23Z
date_updated: 2021-10-19T12:52:23Z
file_id: '10154'
file_name: monnom-oopsla21.pdf
file_size: 770269
relation: main_file
success: 1
file_date_updated: 2021-10-19T12:52:23Z
has_accepted_license: '1'
intvolume: ' 5'
keyword:
- gradual typing
- gradual guarantee
- nominal
- structural
- call tags
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nd/4.0/
month: '10'
oa: 1
oa_version: Published Version
project:
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: Z211
name: The Wittgenstein Prize
publication: Proceedings of the ACM on Programming Languages
publication_identifier:
eissn:
- 2475-1421
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
status: public
title: Transitioning from structural to nominal code with efficient gradual typing
tmp:
image: /image/cc_by_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nd/4.0/legalcode
name: Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0)
short: CC BY-ND (4.0)
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 5
year: '2021'
...
---
_id: '10163'
abstract:
- lang: eng
text: The C-terminal domain (CTD) of the largest subunit of RNA polymerase II (Pol
II) is a regulatory hub for transcription and RNA processing. Here, we identify
PHD-finger protein 3 (PHF3) as a regulator of transcription and mRNA stability
that docks onto Pol II CTD through its SPOC domain. We characterize SPOC as a
CTD reader domain that preferentially binds two phosphorylated Serine-2 marks
in adjacent CTD repeats. PHF3 drives liquid-liquid phase separation of phosphorylated
Pol II, colocalizes with Pol II clusters and tracks with Pol II across the length
of genes. PHF3 knock-out or SPOC deletion in human cells results in increased
Pol II stalling, reduced elongation rate and an increase in mRNA stability, with
marked derepression of neuronal genes. Key neuronal genes are aberrantly expressed
in Phf3 knock-out mouse embryonic stem cells, resulting in impaired neuronal differentiation.
Our data suggest that PHF3 acts as a prominent effector of neuronal gene regulation
by bridging transcription with mRNA decay.
acknowledgement: 'D.S. thanks Claudine Kraft, Renée Schroeder, Verena Jantsch, Franz
Klein and Peter Schlögelhofer for support. We thank Anita Testa Salmazo for help
with purifying Pol II; Matthias Geyer and Robert Düster for sharing DYRK1A kinase;
Felix Hartmann and Clemens Plaschka for help with mass photometry; Goran Kokic for
design of the arrest assay sequences; Petra van der Lelij for help with generating
mESC KO; Maximilian Freilinger for help with the purification of mEGFP-CTD; Stefan
Ameres, Nina Fasching and Brian Reichholf for advice on SLAM-seq and for sharing
reagents; Laura Gallego Valle for advice regarding LLPS assays; Krzysztof Chylinski
for advice regarding CRISPR/Cas9 methodology; VBCF Protein Technologies facility
for purifying PHF3 and providing gRNAs and Cas9; VBCF NGS facility for sequencing;
Monoclonal antibody facility at the Helmholtz center for Pol II antibodies; Friedrich
Propst and Elzbieta Kowalska for advice and for sharing materials; Egon Ogris for
sharing materials; Martin Eilers for recommending a ChIP-grade TFIIS antibody; Susanne
Opravil, Otto Hudecz, Markus Hartl and Natascha Hartl for mass spectrometry analysis;
staff of the X-ray beamlines at the ESRF in Grenoble for their excellent support;
Christa Bücker, Anton Meinhart, Clemens Plaschka and members of the Slade lab for
critical comments on the manuscript; Life Science Editors for editing assistance.
M.B. and D.S. acknowledge support by the FWF-funded DK ‘Chromosome Dynamics’. T.K.
is a recipient of the DOC fellowship from the Austrian Academy of Sciences. U.S.
is supported by the L’Oreal for Women in Science Austria Fellowship and the Austrian
Science Fund (FWF T 795-B30). M.L is supported by the Vienna Science and Technology
Fund (WWTF, VRG14-006). R.S. is supported by the Czech Science Foundation (15-17670 S
and 21-24460 S), Ministry of Education, Youths and Sports of the Czech Republic
(CEITEC 2020 project (LQ1601)), and the European Research Council (ERC) under the
European Union’s Horizon 2020 research and innovation programme (Grant agreement
no. 649030); this publication reflects only the author’s view and the Research Executive
Agency is not responsible for any use that may be made of the information it contains.
M.S. is supported by the Czech Science Foundation (GJ20-21581Y). K.D.C. research
is supported by the Austrian Science Fund (FWF) Projects I525 and I1593, P22276,
P19060, and W1221, Federal Ministry of Economy, Family and Youth through the initiative
‘Laura Bassi Centres of Expertise’, funding from the Centre of Optimized Structural
Studies No. 253275, the Wellcome Trust Collaborative Award (201543/Z/16), COST action
BM1405 Non-globular proteins - from sequence to structure, function and application
in molecular physiopathology (NGP-NET), the Vienna Science and Technology Fund (WWTF
LS17-008), and by the University of Vienna. This project was funded by the MFPL
start-up grant, the Vienna Science and Technology Fund (WWTF LS14-001), and the
Austrian Science Fund (P31546-B28 and W1258 “DK: Integrative Structural Biology”)
to D.S.'
article_number: '6078'
article_processing_charge: No
article_type: original
author:
- first_name: Lisa-Marie
full_name: Appel, Lisa-Marie
last_name: Appel
- first_name: Vedran
full_name: Franke, Vedran
last_name: Franke
- first_name: Melania
full_name: Bruno, Melania
last_name: Bruno
- first_name: Irina
full_name: Grishkovskaya, Irina
last_name: Grishkovskaya
- first_name: Aiste
full_name: Kasiliauskaite, Aiste
last_name: Kasiliauskaite
- first_name: Tanja
full_name: Kaufmann, Tanja
last_name: Kaufmann
- first_name: Ursula E.
full_name: Schoeberl, Ursula E.
last_name: Schoeberl
- first_name: Martin G.
full_name: Puchinger, Martin G.
last_name: Puchinger
- first_name: Sebastian
full_name: Kostrhon, Sebastian
last_name: Kostrhon
- first_name: Carmen
full_name: Ebenwaldner, Carmen
last_name: Ebenwaldner
- first_name: Marek
full_name: Sebesta, Marek
last_name: Sebesta
- first_name: Etienne
full_name: Beltzung, Etienne
last_name: Beltzung
- first_name: Karl
full_name: Mechtler, Karl
last_name: Mechtler
- first_name: Gen
full_name: Lin, Gen
last_name: Lin
- first_name: Anna
full_name: Vlasova, Anna
last_name: Vlasova
- first_name: Martin
full_name: Leeb, Martin
last_name: Leeb
- first_name: Rushad
full_name: Pavri, Rushad
last_name: Pavri
- first_name: Alexander
full_name: Stark, Alexander
last_name: Stark
- first_name: Altuna
full_name: Akalin, Altuna
last_name: Akalin
- first_name: Richard
full_name: Stefl, Richard
last_name: Stefl
- first_name: Carrie A
full_name: Bernecky, Carrie A
id: 2CB9DFE2-F248-11E8-B48F-1D18A9856A87
last_name: Bernecky
orcid: 0000-0003-0893-7036
- first_name: Kristina
full_name: Djinovic-Carugo, Kristina
last_name: Djinovic-Carugo
- first_name: Dea
full_name: Slade, Dea
last_name: Slade
citation:
ama: Appel L-M, Franke V, Bruno M, et al. PHF3 regulates neuronal gene expression
through the Pol II CTD reader domain SPOC. Nature Communications. 2021;12(1).
doi:10.1038/s41467-021-26360-2
apa: Appel, L.-M., Franke, V., Bruno, M., Grishkovskaya, I., Kasiliauskaite, A.,
Kaufmann, T., … Slade, D. (2021). PHF3 regulates neuronal gene expression through
the Pol II CTD reader domain SPOC. Nature Communications. Springer Nature.
https://doi.org/10.1038/s41467-021-26360-2
chicago: Appel, Lisa-Marie, Vedran Franke, Melania Bruno, Irina Grishkovskaya, Aiste
Kasiliauskaite, Tanja Kaufmann, Ursula E. Schoeberl, et al. “PHF3 Regulates Neuronal
Gene Expression through the Pol II CTD Reader Domain SPOC.” Nature Communications.
Springer Nature, 2021. https://doi.org/10.1038/s41467-021-26360-2.
ieee: L.-M. Appel et al., “PHF3 regulates neuronal gene expression through
the Pol II CTD reader domain SPOC,” Nature Communications, vol. 12, no.
1. Springer Nature, 2021.
ista: Appel L-M, Franke V, Bruno M, Grishkovskaya I, Kasiliauskaite A, Kaufmann
T, Schoeberl UE, Puchinger MG, Kostrhon S, Ebenwaldner C, Sebesta M, Beltzung
E, Mechtler K, Lin G, Vlasova A, Leeb M, Pavri R, Stark A, Akalin A, Stefl R,
Bernecky C, Djinovic-Carugo K, Slade D. 2021. PHF3 regulates neuronal gene expression
through the Pol II CTD reader domain SPOC. Nature Communications. 12(1), 6078.
mla: Appel, Lisa-Marie, et al. “PHF3 Regulates Neuronal Gene Expression through
the Pol II CTD Reader Domain SPOC.” Nature Communications, vol. 12, no.
1, 6078, Springer Nature, 2021, doi:10.1038/s41467-021-26360-2.
short: L.-M. Appel, V. Franke, M. Bruno, I. Grishkovskaya, A. Kasiliauskaite, T.
Kaufmann, U.E. Schoeberl, M.G. Puchinger, S. Kostrhon, C. Ebenwaldner, M. Sebesta,
E. Beltzung, K. Mechtler, G. Lin, A. Vlasova, M. Leeb, R. Pavri, A. Stark, A.
Akalin, R. Stefl, C. Bernecky, K. Djinovic-Carugo, D. Slade, Nature Communications
12 (2021).
date_created: 2021-10-20T14:40:32Z
date_published: 2021-10-19T00:00:00Z
date_updated: 2023-08-14T08:02:31Z
day: '19'
ddc:
- '610'
department:
- _id: CaBe
doi: 10.1038/s41467-021-26360-2
external_id:
isi:
- '000709050300001'
file:
- access_level: open_access
checksum: d99fcd51aebde19c21314e3de0148007
content_type: application/pdf
creator: cchlebak
date_created: 2021-10-21T13:51:49Z
date_updated: 2021-10-21T13:51:49Z
file_id: '10169'
file_name: 2021_NatComm_Appel.pdf
file_size: 5111706
relation: main_file
success: 1
file_date_updated: 2021-10-21T13:51:49Z
has_accepted_license: '1'
intvolume: ' 12'
isi: 1
issue: '1'
keyword:
- general physics and astronomy
- general biochemistry
- genetics and molecular biology
- general chemistry
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
publication: Nature Communications
publication_identifier:
eissn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
link:
- description: 'Preprint '
relation: earlier_version
url: https://www.biorxiv.org/content/10.1101/2020.02.11.943159
status: public
title: PHF3 regulates neuronal gene expression through the Pol II CTD reader domain
SPOC
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: 12
year: '2021'
...
---
_id: '10166'
abstract:
- lang: eng
text: While sexual reproduction is widespread among many taxa, asexual lineages
have repeatedly evolved from sexual ancestors. Despite extensive research on the
evolution of sex, it is still unclear whether this switch represents a major transition
requiring major molecular reorganization, and how convergent the changes involved
are. In this study, we investigated the phylogenetic relationship and patterns
of gene expression of sexual and asexual lineages of Eurasian Artemia brine shrimp,
to assess how gene expression patterns are affected by the transition to asexuality.
We find only a few genes that are consistently associated with the evolution of
asexuality, suggesting that this shift may not require an extensive overhauling
of the meiotic machinery. While genes with sex-biased expression have high rates
of expression divergence within Eurasian Artemia, neither female- nor male-biased
genes appear to show unusual evolutionary patterns after sexuality is lost, contrary
to theoretical expectations.
acknowledged_ssus:
- _id: ScienComp
acknowledgement: We thank the Vicoso laboratory, Thomas Lenormand and Tanja Schwander
for helpful discussions, the group of Gonzalo Gajardo, especially Cristian Gallardo-Escárate
and Margarita Parraguez Donoso, for sequencing data and advice, and the IST Scientific
Computing Group for their support. This work was supported by the European Research
Council under the European Union's Horizon 2020 research and innovation program
(grant agreement no. 715257).
article_number: '20211720'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Ann K
full_name: Huylmans, Ann K
id: 4C0A3874-F248-11E8-B48F-1D18A9856A87
last_name: Huylmans
orcid: 0000-0001-8871-4961
- first_name: Ariana
full_name: Macon, Ariana
id: 2A0848E2-F248-11E8-B48F-1D18A9856A87
last_name: Macon
- first_name: Francisco
full_name: Hontoria, Francisco
last_name: Hontoria
- first_name: Beatriz
full_name: Vicoso, Beatriz
id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
last_name: Vicoso
orcid: 0000-0002-4579-8306
citation:
ama: 'Huylmans AK, Macon A, Hontoria F, Vicoso B. Transitions to asexuality and
evolution of gene expression in Artemia brine shrimp. Proceedings of the Royal
Society B: Biological Sciences. 2021;288(1959). doi:10.1098/rspb.2021.1720'
apa: 'Huylmans, A. K., Macon, A., Hontoria, F., & Vicoso, B. (2021). Transitions
to asexuality and evolution of gene expression in Artemia brine shrimp. Proceedings
of the Royal Society B: Biological Sciences. The Royal Society. https://doi.org/10.1098/rspb.2021.1720'
chicago: 'Huylmans, Ann K, Ariana Macon, Francisco Hontoria, and Beatriz Vicoso.
“Transitions to Asexuality and Evolution of Gene Expression in Artemia Brine Shrimp.”
Proceedings of the Royal Society B: Biological Sciences. The Royal Society,
2021. https://doi.org/10.1098/rspb.2021.1720.'
ieee: 'A. K. Huylmans, A. Macon, F. Hontoria, and B. Vicoso, “Transitions to asexuality
and evolution of gene expression in Artemia brine shrimp,” Proceedings of the
Royal Society B: Biological Sciences, vol. 288, no. 1959. The Royal Society,
2021.'
ista: 'Huylmans AK, Macon A, Hontoria F, Vicoso B. 2021. Transitions to asexuality
and evolution of gene expression in Artemia brine shrimp. Proceedings of the Royal
Society B: Biological Sciences. 288(1959), 20211720.'
mla: 'Huylmans, Ann K., et al. “Transitions to Asexuality and Evolution of Gene
Expression in Artemia Brine Shrimp.” Proceedings of the Royal Society B: Biological
Sciences, vol. 288, no. 1959, 20211720, The Royal Society, 2021, doi:10.1098/rspb.2021.1720.'
short: 'A.K. Huylmans, A. Macon, F. Hontoria, B. Vicoso, Proceedings of the Royal
Society B: Biological Sciences 288 (2021).'
date_created: 2021-10-21T07:46:06Z
date_published: 2021-09-22T00:00:00Z
date_updated: 2024-02-21T12:40:29Z
day: '22'
ddc:
- '595'
department:
- _id: BeVi
doi: 10.1098/rspb.2021.1720
ec_funded: 1
external_id:
isi:
- '000697643700001'
pmid:
- '34547909'
file:
- access_level: open_access
checksum: 76e7f253b7040bca2ad76f82bd7c45c0
content_type: application/pdf
creator: cchlebak
date_created: 2021-10-22T11:48:02Z
date_updated: 2021-10-22T11:48:02Z
file_id: '10172'
file_name: 2021_ProRoSocBBioSci_Huylmans.pdf
file_size: 995806
relation: main_file
success: 1
file_date_updated: 2021-10-22T11:48:02Z
has_accepted_license: '1'
intvolume: ' 288'
isi: 1
issue: '1959'
keyword:
- asexual reproduction
- parthenogenesis
- sex-biased genes
- sexual conflict
- automixis
- crustaceans
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 250BDE62-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '715257'
name: Prevalence and Influence of Sexual Antagonism on Genome Evolution
publication: 'Proceedings of the Royal Society B: Biological Sciences'
publication_identifier:
eissn:
- 1471-2954
issn:
- 0962-8452
publication_status: published
publisher: The Royal Society
quality_controlled: '1'
related_material:
link:
- relation: supplementary_material
url: https://doi.org/10.6084/m9.figshare.c.5615488.v1
record:
- id: '9949'
relation: research_data
status: public
scopus_import: '1'
status: public
title: Transitions to asexuality and evolution of gene expression in Artemia brine
shrimp
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: 288
year: '2021'
...
---
_id: '10167'
abstract:
- lang: eng
text: Schistosomes, the human parasites responsible for snail fever, are female-heterogametic.
Different parts of their ZW sex chromosomes have stopped recombining in distinct
lineages, creating “evolutionary strata” of various ages. Although the Z-chromosome
is well characterized at the genomic and molecular level, the W-chromosome has
remained largely unstudied from an evolutionary perspective, as only a few W-linked
genes have been detected outside of the model species Schistosoma mansoni. Here,
we characterize the gene content and evolution of the W-chromosomes of S. mansoni
and of the divergent species S. japonicum. We use a combined RNA/DNA k-mer based
pipeline to assemble around 100 candidate W-specific transcripts in each of the
species. About half of them map to known protein coding genes, the majority homologous
to S. mansoni Z-linked genes. We perform an extended analysis of the evolutionary
strata present in the two species (including characterizing a previously undetected
young stratum in S. japonicum) to infer patterns of sequence and expression evolution
of W-linked genes at different time points after recombination was lost. W-linked
genes show evidence of degeneration, including high rates of protein evolution
and reduced expression. Most are found in young lineage-specific strata, with
only a few high expression ancestral W-genes remaining, consistent with the progressive
erosion of nonrecombining regions. Among these, the splicing factor u2af2 stands
out as a promising candidate for primary sex determination, opening new avenues
for understanding the molecular basis of the reproductive biology of this group.
acknowledged_ssus:
- _id: ScienComp
acknowledgement: The authors thank IT support at IST Austria for providing an optimal
environment for bioinformatic analyses. This work was supported by an Austrian Science
Foundation FWF grant (Project P28842) to B.V.
article_processing_charge: No
article_type: original
author:
- first_name: Marwan N
full_name: Elkrewi, Marwan N
id: 0B46FACA-A8E1-11E9-9BD3-79D1E5697425
last_name: Elkrewi
orcid: 0000-0002-5328-7231
- first_name: Mikhail A.
full_name: Moldovan, Mikhail A.
id: c8bb7f32-3315-11ec-b58b-e5950e6c14a0
last_name: Moldovan
orcid: 0000-0002-8876-6494
- first_name: Marion A L
full_name: Picard, Marion A L
id: 2C921A7A-F248-11E8-B48F-1D18A9856A87
last_name: Picard
orcid: 0000-0002-8101-2518
- first_name: Beatriz
full_name: Vicoso, Beatriz
id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
last_name: Vicoso
orcid: 0000-0002-4579-8306
citation:
ama: Elkrewi MN, Moldovan MA, Picard MAL, Vicoso B. Schistosome W-Linked genes inform
temporal dynamics of sex chromosome evolution and suggest candidate for sex determination.
Molecular Biology and Evolution. 2021. doi:10.1093/molbev/msab178
apa: Elkrewi, M. N., Moldovan, M. A., Picard, M. A. L., & Vicoso, B. (2021).
Schistosome W-Linked genes inform temporal dynamics of sex chromosome evolution
and suggest candidate for sex determination. Molecular Biology and Evolution.
Oxford University Press . https://doi.org/10.1093/molbev/msab178
chicago: Elkrewi, Marwan N, Mikhail A. Moldovan, Marion A L Picard, and Beatriz
Vicoso. “Schistosome W-Linked Genes Inform Temporal Dynamics of Sex Chromosome
Evolution and Suggest Candidate for Sex Determination.” Molecular Biology and
Evolution. Oxford University Press , 2021. https://doi.org/10.1093/molbev/msab178.
ieee: M. N. Elkrewi, M. A. Moldovan, M. A. L. Picard, and B. Vicoso, “Schistosome
W-Linked genes inform temporal dynamics of sex chromosome evolution and suggest
candidate for sex determination,” Molecular Biology and Evolution. Oxford
University Press , 2021.
ista: Elkrewi MN, Moldovan MA, Picard MAL, Vicoso B. 2021. Schistosome W-Linked
genes inform temporal dynamics of sex chromosome evolution and suggest candidate
for sex determination. Molecular Biology and Evolution.
mla: Elkrewi, Marwan N., et al. “Schistosome W-Linked Genes Inform Temporal Dynamics
of Sex Chromosome Evolution and Suggest Candidate for Sex Determination.” Molecular
Biology and Evolution, Oxford University Press , 2021, doi:10.1093/molbev/msab178.
short: M.N. Elkrewi, M.A. Moldovan, M.A.L. Picard, B. Vicoso, Molecular Biology
and Evolution (2021).
date_created: 2021-10-21T07:49:12Z
date_published: 2021-06-19T00:00:00Z
date_updated: 2023-08-14T08:03:06Z
day: '19'
ddc:
- '610'
department:
- _id: BeVi
doi: 10.1093/molbev/msab178
external_id:
isi:
- '000741368600009'
pmid:
- '34146097'
file:
- access_level: open_access
checksum: 1b096702fb356d9c0eb88e1b3fcff5f8
content_type: application/pdf
creator: dernst
date_created: 2022-05-06T09:47:18Z
date_updated: 2022-05-06T09:47:18Z
file_id: '11352'
file_name: 2021_MolecularBiolEvolution_Elkrewi.pdf
file_size: 1008594
relation: main_file
success: 1
file_date_updated: 2022-05-06T09:47:18Z
has_accepted_license: '1'
isi: 1
keyword:
- sex chromosomes
- evolutionary strata
- W-linked gene
- sex determining gene
- schistosome parasites
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 250ED89C-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P28842-B22
name: Sex chromosome evolution under male- and female- heterogamety
publication: Molecular Biology and Evolution
publication_identifier:
eissn:
- 1537-1719
issn:
- 0737-4038
publication_status: published
publisher: 'Oxford University Press '
quality_controlled: '1'
scopus_import: '1'
status: public
title: Schistosome W-Linked genes inform temporal dynamics of sex chromosome evolution
and suggest candidate for sex determination
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
year: '2021'
...
---
_id: '10174'
abstract:
- lang: eng
text: Quantitative stochastic homogenization of linear elliptic operators is by
now well-understood. In this contribution we move forward to the nonlinear setting
of monotone operators with p-growth. This first work is dedicated to a quantitative
two-scale expansion result. Fluctuations will be addressed in companion articles.
By treating the range of exponents 2≤p<∞ in dimensions d≤3, we are able to consider
genuinely nonlinear elliptic equations and systems such as −∇⋅A(x)(1+|∇u|p−2)∇u=f
(with A random, non-necessarily symmetric) for the first time. When going from
p=2 to p>2, the main difficulty is to analyze the associated linearized operator,
whose coefficients are degenerate, unbounded, and depend on the random input A
via the solution of a nonlinear equation. One of our main achievements is the
control of this intricate nonlinear dependence, leading to annealed Meyers' estimates
for the linearized operator, which are key to the quantitative two-scale expansion
result.
acknowledgement: The authors warmly thank Mitia Duerinckx for discussions on annealed
estimates, and Mathias Schäffner for pointing out that the conditions of [14] apply
to ̄a in the setting of Theorem 2.2 and for discussions on regularity theory for
operators with non-standard growth conditions. The authors received financial support
from the European Research Council (ERC) under the European Union’s Horizon 2020
research and innovation programme (Grant Agreement n◦ 864066).
article_number: '2104.04263'
article_processing_charge: No
arxiv: 1
author:
- first_name: Nicolas
full_name: Clozeau, Nicolas
id: fea1b376-906f-11eb-847d-b2c0cf46455b
last_name: Clozeau
- first_name: Antoine
full_name: Gloria, Antoine
last_name: Gloria
citation:
ama: 'Clozeau N, Gloria A. Quantitative nonlinear homogenization: control of oscillations.
arXiv.'
apa: 'Clozeau, N., & Gloria, A. (n.d.). Quantitative nonlinear homogenization:
control of oscillations. arXiv.'
chicago: 'Clozeau, Nicolas, and Antoine Gloria. “Quantitative Nonlinear Homogenization:
Control of Oscillations.” ArXiv, n.d.'
ieee: 'N. Clozeau and A. Gloria, “Quantitative nonlinear homogenization: control
of oscillations,” arXiv. .'
ista: 'Clozeau N, Gloria A. Quantitative nonlinear homogenization: control of oscillations.
arXiv, 2104.04263.'
mla: 'Clozeau, Nicolas, and Antoine Gloria. “Quantitative Nonlinear Homogenization:
Control of Oscillations.” ArXiv, 2104.04263.'
short: N. Clozeau, A. Gloria, ArXiv (n.d.).
date_created: 2021-10-23T10:50:55Z
date_published: 2021-04-09T00:00:00Z
date_updated: 2021-10-28T15:44:05Z
day: '09'
department:
- _id: JuFi
external_id:
arxiv:
- '2104.04263'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/2104.04263
month: '04'
oa: 1
oa_version: Preprint
publication: arXiv
publication_status: submitted
status: public
title: 'Quantitative nonlinear homogenization: control of oscillations'
type: preprint
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
year: '2021'
...
---
_id: '10176'
abstract:
- lang: eng
text: "We give a combinatorial model for r-spin surfaces with parameterized boundary
based on Novak (“Lattice topological field theories in two dimensions,” Ph.D.
thesis, Universität Hamburg, 2015). The r-spin structure is encoded in terms of
ℤ\U0001D45F-valued indices assigned to the edges of a polygonal decomposition.
This combinatorial model is designed for our state-sum construction of two-dimensional
topological field theories on r-spin surfaces. We show that an example of such
a topological field theory computes the Arf-invariant of an r-spin surface as
introduced by Randal-Williams [J. Topol. 7, 155 (2014)] and Geiges et al. [Osaka
J. Math. 49, 449 (2012)]. This implies, in particular, that the r-spin Arf-invariant
is constant on orbits of the mapping class group, providing an alternative proof
of that fact."
acknowledgement: We would like to thank Nils Carqueville, Tobias Dyckerhoff, Jan Hesse,
Ehud Meir, Sebastian Novak, Louis-Hadrien Robert, Nick Salter, Walker Stern, and
Lukas Woike for helpful discussions and comments. L.S. was supported by the DFG
Research Training Group 1670 “Mathematics Inspired by String Theory and Quantum
Field Theory.”
article_number: '102302'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Ingo
full_name: Runkel, Ingo
last_name: Runkel
- first_name: Lorant
full_name: Szegedy, Lorant
id: 7943226E-220E-11EA-94C7-D59F3DDC885E
last_name: Szegedy
orcid: 0000-0003-2834-5054
citation:
ama: Runkel I, Szegedy L. Topological field theory on r-spin surfaces and the Arf-invariant.
Journal of Mathematical Physics. 2021;62(10). doi:10.1063/5.0037826
apa: Runkel, I., & Szegedy, L. (2021). Topological field theory on r-spin surfaces
and the Arf-invariant. Journal of Mathematical Physics. AIP Publishing.
https://doi.org/10.1063/5.0037826
chicago: Runkel, Ingo, and Lorant Szegedy. “Topological Field Theory on R-Spin Surfaces
and the Arf-Invariant.” Journal of Mathematical Physics. AIP Publishing,
2021. https://doi.org/10.1063/5.0037826.
ieee: I. Runkel and L. Szegedy, “Topological field theory on r-spin surfaces and
the Arf-invariant,” Journal of Mathematical Physics, vol. 62, no. 10. AIP
Publishing, 2021.
ista: Runkel I, Szegedy L. 2021. Topological field theory on r-spin surfaces and
the Arf-invariant. Journal of Mathematical Physics. 62(10), 102302.
mla: Runkel, Ingo, and Lorant Szegedy. “Topological Field Theory on R-Spin Surfaces
and the Arf-Invariant.” Journal of Mathematical Physics, vol. 62, no. 10,
102302, AIP Publishing, 2021, doi:10.1063/5.0037826.
short: I. Runkel, L. Szegedy, Journal of Mathematical Physics 62 (2021).
date_created: 2021-10-24T22:01:32Z
date_published: 2021-10-01T00:00:00Z
date_updated: 2023-08-14T08:04:12Z
day: '01'
department:
- _id: MiLe
doi: 10.1063/5.0037826
external_id:
arxiv:
- '1802.09978'
isi:
- '000755638500010'
intvolume: ' 62'
isi: 1
issue: '10'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1802.09978
month: '10'
oa: 1
oa_version: Preprint
publication: Journal of Mathematical Physics
publication_identifier:
issn:
- '00222488'
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Topological field theory on r-spin surfaces and the Arf-invariant
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 62
year: '2021'
...
---
_id: '10177'
abstract:
- lang: eng
text: Phonon polaritons (PhPs)—light coupled to lattice vibrations—with in-plane
hyperbolic dispersion exhibit ray-like propagation with large wave vectors and
enhanced density of optical states along certain directions on a surface. As such,
they have raised a surge of interest, promising unprecedented manipulation of
infrared light at the nanoscale in a planar circuitry. Here, we demonstrate focusing
of in-plane hyperbolic PhPs propagating along thin slabs of α-MoO3. To that end,
we developed metallic nanoantennas of convex geometries for both efficient launching
and focusing of the polaritons. The foci obtained exhibit enhanced near-field
confinement and absorption compared to foci produced by in-plane isotropic PhPs.
Foci sizes as small as λp/4.5 = λ0/50 were achieved (λp is the polariton wavelength
and λ0 is the photon wavelength). Focusing of in-plane hyperbolic polaritons introduces
a first and most basic building block developing planar polariton optics using
in-plane anisotropic van der Waals materials.
acknowledgement: J.M.-S. acknowledges financial support from the Ramón y Cajal Program
of the Government of Spain and FSE (RYC2018-026196-I) and the Spanish Ministry of
Science and Innovation (State Plan for Scientific and Technical Research and Innovation
grant number PID2019-110308GA-I00). P.A.-G. acknowledges support from the European
Research Council under starting grant no. 715496, 2DNANOPTICA, and the Spanish Ministry
of Science and Innovation (State Plan for Scientific and Technical Research and
Innovation grant number PID2019-111156GB-I00). J.T.-G. acknowledges support through
the Severo Ochoa Program from the Government of the Principality of Asturias (PA-18-PF-BP17-126).
G.A.-P. acknowledges support through the Severo Ochoa Program from the Government
of the Principality of Asturias (PA-20-PF-BP19-053). K.V.V. and V.S.V. acknowledge
the financial support from the Ministry of Science and Higher Education of the Russian
Federation (agreement no. 075-15-2021-606). A.Y.N. acknowledges the Spanish Ministry
of Science, Innovation, and Universities (national projects MAT2017-88358-C3-3-R
and PID2020-115221GB-C42) and the Basque Department of Education (PIBA-2020-1-0014).
R.H. acknowledges financial support from the Spanish Ministry of Science, Innovation,
and Universities (national project number RTI2018-094830-B-100 and project number
MDM-2016-0618 of the Marie de Maeztu Units of Excellence Program) and the Basque
Government (grant number IT1164-19).
article_number: abj0127
article_processing_charge: Yes
article_type: original
arxiv: 1
author:
- first_name: Javier
full_name: Martín-Sánchez, Javier
last_name: Martín-Sánchez
- first_name: Jiahua
full_name: Duan, Jiahua
last_name: Duan
- first_name: Javier
full_name: Taboada-Gutiérrez, Javier
last_name: Taboada-Gutiérrez
- first_name: Gonzalo
full_name: Álvarez-Pérez, Gonzalo
last_name: Álvarez-Pérez
- first_name: Kirill V.
full_name: Voronin, Kirill V.
last_name: Voronin
- first_name: Ivan
full_name: Prieto Gonzalez, Ivan
id: 2A307FE2-F248-11E8-B48F-1D18A9856A87
last_name: Prieto Gonzalez
orcid: 0000-0002-7370-5357
- first_name: Weiliang
full_name: Ma, Weiliang
last_name: Ma
- first_name: Qiaoliang
full_name: Bao, Qiaoliang
last_name: Bao
- first_name: Valentyn S.
full_name: Volkov, Valentyn S.
last_name: Volkov
- first_name: Rainer
full_name: Hillenbrand, Rainer
last_name: Hillenbrand
- first_name: Alexey Y.
full_name: Nikitin, Alexey Y.
last_name: Nikitin
- first_name: Pablo
full_name: Alonso-González, Pablo
last_name: Alonso-González
citation:
ama: Martín-Sánchez J, Duan J, Taboada-Gutiérrez J, et al. Focusing of in-plane
hyperbolic polaritons in van der Waals crystals with tailored infrared nanoantennas.
Science Advances. 2021;7(41). doi:10.1126/sciadv.abj0127
apa: Martín-Sánchez, J., Duan, J., Taboada-Gutiérrez, J., Álvarez-Pérez, G., Voronin,
K. V., Prieto Gonzalez, I., … Alonso-González, P. (2021). Focusing of in-plane
hyperbolic polaritons in van der Waals crystals with tailored infrared nanoantennas.
Science Advances. American Association for the Advancement of Science.
https://doi.org/10.1126/sciadv.abj0127
chicago: Martín-Sánchez, Javier, Jiahua Duan, Javier Taboada-Gutiérrez, Gonzalo
Álvarez-Pérez, Kirill V. Voronin, Ivan Prieto Gonzalez, Weiliang Ma, et al. “Focusing
of In-Plane Hyperbolic Polaritons in van Der Waals Crystals with Tailored Infrared
Nanoantennas.” Science Advances. American Association for the Advancement
of Science, 2021. https://doi.org/10.1126/sciadv.abj0127.
ieee: J. Martín-Sánchez et al., “Focusing of in-plane hyperbolic polaritons
in van der Waals crystals with tailored infrared nanoantennas,” Science Advances,
vol. 7, no. 41. American Association for the Advancement of Science, 2021.
ista: Martín-Sánchez J, Duan J, Taboada-Gutiérrez J, Álvarez-Pérez G, Voronin KV,
Prieto Gonzalez I, Ma W, Bao Q, Volkov VS, Hillenbrand R, Nikitin AY, Alonso-González
P. 2021. Focusing of in-plane hyperbolic polaritons in van der Waals crystals
with tailored infrared nanoantennas. Science Advances. 7(41), abj0127.
mla: Martín-Sánchez, Javier, et al. “Focusing of In-Plane Hyperbolic Polaritons
in van Der Waals Crystals with Tailored Infrared Nanoantennas.” Science Advances,
vol. 7, no. 41, abj0127, American Association for the Advancement of Science,
2021, doi:10.1126/sciadv.abj0127.
short: J. Martín-Sánchez, J. Duan, J. Taboada-Gutiérrez, G. Álvarez-Pérez, K.V.
Voronin, I. Prieto Gonzalez, W. Ma, Q. Bao, V.S. Volkov, R. Hillenbrand, A.Y.
Nikitin, P. Alonso-González, Science Advances 7 (2021).
date_created: 2021-10-24T22:01:33Z
date_published: 2021-10-08T00:00:00Z
date_updated: 2023-08-14T08:04:42Z
day: '08'
ddc:
- '530'
department:
- _id: NanoFab
doi: 10.1126/sciadv.abj0127
external_id:
arxiv:
- '2103.10852'
isi:
- '000704912700024'
file:
- access_level: open_access
checksum: 0a470ef6a47d2b8a96ede4c4d28cfacd
content_type: application/pdf
creator: cziletti
date_created: 2021-10-27T14:16:06Z
date_updated: 2021-10-27T14:16:06Z
file_id: '10189'
file_name: 2021_ScienceAdv_Martin-Sanchez.pdf
file_size: 2441163
relation: main_file
success: 1
file_date_updated: 2021-10-27T14:16:06Z
has_accepted_license: '1'
intvolume: ' 7'
isi: 1
issue: '41'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/4.0/
month: '10'
oa: 1
oa_version: Published Version
publication: Science Advances
publication_identifier:
eissn:
- '23752548'
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Focusing of in-plane hyperbolic polaritons in van der Waals crystals with tailored
infrared nanoantennas
tmp:
image: /images/cc_by_nc.png
legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
short: CC BY-NC (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 7
year: '2021'
...
---
_id: '10178'
abstract:
- lang: eng
text: In dense biological tissues, cell types performing different roles remain
segregated by maintaining sharp interfaces. To better understand the mechanisms
for such sharp compartmentalization, we study the effect of an imposed heterotypic
tension at the interface between two distinct cell types in a fully 3D Voronoi
model for confluent tissues. We find that cells rapidly sort and self-organize
to generate a tissue-scale interface between cell types, and cells adjacent to
this interface exhibit signature geometric features including nematic-like ordering,
bimodal facet areas, and registration, or alignment, of cell centers on either
side of the two-tissue interface. The magnitude of these features scales directly
with the magnitude of the imposed tension, suggesting that biologists can estimate
the magnitude of tissue surface tension between two tissue types simply by segmenting
a 3D tissue. To uncover the underlying physical mechanisms driving these geometric
features, we develop two minimal, ordered models using two different underlying
lattices that identify an energetic competition between bulk cell shapes and tissue
interface area. When the interface area dominates, changes to neighbor topology
are costly and occur less frequently, which generates the observed geometric features.
acknowledgement: "We thank Paula Sanematsu, Matthias Merkel, Daniel Sussman, Cristina
Marchetti and Edouard Hannezo for helpful discussions, and M Merkel for developing
and sharing the original version of the 3D Voronoi code. This work was primarily
funded by NSF-PHY-1607416, NSF-PHY-2014192 , and are in the division of physics
at the National Science Foundation. PS and MLM acknowledge additional support from
Simons Grant No. 454947.\r\n"
article_number: '093043'
article_processing_charge: Yes
article_type: original
arxiv: 1
author:
- first_name: Preeti
full_name: Sahu, Preeti
id: 55BA52EE-A185-11EA-88FD-18AD3DDC885E
last_name: Sahu
- first_name: J. M.
full_name: Schwarz, J. M.
last_name: Schwarz
- first_name: M. Lisa
full_name: Manning, M. Lisa
last_name: Manning
citation:
ama: Sahu P, Schwarz JM, Manning ML. Geometric signatures of tissue surface tension
in a three-dimensional model of confluent tissue. New Journal of Physics.
2021;23(9). doi:10.1088/1367-2630/ac23f1
apa: Sahu, P., Schwarz, J. M., & Manning, M. L. (2021). Geometric signatures
of tissue surface tension in a three-dimensional model of confluent tissue. New
Journal of Physics. IOP Publishing. https://doi.org/10.1088/1367-2630/ac23f1
chicago: Sahu, Preeti, J. M. Schwarz, and M. Lisa Manning. “Geometric Signatures
of Tissue Surface Tension in a Three-Dimensional Model of Confluent Tissue.” New
Journal of Physics. IOP Publishing, 2021. https://doi.org/10.1088/1367-2630/ac23f1.
ieee: P. Sahu, J. M. Schwarz, and M. L. Manning, “Geometric signatures of tissue
surface tension in a three-dimensional model of confluent tissue,” New Journal
of Physics, vol. 23, no. 9. IOP Publishing, 2021.
ista: Sahu P, Schwarz JM, Manning ML. 2021. Geometric signatures of tissue surface
tension in a three-dimensional model of confluent tissue. New Journal of Physics.
23(9), 093043.
mla: Sahu, Preeti, et al. “Geometric Signatures of Tissue Surface Tension in a Three-Dimensional
Model of Confluent Tissue.” New Journal of Physics, vol. 23, no. 9, 093043,
IOP Publishing, 2021, doi:10.1088/1367-2630/ac23f1.
short: P. Sahu, J.M. Schwarz, M.L. Manning, New Journal of Physics 23 (2021).
date_created: 2021-10-24T22:01:34Z
date_published: 2021-09-29T00:00:00Z
date_updated: 2023-08-14T08:10:31Z
day: '29'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1088/1367-2630/ac23f1
external_id:
arxiv:
- '2102.05397'
isi:
- '000702042400001'
file:
- access_level: open_access
checksum: ace603e8f0962b3ba55f23fa34f57764
content_type: application/pdf
creator: cziletti
date_created: 2021-10-28T12:06:01Z
date_updated: 2021-10-28T12:06:01Z
file_id: '10193'
file_name: 2021_NewJPhys_Sahu.pdf
file_size: 2215016
relation: main_file
success: 1
file_date_updated: 2021-10-28T12:06:01Z
has_accepted_license: '1'
intvolume: ' 23'
isi: 1
issue: '9'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
publication: New Journal of Physics
publication_identifier:
eissn:
- '13672630'
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Geometric signatures of tissue surface tension in a three-dimensional model
of confluent tissue
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: 23
year: '2021'
...
---
_id: '10179'
abstract:
- lang: eng
text: Inhibitory GABAergic interneurons migrate over long distances from their extracortical
origin into the developing cortex. In humans, this process is uniquely slow and
prolonged, and it is unclear whether guidance cues unique to humans govern the
various phases of this complex developmental process. Here, we use fused cerebral
organoids to identify key roles of neurotransmitter signaling pathways in guiding
the migratory behavior of human cortical interneurons. We use scRNAseq to reveal
expression of GABA, glutamate, glycine, and serotonin receptors along distinct
maturation trajectories across interneuron migration. We develop an image analysis
software package, TrackPal, to simultaneously assess 48 parameters for entire
migration tracks of individual cells. By chemical screening, we show that different
modes of interneuron migration depend on distinct neurotransmitter signaling pathways,
linking transcriptional maturation of interneurons with their migratory behavior.
Altogether, our study provides a comprehensive quantitative analysis of human
interneuron migration and its functional modulation by neurotransmitter signaling.
acknowledgement: We thank all Knoblich laboratory members for continued support and
discussions. We thank the IMP/IMBA BioOptics facility, particularly Pawel Pasierbek,
Alberto Moreno Cencerrado and Gerald Schmauss, the IMP/IMBA Molecular Biology Service,
in particular Robert Heinen, the IMP Bioinformatics facility, in particular Thomas
Burkard, the Vienna Biocenter Core Facilities (VBCF) Histopathology facility, in
particular Tamara Engelmaier, and the VBCF Next Generation Sequencing Facility,
notably Volodymyr Shubchynskyy and Carmen Czepe. We would also like to thank Simon
Haendeler for advice on statistical analyses, Jose Guzman for discussions and assistance
with slice culture setups, Oliver L. Eichmueller for discussions and assistance
with microscopy, and E.H. Gustafson, S. Wolfinger, and D. Reumann for technical
assistance regarding generation of cerebral organoids. This project received funding
from the European Union’s Horizon 2020 research and innovation program under the
Marie Skłodowska-Curie fellowship agreement Nr.707109 awarded to J.A.B. Work in
J.A.K.'s laboratory is supported by the Austrian Federal Ministry of Education,
Science and Research, the Austrian Academy of Sciences, the City of Vienna, a Research
Program of the Austrian Science Fund FWF (SFBF78 Stem Cell, F 7803-B) and a European
Research Council (ERC) Advanced Grant under the European 20 Union’s Horizon 2020
program (grant agreement no. 695642).
article_number: e108714
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Sunanjay
full_name: Bajaj, Sunanjay
last_name: Bajaj
- first_name: Joshua A.
full_name: Bagley, Joshua A.
last_name: Bagley
- 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: Abel
full_name: Vertesy, Abel
last_name: Vertesy
- first_name: Sakurako
full_name: Nagumo Wong, Sakurako
last_name: Nagumo Wong
- first_name: Veronica
full_name: Krenn, Veronica
last_name: Krenn
- first_name: Julie
full_name: Lévi-Strauss, Julie
last_name: Lévi-Strauss
- first_name: Juergen A.
full_name: Knoblich, Juergen A.
last_name: Knoblich
citation:
ama: Bajaj S, Bagley JA, Sommer CM, et al. Neurotransmitter signaling regulates
distinct phases of multimodal human interneuron migration. EMBO Journal.
2021;40(23). doi:10.15252/embj.2021108714
apa: Bajaj, S., Bagley, J. A., Sommer, C. M., Vertesy, A., Nagumo Wong, S., Krenn,
V., … Knoblich, J. A. (2021). Neurotransmitter signaling regulates distinct phases
of multimodal human interneuron migration. EMBO Journal. Embo Press. https://doi.org/10.15252/embj.2021108714
chicago: Bajaj, Sunanjay, Joshua A. Bagley, Christoph M Sommer, Abel Vertesy, Sakurako
Nagumo Wong, Veronica Krenn, Julie Lévi-Strauss, and Juergen A. Knoblich. “Neurotransmitter
Signaling Regulates Distinct Phases of Multimodal Human Interneuron Migration.”
EMBO Journal. Embo Press, 2021. https://doi.org/10.15252/embj.2021108714.
ieee: S. Bajaj et al., “Neurotransmitter signaling regulates distinct phases
of multimodal human interneuron migration,” EMBO Journal, vol. 40, no.
23. Embo Press, 2021.
ista: Bajaj S, Bagley JA, Sommer CM, Vertesy A, Nagumo Wong S, Krenn V, Lévi-Strauss
J, Knoblich JA. 2021. Neurotransmitter signaling regulates distinct phases of
multimodal human interneuron migration. EMBO Journal. 40(23), e108714.
mla: Bajaj, Sunanjay, et al. “Neurotransmitter Signaling Regulates Distinct Phases
of Multimodal Human Interneuron Migration.” EMBO Journal, vol. 40, no.
23, e108714, Embo Press, 2021, doi:10.15252/embj.2021108714.
short: S. Bajaj, J.A. Bagley, C.M. Sommer, A. Vertesy, S. Nagumo Wong, V. Krenn,
J. Lévi-Strauss, J.A. Knoblich, EMBO Journal 40 (2021).
date_created: 2021-10-24T22:01:34Z
date_published: 2021-10-18T00:00:00Z
date_updated: 2023-08-14T08:05:23Z
day: '18'
ddc:
- '610'
department:
- _id: Bio
doi: 10.15252/embj.2021108714
external_id:
isi:
- '000708012800001'
pmid:
- '34661293'
file:
- access_level: open_access
checksum: 78d2d02e775322297e774f72810a41a4
content_type: application/pdf
creator: alisjak
date_created: 2021-12-13T14:54:14Z
date_updated: 2021-12-13T14:54:14Z
file_id: '10541'
file_name: 2021_EMBO_Bajaj.pdf
file_size: 7819881
relation: main_file
success: 1
file_date_updated: 2021-12-13T14:54:14Z
has_accepted_license: '1'
intvolume: ' 40'
isi: 1
issue: '23'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
publication: EMBO Journal
publication_identifier:
eissn:
- 1460-2075
issn:
- 0261-4189
publication_status: published
publisher: Embo Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Neurotransmitter signaling regulates distinct phases of multimodal human interneuron
migration
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: 40
year: '2021'
...
---
_id: '10180'
abstract:
- lang: eng
text: The growing energy and performance costs of deep learning have driven the
community to reduce the size of neural networks by selectively pruning components.
Similarly to their biological counterparts, sparse networks generalize just as
well, sometimes even better than, the original dense networks. Sparsity promises
to reduce the memory footprint of regular networks to fit mobile devices, as well
as shorten training time for ever growing networks. In this paper, we survey prior
work on sparsity in deep learning and provide an extensive tutorial of sparsification
for both inference and training. We describe approaches to remove and add elements
of neural networks, different training strategies to achieve model sparsity, and
mechanisms to exploit sparsity in practice. Our work distills ideas from more
than 300 research papers and provides guidance to practitioners who wish to utilize
sparsity today, as well as to researchers whose goal is to push the frontier forward.
We include the necessary background on mathematical methods in sparsification,
describe phenomena such as early structure adaptation, the intricate relations
between sparsity and the training process, and show techniques for achieving acceleration
on real hardware. We also define a metric of pruned parameter efficiency that
could serve as a baseline for comparison of different sparse networks. We close
by speculating on how sparsity can improve future workloads and outline major
open problems in the field.
acknowledgement: "We thank Doug Burger, Steve Scott, Marco Heddes, and the respective
teams at Microsoft for inspiring discussions on the topic. We thank Angelika Steger
for uplifting debates about the connections to biological brains, Sidak Pal Singh
for his support regarding experimental results, and Utku Evci as well as Xin Wang
for comments on previous versions of this\r\nwork. Special thanks go to Bernhard
Schölkopf, our JMLR editor Samy Bengio, and the three anonymous reviewers who provided
excellent comprehensive, pointed, and deep review comments that improved the quality
of our manuscript significantly."
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Torsten
full_name: Hoefler, Torsten
last_name: Hoefler
- first_name: Dan-Adrian
full_name: Alistarh, Dan-Adrian
id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
last_name: Alistarh
orcid: 0000-0003-3650-940X
- first_name: Tal
full_name: Ben-Nun, Tal
last_name: Ben-Nun
- first_name: Nikoli
full_name: Dryden, Nikoli
last_name: Dryden
- first_name: Elena-Alexandra
full_name: Peste, Elena-Alexandra
id: 32D78294-F248-11E8-B48F-1D18A9856A87
last_name: Peste
citation:
ama: 'Hoefler T, Alistarh D-A, Ben-Nun T, Dryden N, Peste E-A. Sparsity in deep
learning: Pruning and growth for efficient inference and training in neural networks.
Journal of Machine Learning Research. 2021;22(241):1-124.'
apa: 'Hoefler, T., Alistarh, D.-A., Ben-Nun, T., Dryden, N., & Peste, E.-A.
(2021). Sparsity in deep learning: Pruning and growth for efficient inference
and training in neural networks. Journal of Machine Learning Research.
Journal of Machine Learning Research.'
chicago: 'Hoefler, Torsten, Dan-Adrian Alistarh, Tal Ben-Nun, Nikoli Dryden, and
Elena-Alexandra Peste. “Sparsity in Deep Learning: Pruning and Growth for Efficient
Inference and Training in Neural Networks.” Journal of Machine Learning Research.
Journal of Machine Learning Research, 2021.'
ieee: 'T. Hoefler, D.-A. Alistarh, T. Ben-Nun, N. Dryden, and E.-A. Peste, “Sparsity
in deep learning: Pruning and growth for efficient inference and training in neural
networks,” Journal of Machine Learning Research, vol. 22, no. 241. Journal
of Machine Learning Research, pp. 1–124, 2021.'
ista: 'Hoefler T, Alistarh D-A, Ben-Nun T, Dryden N, Peste E-A. 2021. Sparsity in
deep learning: Pruning and growth for efficient inference and training in neural
networks. Journal of Machine Learning Research. 22(241), 1–124.'
mla: 'Hoefler, Torsten, et al. “Sparsity in Deep Learning: Pruning and Growth for
Efficient Inference and Training in Neural Networks.” Journal of Machine Learning
Research, vol. 22, no. 241, Journal of Machine Learning Research, 2021, pp.
1–124.'
short: T. Hoefler, D.-A. Alistarh, T. Ben-Nun, N. Dryden, E.-A. Peste, Journal of
Machine Learning Research 22 (2021) 1–124.
date_created: 2021-10-24T22:01:34Z
date_published: 2021-09-01T00:00:00Z
date_updated: 2022-05-13T09:36:08Z
day: '01'
ddc:
- '000'
department:
- _id: DaAl
external_id:
arxiv:
- '2102.00554'
file:
- access_level: open_access
checksum: 3389d9d01fc58f8fb4c1a53e14a8abbf
content_type: application/pdf
creator: cziletti
date_created: 2021-10-27T15:34:18Z
date_updated: 2021-10-27T15:34:18Z
file_id: '10192'
file_name: 2021_JMachLearnRes_Hoefler.pdf
file_size: 3527521
relation: main_file
success: 1
file_date_updated: 2021-10-27T15:34:18Z
has_accepted_license: '1'
intvolume: ' 22'
issue: '241'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.jmlr.org/papers/v22/21-0366.html
month: '09'
oa: 1
oa_version: Published Version
page: 1-124
publication: Journal of Machine Learning Research
publication_identifier:
eissn:
- 1533-7928
issn:
- 1532-4435
publication_status: published
publisher: Journal of Machine Learning Research
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Sparsity in deep learning: Pruning and growth for efficient inference and
training in neural networks'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 22
year: '2021'
...