---
_id: '3094'
abstract:
- lang: eng
  text: Summary Gravitropism aligns plant growth with gravity. It involves gravity
    perception and the asymmetric distribution of the phytohormone auxin. Here we
    provide insights into the mechanism for hypocotyl gravitropic growth. We show
    that the Arabidopsis thaliana PIN3 auxin transporter is required for the asymmetric
    auxin distribution for the gravitropic response. Gravistimulation polarizes PIN3
    to the bottom side of hypocotyl endodermal cells, which correlates with an increased
    auxin response at the lower hypocotyl side. Both PIN3 polarization and hypocotyl
    bending require the activity of the trafficking regulator GNOM and the protein
    kinase PINOID. Our data suggest that gravity-induced PIN3 polarization diverts
    the auxin flow to mediate the asymmetric distribution of auxin for gravitropic
    shoot bending.
author:
- first_name: Hana
  full_name: Rakusová, Hana
  last_name: Rakusová
- first_name: Javier
  full_name: Gallego-Bartolomé, Javier
  last_name: Gallego Bartolomé
- first_name: Marleen
  full_name: Vanstraelen, Marleen
  last_name: Vanstraelen
- first_name: Hélène
  full_name: Robert, Hélène S
  last_name: Robert
- first_name: David
  full_name: Alabadí, David
  last_name: Alabadí
- first_name: Miguel
  full_name: Blázquez, Miguel A
  last_name: Blázquez
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Rakusová H, Gallego Bartolomé J, Vanstraelen M, et al. Polarization of PIN3
    dependent auxin transport for hypocotyl gravitropic response in Arabidopsis thaliana.
    <i>Plant Journal</i>. 2011;67(5):817-826. doi:<a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">10.1111/j.1365-313X.2011.04636.x</a>
  apa: Rakusová, H., Gallego Bartolomé, J., Vanstraelen, M., Robert, H., Alabadí,
    D., Blázquez, M., … Friml, J. (2011). Polarization of PIN3 dependent auxin transport
    for hypocotyl gravitropic response in Arabidopsis thaliana. <i>Plant Journal</i>.
    Wiley-Blackwell. <a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">https://doi.org/10.1111/j.1365-313X.2011.04636.x</a>
  chicago: Rakusová, Hana, Javier Gallego Bartolomé, Marleen Vanstraelen, Hélène Robert,
    David Alabadí, Miguel Blázquez, Eva Benková, and Jiří Friml. “Polarization of
    PIN3 Dependent Auxin Transport for Hypocotyl Gravitropic Response in Arabidopsis
    Thaliana.” <i>Plant Journal</i>. Wiley-Blackwell, 2011. <a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">https://doi.org/10.1111/j.1365-313X.2011.04636.x</a>.
  ieee: H. Rakusová <i>et al.</i>, “Polarization of PIN3 dependent auxin transport
    for hypocotyl gravitropic response in Arabidopsis thaliana,” <i>Plant Journal</i>,
    vol. 67, no. 5. Wiley-Blackwell, pp. 817–826, 2011.
  ista: Rakusová H, Gallego Bartolomé J, Vanstraelen M, Robert H, Alabadí D, Blázquez
    M, Benková E, Friml J. 2011. Polarization of PIN3 dependent auxin transport for
    hypocotyl gravitropic response in Arabidopsis thaliana. Plant Journal. 67(5),
    817–826.
  mla: Rakusová, Hana, et al. “Polarization of PIN3 Dependent Auxin Transport for
    Hypocotyl Gravitropic Response in Arabidopsis Thaliana.” <i>Plant Journal</i>,
    vol. 67, no. 5, Wiley-Blackwell, 2011, pp. 817–26, doi:<a href="https://doi.org/10.1111/j.1365-313X.2011.04636.x">10.1111/j.1365-313X.2011.04636.x</a>.
  short: H. Rakusová, J. Gallego Bartolomé, M. Vanstraelen, H. Robert, D. Alabadí,
    M. Blázquez, E. Benková, J. Friml, Plant Journal 67 (2011) 817–826.
date_created: 2018-12-11T12:01:21Z
date_published: 2011-09-01T00:00:00Z
date_updated: 2021-01-12T07:41:01Z
day: '01'
doi: 10.1111/j.1365-313X.2011.04636.x
extern: 1
intvolume: '        67'
issue: '5'
month: '09'
page: 817 - 826
publication: Plant Journal
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3606'
quality_controlled: 0
status: public
title: Polarization of PIN3 dependent auxin transport for hypocotyl gravitropic response
  in Arabidopsis thaliana
type: journal_article
volume: 67
year: '2011'
...
---
_id: '3095'
abstract:
- lang: eng
  text: Root system architecture depends on lateral root (LR) initiation that takes
    place in a relatively narrow developmental window (DW). Here, we analyzed the
    role of auxin gradients established along the parent root in defining this DW
    for LR initiation. Correlations between auxin distribution and response, and spatiotemporal
    control of LR initiation were analyzed in Arabidopsis thaliana and tomato (Solanum
    lycopersicum). In both Arabidopsis and tomato roots, a well defined zone, where
    auxin content and response are minimal, demarcates the position of a DW for founder
    cell specification and LR initiation. We show that in the zone of auxin minimum
    pericycle cells have highest probability to become founder cells and that auxin
    perception via the TIR1/AFB pathway, and polar auxin transport, are essential
    for the establishment of this zone. Altogether, this study reveals that the same
    morphogen-like molecule, auxin, can act simultaneously as a morphogenetic trigger
    of LR founder cell identity and as a gradient-dependent signal defining positioning
    of the founder cell specification. This auxin minimum zone might represent an
    important control mechanism ensuring the LR initiation steadiness and the acropetal
    LR initiation pattern. © 2011 The Authors. New Phytologist © 2011 New Phytologist
    Trust.
author:
- first_name: Joseph
  full_name: Dubrovsky, Joseph G
  last_name: Dubrovsky
- first_name: Selene
  full_name: Napsucialy-Mendivil, Selene
  last_name: Napsucialy Mendivil
- first_name: Jérôme
  full_name: Duclercq, Jérôme
  last_name: Duclercq
- first_name: Yan
  full_name: Cheng, Yan
  last_name: Cheng
- first_name: Svetlana
  full_name: Shishkova, Svetlana O
  last_name: Shishkova
- first_name: Maria
  full_name: Ivanchenko, Maria G
  last_name: Ivanchenko
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Angus
  full_name: Murphy, Angus S
  last_name: Murphy
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
citation:
  ama: Dubrovsky J, Napsucialy Mendivil S, Duclercq J, et al. Auxin minimum defines
    a developmental window for lateral root initiation. <i>New Phytologist</i>. 2011;191(4):970-983.
    doi:<a href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x"> 10.1111/j.1469-8137.2011.03757.x</a>
  apa: Dubrovsky, J., Napsucialy Mendivil, S., Duclercq, J., Cheng, Y., Shishkova,
    S., Ivanchenko, M., … Benková, E. (2011). Auxin minimum defines a developmental
    window for lateral root initiation. <i>New Phytologist</i>. Wiley-Blackwell. <a
    href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x">https://doi.org/ 10.1111/j.1469-8137.2011.03757.x</a>
  chicago: Dubrovsky, Joseph, Selene Napsucialy Mendivil, Jérôme Duclercq, Yan Cheng,
    Svetlana Shishkova, Maria Ivanchenko, Jiří Friml, Angus Murphy, and Eva Benková.
    “Auxin Minimum Defines a Developmental Window for Lateral Root Initiation.” <i>New
    Phytologist</i>. Wiley-Blackwell, 2011. <a href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x">https://doi.org/
    10.1111/j.1469-8137.2011.03757.x</a>.
  ieee: J. Dubrovsky <i>et al.</i>, “Auxin minimum defines a developmental window
    for lateral root initiation,” <i>New Phytologist</i>, vol. 191, no. 4. Wiley-Blackwell,
    pp. 970–983, 2011.
  ista: Dubrovsky J, Napsucialy Mendivil S, Duclercq J, Cheng Y, Shishkova S, Ivanchenko
    M, Friml J, Murphy A, Benková E. 2011. Auxin minimum defines a developmental window
    for lateral root initiation. New Phytologist. 191(4), 970–983.
  mla: Dubrovsky, Joseph, et al. “Auxin Minimum Defines a Developmental Window for
    Lateral Root Initiation.” <i>New Phytologist</i>, vol. 191, no. 4, Wiley-Blackwell,
    2011, pp. 970–83, doi:<a href="https://doi.org/ 10.1111/j.1469-8137.2011.03757.x">
    10.1111/j.1469-8137.2011.03757.x</a>.
  short: J. Dubrovsky, S. Napsucialy Mendivil, J. Duclercq, Y. Cheng, S. Shishkova,
    M. Ivanchenko, J. Friml, A. Murphy, E. Benková, New Phytologist 191 (2011) 970–983.
date_created: 2018-12-11T12:01:21Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2021-01-12T07:41:01Z
day: '01'
doi: ' 10.1111/j.1469-8137.2011.03757.x'
extern: 1
intvolume: '       191'
issue: '4'
month: '01'
page: 970 - 983
publication: New Phytologist
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3605'
quality_controlled: 0
status: public
title: Auxin minimum defines a developmental window for lateral root initiation
type: journal_article
volume: 191
year: '2011'
...
---
_id: '3096'
abstract:
- lang: eng
  text: Carrier-dependent, intercellular auxin transport is central to the developmental
    patterning of higher plants (tracheophytes). The evolution of this polar auxin
    transport might be linked to the translocation of some PIN auxin efflux carriers
    from their presumably ancestral localization at the endoplasmic reticulum (ER)
    to the polar domains at the plasma membrane. Here we propose an eventually ancient
    mechanism of intercellular auxin distribution by ER-localized auxin transporters
    involving intracellular auxin retention and switch-like release from the ER. The
    proposed model integrates feedback circuits utilizing the conserved nuclear auxin
    signaling for the regulation of PIN transcription and a hypothetical ER-based
    signaling for the regulation of PIN-dependent transport activity at the ER. Computer
    simulations of the model revealed its plausibility for generating auxin channels
    and localized auxin maxima highlighting the possibility of this alternative mechanism
    for polar auxin transport.
author:
- first_name: Krzysztof T
  full_name: Wabnik, Krzysztof T
  id: 4DE369A4-F248-11E8-B48F-1D18A9856A87
  last_name: Wabnik
  orcid: 0000-0001-7263-0560
- first_name: Jürgen
  full_name: Kleine Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Willy
  full_name: Govaerts, Willy
  last_name: Govaerts
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Wabnik KT, Kleine Vehn J, Govaerts W, Friml J. Prototype cell-to-cell auxin
    transport mechanism by intracellular auxin compartmentalization. <i>Trends in
    Plant Science</i>. 2011;16(9):468-475. doi:<a href="https://doi.org/10.1016/j.tplants.2011.05.002">10.1016/j.tplants.2011.05.002</a>
  apa: Wabnik, K. T., Kleine Vehn, J., Govaerts, W., &#38; Friml, J. (2011). Prototype
    cell-to-cell auxin transport mechanism by intracellular auxin compartmentalization.
    <i>Trends in Plant Science</i>. Cell Press. <a href="https://doi.org/10.1016/j.tplants.2011.05.002">https://doi.org/10.1016/j.tplants.2011.05.002</a>
  chicago: Wabnik, Krzysztof T, Jürgen Kleine Vehn, Willy Govaerts, and Jiří Friml.
    “Prototype Cell-to-Cell Auxin Transport Mechanism by Intracellular Auxin Compartmentalization.”
    <i>Trends in Plant Science</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.tplants.2011.05.002">https://doi.org/10.1016/j.tplants.2011.05.002</a>.
  ieee: K. T. Wabnik, J. Kleine Vehn, W. Govaerts, and J. Friml, “Prototype cell-to-cell
    auxin transport mechanism by intracellular auxin compartmentalization,” <i>Trends
    in Plant Science</i>, vol. 16, no. 9. Cell Press, pp. 468–475, 2011.
  ista: Wabnik KT, Kleine Vehn J, Govaerts W, Friml J. 2011. Prototype cell-to-cell
    auxin transport mechanism by intracellular auxin compartmentalization. Trends
    in Plant Science. 16(9), 468–475.
  mla: Wabnik, Krzysztof T., et al. “Prototype Cell-to-Cell Auxin Transport Mechanism
    by Intracellular Auxin Compartmentalization.” <i>Trends in Plant Science</i>,
    vol. 16, no. 9, Cell Press, 2011, pp. 468–75, doi:<a href="https://doi.org/10.1016/j.tplants.2011.05.002">10.1016/j.tplants.2011.05.002</a>.
  short: K.T. Wabnik, J. Kleine Vehn, W. Govaerts, J. Friml, Trends in Plant Science
    16 (2011) 468–475.
date_created: 2018-12-11T12:01:21Z
date_published: 2011-09-01T00:00:00Z
date_updated: 2021-01-12T07:41:01Z
day: '01'
doi: 10.1016/j.tplants.2011.05.002
extern: '1'
intvolume: '        16'
issue: '9'
language:
- iso: eng
month: '09'
oa_version: None
page: 468 - 475
publication: Trends in Plant Science
publication_status: published
publisher: Cell Press
publist_id: '3604'
quality_controlled: '1'
status: public
title: Prototype cell-to-cell auxin transport mechanism by intracellular auxin compartmentalization
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2011'
...
---
_id: '3097'
abstract:
- lang: eng
  text: Cytokinin is an important regulator of plant growth and development. In Arabidopsis
    thaliana, the two-component phosphorelay mediated through a family of histidine
    kinases and response regulators is recognized as the principal cytokinin signal
    transduction mechanism activating the complex transcriptional response to control
    various developmental processes. Here, we identified an alternative mode of cytokinin
    action that uses endocytic trafficking as a means to direct plant organogenesis.
    This activity occurs downstream of known cytokinin receptors but through a branch
    of the cytokinin signaling pathway that does not involve transcriptional regulation.
    We show that cytokinin regulates endocytic recycling of the auxin efflux carrier
    PINFORMED1 (PIN1) by redirecting it for lytic degradation in vacuoles. Stimulation
    of the lytic PIN1 degradation is not a default effect for general downregulation
    of proteins from plasma membranes, but a specific mechanism to rapidly modulate
    the auxin distribution in cytokinin-mediated developmental processes.
author:
- first_name: Peter
  full_name: Peter Marhavy
  id: 3F45B078-F248-11E8-B48F-1D18A9856A87
  last_name: Marhavy
  orcid: 0000-0001-5227-5741
- first_name: Agnieszka
  full_name: Bielach, Agnieszka
  last_name: Bielach
- first_name: Lindy
  full_name: Abas, Lindy
  last_name: Abas
- first_name: Anas
  full_name: Abuzeineh, Anas
  last_name: Abuzeineh
- first_name: Jérôme
  full_name: Duclercq, Jérôme
  last_name: Duclercq
- first_name: Hirokazu
  full_name: Tanaka, Hirokazu
  last_name: Tanaka
- first_name: Markéta
  full_name: Pařezová, Markéta
  last_name: Pařezová
- first_name: Jan
  full_name: Petrášek, Jan
  last_name: Petrášek
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
citation:
  ama: Marhavý P, Bielach A, Abas L, et al. Cytokinin modulates endocytic trafficking
    of PIN1 auxin efflux carrier to control plant organogenesis. <i>Developmental
    Cell</i>. 2011;21(4):796-804. doi:<a href="https://doi.org/10.1016/j.devcel.2011.08.014">10.1016/j.devcel.2011.08.014</a>
  apa: Marhavý, P., Bielach, A., Abas, L., Abuzeineh, A., Duclercq, J., Tanaka, H.,
    … Benková, E. (2011). Cytokinin modulates endocytic trafficking of PIN1 auxin
    efflux carrier to control plant organogenesis. <i>Developmental Cell</i>. Cell
    Press. <a href="https://doi.org/10.1016/j.devcel.2011.08.014">https://doi.org/10.1016/j.devcel.2011.08.014</a>
  chicago: Marhavý, Peter, Agnieszka Bielach, Lindy Abas, Anas Abuzeineh, Jérôme Duclercq,
    Hirokazu Tanaka, Markéta Pařezová, et al. “Cytokinin Modulates Endocytic Trafficking
    of PIN1 Auxin Efflux Carrier to Control Plant Organogenesis.” <i>Developmental
    Cell</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.devcel.2011.08.014">https://doi.org/10.1016/j.devcel.2011.08.014</a>.
  ieee: P. Marhavý <i>et al.</i>, “Cytokinin modulates endocytic trafficking of PIN1
    auxin efflux carrier to control plant organogenesis,” <i>Developmental Cell</i>,
    vol. 21, no. 4. Cell Press, pp. 796–804, 2011.
  ista: Marhavý P, Bielach A, Abas L, Abuzeineh A, Duclercq J, Tanaka H, Pařezová
    M, Petrášek J, Friml J, Kleine Vehn J, Benková E. 2011. Cytokinin modulates endocytic
    trafficking of PIN1 auxin efflux carrier to control plant organogenesis. Developmental
    Cell. 21(4), 796–804.
  mla: Marhavý, Peter, et al. “Cytokinin Modulates Endocytic Trafficking of PIN1 Auxin
    Efflux Carrier to Control Plant Organogenesis.” <i>Developmental Cell</i>, vol.
    21, no. 4, Cell Press, 2011, pp. 796–804, doi:<a href="https://doi.org/10.1016/j.devcel.2011.08.014">10.1016/j.devcel.2011.08.014</a>.
  short: P. Marhavý, A. Bielach, L. Abas, A. Abuzeineh, J. Duclercq, H. Tanaka, M.
    Pařezová, J. Petrášek, J. Friml, J. Kleine Vehn, E. Benková, Developmental Cell
    21 (2011) 796–804.
date_created: 2018-12-11T12:01:22Z
date_published: 2011-10-18T00:00:00Z
date_updated: 2021-01-12T07:41:02Z
day: '18'
doi: 10.1016/j.devcel.2011.08.014
extern: 1
intvolume: '        21'
issue: '4'
month: '10'
page: 796 - 804
publication: Developmental Cell
publication_status: published
publisher: Cell Press
publist_id: '3603'
quality_controlled: 0
status: public
title: Cytokinin modulates endocytic trafficking of PIN1 auxin efflux carrier to control
  plant organogenesis
type: journal_article
volume: 21
year: '2011'
...
---
_id: '3098'
abstract:
- lang: eng
  text: Cell polarity reflected by asymmetric distribution of proteins at the plasma
    membrane is a fundamental feature of unicellular and multicellular organisms.
    It remains conceptually unclear how cell polarity is kept in cell wall-encapsulated
    plant cells. We have used super-resolution and semi-quantitative live-cell imaging
    in combination with pharmacological, genetic, and computational approaches to
    reveal insights into the mechanism of cell polarity maintenance in Arabidopsis
    thaliana. We show that polar-competent PIN transporters for the phytohormone auxin
    are delivered to the center of polar domains by super-polar recycling. Within
    the plasma membrane, PINs are recruited into non-mobile membrane clusters and
    their lateral diffusion is dramatically reduced, which ensures longer polar retention.
    At the circumventing edges of the polar domain, spatially defined internalization
    of escaped cargos occurs by clathrin-dependent endocytosis. Computer simulations
    confirm that the combination of these processes provides a robust mechanism for
    polarity maintenance in plant cells. Moreover, our study suggests that the regulation
    of lateral diffusion and spatially defined endocytosis, but not super-polar exocytosis
    have primary importance for PIN polarity maintenance.
author:
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Krzysztof T
  full_name: Krzysztof Wabnik
  id: 4DE369A4-F248-11E8-B48F-1D18A9856A87
  last_name: Wabnik
  orcid: 0000-0001-7263-0560
- first_name: Alexandre
  full_name: Martinière, Alexandre
  last_name: Martinière
- first_name: Łukasz
  full_name: Łangowski, Łukasz
  last_name: Łangowski
- first_name: Katrin
  full_name: Willig, Katrin
  last_name: Willig
- first_name: Satoshi
  full_name: Naramoto, Satoshi
  last_name: Naramoto
- first_name: Johannes
  full_name: Leitner, Johannes
  last_name: Leitner
- first_name: Hirokazu
  full_name: Tanaka, Hirokazu
  last_name: Tanaka
- first_name: Stefan
  full_name: Jakobs, Stefan
  last_name: Jakobs
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
- first_name: Christian
  full_name: Luschnig, Christian
  last_name: Luschnig
- first_name: Willy
  full_name: Govaerts, Willy J
  last_name: Govaerts
- first_name: Stefan
  full_name: Hell, Stefan W
  last_name: Hell
- first_name: John
  full_name: Runions, John
  last_name: Runions
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Kleine Vehn J, Wabnik KT, Martinière A, et al. Recycling, clustering and endocytosis
    jointly maintain PIN auxin carrier polarity at the plasma membrane. <i>Molecular
    Systems Biology</i>. 2011;7. doi:<a href="https://doi.org/10.1038/msb.2011.72">10.1038/msb.2011.72</a>
  apa: Kleine Vehn, J., Wabnik, K. T., Martinière, A., Łangowski, Ł., Willig, K.,
    Naramoto, S., … Friml, J. (2011). Recycling, clustering and endocytosis jointly
    maintain PIN auxin carrier polarity at the plasma membrane. <i>Molecular Systems
    Biology</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/msb.2011.72">https://doi.org/10.1038/msb.2011.72</a>
  chicago: Kleine Vehn, Jürgen, Krzysztof T Wabnik, Alexandre Martinière, Łukasz Łangowski,
    Katrin Willig, Satoshi Naramoto, Johannes Leitner, et al. “Recycling, Clustering
    and Endocytosis Jointly Maintain PIN Auxin Carrier Polarity at the Plasma Membrane.”
    <i>Molecular Systems Biology</i>. Nature Publishing Group, 2011. <a href="https://doi.org/10.1038/msb.2011.72">https://doi.org/10.1038/msb.2011.72</a>.
  ieee: J. Kleine Vehn <i>et al.</i>, “Recycling, clustering and endocytosis jointly
    maintain PIN auxin carrier polarity at the plasma membrane,” <i>Molecular Systems
    Biology</i>, vol. 7. Nature Publishing Group, 2011.
  ista: Kleine Vehn J, Wabnik KT, Martinière A, Łangowski Ł, Willig K, Naramoto S,
    Leitner J, Tanaka H, Jakobs S, Robert S, Luschnig C, Govaerts W, Hell S, Runions
    J, Friml J. 2011. Recycling, clustering and endocytosis jointly maintain PIN auxin
    carrier polarity at the plasma membrane. Molecular Systems Biology. 7.
  mla: Kleine Vehn, Jürgen, et al. “Recycling, Clustering and Endocytosis Jointly
    Maintain PIN Auxin Carrier Polarity at the Plasma Membrane.” <i>Molecular Systems
    Biology</i>, vol. 7, Nature Publishing Group, 2011, doi:<a href="https://doi.org/10.1038/msb.2011.72">10.1038/msb.2011.72</a>.
  short: J. Kleine Vehn, K.T. Wabnik, A. Martinière, Ł. Łangowski, K. Willig, S. Naramoto,
    J. Leitner, H. Tanaka, S. Jakobs, S. Robert, C. Luschnig, W. Govaerts, S. Hell,
    J. Runions, J. Friml, Molecular Systems Biology 7 (2011).
date_created: 2018-12-11T12:01:22Z
date_published: 2011-10-25T00:00:00Z
date_updated: 2021-01-12T07:41:02Z
day: '25'
doi: 10.1038/msb.2011.72
extern: 1
intvolume: '         7'
month: '10'
publication: Molecular Systems Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '3601'
quality_controlled: 0
status: public
title: Recycling, clustering and endocytosis jointly maintain PIN auxin carrier polarity
  at the plasma membrane
type: journal_article
volume: 7
year: '2011'
...
---
_id: '3099'
abstract:
- lang: eng
  text: Endomembrane trafficking relies on the coordination of a highly complex, dynamic
    network of intracellular vesicles. Understanding the network will require a dissection
    of cargo and vesicle dynamics at the cellular level in vivo. This is also a key
    to establishing a link between vesicular networks and their functional roles in
    development. We used a high-content intracellular screen to discover small molecules
    targeting endomembrane trafficking in vivo in a complex eukaryote, Arabidopsis
    thaliana. Tens of thousands of molecules were prescreened and a selected subset
    was interrogated against a panel of plasma membrane (PM) and other endomembrane
    compartment markers to identify molecules that altered vesicle trafficking. The
    extensive image dataset was transformed by a flexible algorithm into a marker-by-phenotype-by-treatment
    time matrix and revealed groups of molecules that induced similar subcellular
    fingerprints (clusters). This matrix provides a platform for a systems view of
    trafficking. Molecules from distinct clusters presented avenues and enabled an
    entry point to dissect recycling at the PM, vacuolar sorting, and cell-plate maturation.
    Bioactivity in human cells indicated the value of the approach to identifying
    small molecules that are active in diverse organisms for biology and drug discovery.
author:
- first_name: Georgia
  full_name: Drakakaki, Georgia
  last_name: Drakakaki
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
- first_name: Anna
  full_name: Szatmári, Anna-Maria
  last_name: Szatmári
- first_name: Michelle
  full_name: Brown, Michelle Q
  last_name: Brown
- first_name: Shingo
  full_name: Nagawa, Shingo
  last_name: Nagawa
- first_name: Daniël
  full_name: Van Damme, Daniël
  last_name: Van Damme
- first_name: Marylin
  full_name: Leonard, Marylin
  last_name: Leonard
- first_name: Zhenbiao
  full_name: Yang, Zhenbiao
  last_name: Yang
- first_name: Thomas
  full_name: Girke, Thomas
  last_name: Girke
- first_name: Sandra
  full_name: Schmid, Sandra L
  last_name: Schmid
- first_name: Eugenia
  full_name: Russinova, Eugenia
  last_name: Russinova
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Natasha
  full_name: Raikhel, Natasha V
  last_name: Raikhel
- first_name: Glen
  full_name: Hicks, Glen R
  last_name: Hicks
citation:
  ama: Drakakaki G, Robert S, Szatmári A, et al. Clusters of bioactive compounds target
    dynamic endomembrane networks in vivo. <i>PNAS</i>. 2011;108(43):17850-17855.
    doi:<a href="https://doi.org/10.1073/pnas.1108581108">10.1073/pnas.1108581108</a>
  apa: Drakakaki, G., Robert, S., Szatmári, A., Brown, M., Nagawa, S., Van Damme,
    D., … Hicks, G. (2011). Clusters of bioactive compounds target dynamic endomembrane
    networks in vivo. <i>PNAS</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1108581108">https://doi.org/10.1073/pnas.1108581108</a>
  chicago: Drakakaki, Georgia, Stéphanie Robert, Anna Szatmári, Michelle Brown, Shingo
    Nagawa, Daniël Van Damme, Marylin Leonard, et al. “Clusters of Bioactive Compounds
    Target Dynamic Endomembrane Networks in Vivo.” <i>PNAS</i>. National Academy of
    Sciences, 2011. <a href="https://doi.org/10.1073/pnas.1108581108">https://doi.org/10.1073/pnas.1108581108</a>.
  ieee: G. Drakakaki <i>et al.</i>, “Clusters of bioactive compounds target dynamic
    endomembrane networks in vivo,” <i>PNAS</i>, vol. 108, no. 43. National Academy
    of Sciences, pp. 17850–17855, 2011.
  ista: Drakakaki G, Robert S, Szatmári A, Brown M, Nagawa S, Van Damme D, Leonard
    M, Yang Z, Girke T, Schmid S, Russinova E, Friml J, Raikhel N, Hicks G. 2011.
    Clusters of bioactive compounds target dynamic endomembrane networks in vivo.
    PNAS. 108(43), 17850–17855.
  mla: Drakakaki, Georgia, et al. “Clusters of Bioactive Compounds Target Dynamic
    Endomembrane Networks in Vivo.” <i>PNAS</i>, vol. 108, no. 43, National Academy
    of Sciences, 2011, pp. 17850–55, doi:<a href="https://doi.org/10.1073/pnas.1108581108">10.1073/pnas.1108581108</a>.
  short: G. Drakakaki, S. Robert, A. Szatmári, M. Brown, S. Nagawa, D. Van Damme,
    M. Leonard, Z. Yang, T. Girke, S. Schmid, E. Russinova, J. Friml, N. Raikhel,
    G. Hicks, PNAS 108 (2011) 17850–17855.
date_created: 2018-12-11T12:01:23Z
date_published: 2011-10-25T00:00:00Z
date_updated: 2021-01-12T07:41:02Z
day: '25'
doi: 10.1073/pnas.1108581108
extern: 1
intvolume: '       108'
issue: '43'
month: '10'
page: 17850 - 17855
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3602'
quality_controlled: 0
status: public
title: Clusters of bioactive compounds target dynamic endomembrane networks in vivo
type: journal_article
volume: 108
year: '2011'
...
---
_id: '3100'
abstract:
- lang: eng
  text: In multicellular organisms, morphogenesis relies on a strict coordination
    in time and space of cell proliferation and differentiation. In contrast to animals,
    plant development displays continuous organ formation and adaptive growth responses
    during their lifespan relying on a tight coordination of cell proliferation. How
    developmental signals interact with the plant cell-cycle machinery is largely
    unknown. Here, we characterize plant A2-type cyclins, a small gene family of mitotic
    cyclins, and show how they contribute to the fine-tuning of local proliferation
    during plant development. Moreover, the timely repression of CYCA2;3 expression
    in newly formed guard cells is shown to require the stomatal transcription factors
    FOUR LIPS/MYB124 and MYB88, providing a direct link between developmental programming
    and cell-cycle exit in plants. Thus, transcriptional downregulation of CYCA2s
    represents a critical mechanism to coordinate proliferation during plant development.
author:
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Frederik
  full_name: Coppens, Frederik
  last_name: Coppens
- first_name: Eunkyoung
  full_name: Lee, EunKyoung
  last_name: Lee
- first_name: Tyler
  full_name: Donner, Tyler J
  last_name: Donner
- first_name: Zidian
  full_name: Xie, Zidian
  last_name: Xie
- first_name: Gert
  full_name: Van Isterdael, Gert
  last_name: Van Isterdael
- first_name: Stijn
  full_name: Dhondt, Stijn
  last_name: Dhondt
- first_name: Freya
  full_name: De Winter, Freya
  last_name: De Winter
- first_name: Bert
  full_name: De Rybel, Bert
  last_name: De Rybel
- first_name: Marnik
  full_name: Vuylsteke, Marnik
  last_name: Vuylsteke
- first_name: Lieven
  full_name: De Veylder, Lieven
  last_name: De Veylder
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Dirk
  full_name: Inzé, Dirk
  last_name: Inzé
- first_name: Erich
  full_name: Grotewold, Erich
  last_name: Grotewold
- first_name: Enrico
  full_name: Scarpella, Enrico
  last_name: Scarpella
- first_name: Fred
  full_name: Sack, Fred
  last_name: Sack
- first_name: Gerrit
  full_name: Beemster, Gerrit T
  last_name: Beemster
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
citation:
  ama: Vanneste S, Coppens F, Lee E, et al. Developmental regulation of CYCA2s contributes
    to tissue-specific proliferation in Arabidopsis . <i>EMBO Journal</i>. 2011;30(16):3430-3441.
    doi:<a href="https://doi.org/10.1038/emboj.2011.240">10.1038/emboj.2011.240</a>
  apa: Vanneste, S., Coppens, F., Lee, E., Donner, T., Xie, Z., Van Isterdael, G.,
    … Beeckman, T. (2011). Developmental regulation of CYCA2s contributes to tissue-specific
    proliferation in Arabidopsis . <i>EMBO Journal</i>. Wiley-Blackwell. <a href="https://doi.org/10.1038/emboj.2011.240">https://doi.org/10.1038/emboj.2011.240</a>
  chicago: Vanneste, Steffen, Frederik Coppens, Eunkyoung Lee, Tyler Donner, Zidian
    Xie, Gert Van Isterdael, Stijn Dhondt, et al. “Developmental Regulation of CYCA2s
    Contributes to Tissue-Specific Proliferation in Arabidopsis .” <i>EMBO Journal</i>.
    Wiley-Blackwell, 2011. <a href="https://doi.org/10.1038/emboj.2011.240">https://doi.org/10.1038/emboj.2011.240</a>.
  ieee: S. Vanneste <i>et al.</i>, “Developmental regulation of CYCA2s contributes
    to tissue-specific proliferation in Arabidopsis ,” <i>EMBO Journal</i>, vol. 30,
    no. 16. Wiley-Blackwell, pp. 3430–3441, 2011.
  ista: Vanneste S, Coppens F, Lee E, Donner T, Xie Z, Van Isterdael G, Dhondt S,
    De Winter F, De Rybel B, Vuylsteke M, De Veylder L, Friml J, Inzé D, Grotewold
    E, Scarpella E, Sack F, Beemster G, Beeckman T. 2011. Developmental regulation
    of CYCA2s contributes to tissue-specific proliferation in Arabidopsis . EMBO Journal.
    30(16), 3430–3441.
  mla: Vanneste, Steffen, et al. “Developmental Regulation of CYCA2s Contributes to
    Tissue-Specific Proliferation in Arabidopsis .” <i>EMBO Journal</i>, vol. 30,
    no. 16, Wiley-Blackwell, 2011, pp. 3430–41, doi:<a href="https://doi.org/10.1038/emboj.2011.240">10.1038/emboj.2011.240</a>.
  short: S. Vanneste, F. Coppens, E. Lee, T. Donner, Z. Xie, G. Van Isterdael, S.
    Dhondt, F. De Winter, B. De Rybel, M. Vuylsteke, L. De Veylder, J. Friml, D. Inzé,
    E. Grotewold, E. Scarpella, F. Sack, G. Beemster, T. Beeckman, EMBO Journal 30
    (2011) 3430–3441.
date_created: 2018-12-11T12:01:23Z
date_published: 2011-08-17T00:00:00Z
date_updated: 2021-01-12T07:41:04Z
day: '17'
doi: 10.1038/emboj.2011.240
extern: 1
intvolume: '        30'
issue: '16'
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160660/
month: '08'
oa: 1
page: 3430 - 3441
publication: EMBO Journal
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3600'
quality_controlled: 0
status: public
title: 'Developmental regulation of CYCA2s contributes to tissue-specific proliferation
  in Arabidopsis '
type: journal_article
volume: 30
year: '2011'
...
---
_id: '3101'
abstract:
- lang: eng
  text: Subcellular trafficking is required for a multitude of functions in eukaryotic
    cells. It involves regulation of cargo sorting, vesicle formation, trafficking
    and fusion processes at multiple levels. Adaptor protein (AP) complexes are key
    regulators of cargo sorting into vesicles in yeast and mammals but their existence
    and function in plants have not been demonstrated. Here we report the identification
    of the protein-affected trafficking 4 (pat4) mutant defective in the putative
    δ subunit of the AP-3 complex. pat4 and pat2, a mutant isolated from the same
    GFP imaging-based forward genetic screen that lacks a functional putative AP-3
    β, as well as dominant negative AP-3 μ transgenic lines display undistinguishable
    phenotypes characterized by largely normal morphology and development, but strong
    intracellular accumulation of membrane proteins in aberrant vacuolar structures.
    All mutants are defective in morphology and function of lytic and protein storage
    vacuoles (PSVs) but show normal sorting of reserve proteins to PSVs. Immunoprecipitation
    experiments and genetic studies revealed tight functional and physical associations
    of putative AP-3 β and AP-3 δ subunits. Furthermore, both proteins are closely
    linked with putative AP-3 μ and σ subunits and several components of the clathrin
    and dynamin machineries. Taken together, these results demonstrate that AP complexes,
    similar to those in other eukaryotes, exist in plants, and that AP-3 plays a specific
    role in the regulation of biogenesis and function of vacuoles in plant cells.
    © 2011 IBCB, SIBS, CAS All rights reserved
author:
- first_name: Marta
  full_name: Zwiewka, Marta
  last_name: Zwiewka
- first_name: Elena
  full_name: Feraru, Elena
  last_name: Feraru
- first_name: Barbara
  full_name: Möller, Barbara
  last_name: Möller
- first_name: Inhwan
  full_name: Hwang, Inhwan
  last_name: Hwang
- first_name: Mugurel
  full_name: Feraru, Mugurel I
  last_name: Feraru
- first_name: Jürgen
  full_name: Kleine-Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Zwiewka M, Feraru E, Möller B, et al. The AP 3 adaptor complex is required
    for vacuolar function in Arabidopsis. <i>Cell Research</i>. 2011;21(12):1711-1722.
    doi:<a href="https://doi.org/10.1038/cr.2011.99">10.1038/cr.2011.99</a>
  apa: Zwiewka, M., Feraru, E., Möller, B., Hwang, I., Feraru, M., Kleine Vehn, J.,
    … Friml, J. (2011). The AP 3 adaptor complex is required for vacuolar function
    in Arabidopsis. <i>Cell Research</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/cr.2011.99">https://doi.org/10.1038/cr.2011.99</a>
  chicago: Zwiewka, Marta, Elena Feraru, Barbara Möller, Inhwan Hwang, Mugurel Feraru,
    Jürgen Kleine Vehn, Dolf Weijers, and Jiří Friml. “The AP 3 Adaptor Complex Is
    Required for Vacuolar Function in Arabidopsis.” <i>Cell Research</i>. Nature Publishing
    Group, 2011. <a href="https://doi.org/10.1038/cr.2011.99">https://doi.org/10.1038/cr.2011.99</a>.
  ieee: M. Zwiewka <i>et al.</i>, “The AP 3 adaptor complex is required for vacuolar
    function in Arabidopsis,” <i>Cell Research</i>, vol. 21, no. 12. Nature Publishing
    Group, pp. 1711–1722, 2011.
  ista: Zwiewka M, Feraru E, Möller B, Hwang I, Feraru M, Kleine Vehn J, Weijers D,
    Friml J. 2011. The AP 3 adaptor complex is required for vacuolar function in Arabidopsis.
    Cell Research. 21(12), 1711–1722.
  mla: Zwiewka, Marta, et al. “The AP 3 Adaptor Complex Is Required for Vacuolar Function
    in Arabidopsis.” <i>Cell Research</i>, vol. 21, no. 12, Nature Publishing Group,
    2011, pp. 1711–22, doi:<a href="https://doi.org/10.1038/cr.2011.99">10.1038/cr.2011.99</a>.
  short: M. Zwiewka, E. Feraru, B. Möller, I. Hwang, M. Feraru, J. Kleine Vehn, D.
    Weijers, J. Friml, Cell Research 21 (2011) 1711–1722.
date_created: 2018-12-11T12:01:23Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2021-01-12T07:41:04Z
day: '01'
doi: 10.1038/cr.2011.99
extern: 1
intvolume: '        21'
issue: '12'
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357998/
month: '01'
oa: 1
page: 1711 - 1722
publication: Cell Research
publication_status: published
publisher: Nature Publishing Group
publist_id: '3597'
quality_controlled: 0
status: public
title: The AP 3 adaptor complex is required for vacuolar function in Arabidopsis
type: journal_article
volume: 21
year: '2011'
...
---
_id: '3102'
abstract:
- lang: eng
  text: 'Multicellular organisms depend on cell production, cell fate specification,
    and correct patterning to shape their adult body. In plants, auxin plays a prominent
    role in the timely coordination of these different cellular processes. A well-studied
    example is lateral root initiation, in which auxin triggers founder cell specification
    and cell cycle activation of xylem pole–positioned pericycle cells. Here, we report
    that the E2Fa transcription factor of Arabidopsis thaliana is an essential component
    that regulates the asymmetric cell division marking lateral root initiation. Moreover,
    we demonstrate that E2Fa expression is regulated by the LATERAL ORGAN BOUNDARY
    DOMAIN18/LATERAL ORGAN BOUNDARY DOMAIN33 (LBD18/LBD33) dimer that is, in turn,
    regulated by the auxin signaling pathway. LBD18/LBD33 mediates lateral root organogenesis
    through E2Fa transcriptional activation, whereas E2Fa expression under control
    of the LBD18 promoter eliminates the need for LBD18. Besides lateral root initiation,
    vascular patterning is disrupted in E2Fa knockout plants, similarly as it is affected
    in auxin signaling and lbd mutants, indicating that the transcriptional induction
    of E2Fa through LBDs represents a general mechanism for auxin-dependent cell cycle
    activation. Our data illustrate how a conserved mechanism driving cell cycle entry
    has been adapted evolutionarily to connect auxin signaling with control of processes
    determining plant architecture. '
author:
- first_name: Barbara
  full_name: Berckmans, Barbara
  last_name: Berckmans
- first_name: Valya
  full_name: Vassileva, Valya
  last_name: Vassileva
- first_name: Stephan
  full_name: Schmid, Stephan P
  last_name: Schmid
- first_name: Sara
  full_name: Maes, Sara
  last_name: Maes
- first_name: Boris
  full_name: Parizot, Boris
  last_name: Parizot
- first_name: Satoshi
  full_name: Naramoto, Satoshi
  last_name: Naramoto
- first_name: Zoltan
  full_name: Magyar, Zoltan
  last_name: Magyar
- first_name: Claire
  full_name: Lessa Alvim Kamei, Claire
  last_name: Lessa Alvim Kamei
- first_name: Csaba
  full_name: Koncz, Csaba
  last_name: Koncz
- first_name: Laszlo
  full_name: Bögre, Laszlo
  last_name: Bögre
- first_name: Geert
  full_name: Persiau, Geert
  last_name: Persiau
- first_name: Geert
  full_name: De Jaeger, Geert
  last_name: De Jaeger
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Rüdiger
  full_name: Simon, Rüdiger
  last_name: Simon
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Lieven
  full_name: de Veyldera, Lieven
  last_name: De Veyldera
citation:
  ama: Berckmans B, Vassileva V, Schmid S, et al. Auxin Dependent cell cycle reactivation
    through transcriptional regulation of arabidopsis E2Fa by lateral organ boundary
    proteins. <i>Plant Cell</i>. 2011;23(10):3671-3683. doi:<a href="https://doi.org/10.1105/tpc.111.088377">10.1105/tpc.111.088377</a>
  apa: Berckmans, B., Vassileva, V., Schmid, S., Maes, S., Parizot, B., Naramoto,
    S., … De Veyldera, L. (2011). Auxin Dependent cell cycle reactivation through
    transcriptional regulation of arabidopsis E2Fa by lateral organ boundary proteins.
    <i>Plant Cell</i>. American Society of Plant Biologists. <a href="https://doi.org/10.1105/tpc.111.088377">https://doi.org/10.1105/tpc.111.088377</a>
  chicago: Berckmans, Barbara, Valya Vassileva, Stephan Schmid, Sara Maes, Boris Parizot,
    Satoshi Naramoto, Zoltan Magyar, et al. “Auxin Dependent Cell Cycle Reactivation
    through Transcriptional Regulation of Arabidopsis E2Fa by Lateral Organ Boundary
    Proteins.” <i>Plant Cell</i>. American Society of Plant Biologists, 2011. <a href="https://doi.org/10.1105/tpc.111.088377">https://doi.org/10.1105/tpc.111.088377</a>.
  ieee: B. Berckmans <i>et al.</i>, “Auxin Dependent cell cycle reactivation through
    transcriptional regulation of arabidopsis E2Fa by lateral organ boundary proteins,”
    <i>Plant Cell</i>, vol. 23, no. 10. American Society of Plant Biologists, pp.
    3671–3683, 2011.
  ista: Berckmans B, Vassileva V, Schmid S, Maes S, Parizot B, Naramoto S, Magyar
    Z, Lessa Alvim Kamei C, Koncz C, Bögre L, Persiau G, De Jaeger G, Friml J, Simon
    R, Beeckman T, De Veyldera L. 2011. Auxin Dependent cell cycle reactivation through
    transcriptional regulation of arabidopsis E2Fa by lateral organ boundary proteins.
    Plant Cell. 23(10), 3671–3683.
  mla: Berckmans, Barbara, et al. “Auxin Dependent Cell Cycle Reactivation through
    Transcriptional Regulation of Arabidopsis E2Fa by Lateral Organ Boundary Proteins.”
    <i>Plant Cell</i>, vol. 23, no. 10, American Society of Plant Biologists, 2011,
    pp. 3671–83, doi:<a href="https://doi.org/10.1105/tpc.111.088377">10.1105/tpc.111.088377</a>.
  short: B. Berckmans, V. Vassileva, S. Schmid, S. Maes, B. Parizot, S. Naramoto,
    Z. Magyar, C. Lessa Alvim Kamei, C. Koncz, L. Bögre, G. Persiau, G. De Jaeger,
    J. Friml, R. Simon, T. Beeckman, L. De Veyldera, Plant Cell 23 (2011) 3671–3683.
date_created: 2018-12-11T12:01:24Z
date_published: 2011-10-14T00:00:00Z
date_updated: 2021-01-12T07:41:04Z
day: '14'
doi: 10.1105/tpc.111.088377
extern: 1
intvolume: '        23'
issue: '10'
month: '10'
page: 3671 - 3683
publication: Plant Cell
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '3598'
quality_controlled: 0
status: public
title: Auxin Dependent cell cycle reactivation through transcriptional regulation
  of arabidopsis E2Fa by lateral organ boundary proteins
type: journal_article
volume: 23
year: '2011'
...
---
_id: '3103'
abstract:
- lang: eng
  text: Endocytosis in plants has an essential role not only for basic cellular functions
    but also for growth and development, hormonal signaling and communication with
    the environment including nutrient delivery, toxin avoidance, and pathogen defense.
    The major endocytic mechanism in plants depends on the coat protein clathrin.
    It starts by clathrin-coated vesicle formation at the plasma membrane, where specific
    cargoes are recognized and packaged for internalization. Recently, genetic, biochemical
    and advanced microscopy studies provided initial insights into mechanisms and
    roles of clathrin-mediated endocytosis in plants. Here we summarize the present
    state of knowledge and compare mechanisms of clathrin-mediated endocytosis in
    plants with animal and yeast paradigms as well as review plant-specific regulations
    and roles of this process.
author:
- first_name: Xu
  full_name: Chen, Xu
  id: 4E5ADCAA-F248-11E8-B48F-1D18A9856A87
  last_name: Chen
- first_name: Niloufer
  full_name: Irani, Niloufer
  last_name: Irani
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: 'Chen X, Irani N, Friml J. Clathrin-mediated endocytosis: The gateway into
    plant cells. <i>Current Opinion in Plant Biology</i>. 2011;14(6):674-682. doi:<a
    href="https://doi.org/10.1016/j.pbi.2011.08.006">10.1016/j.pbi.2011.08.006</a>'
  apa: 'Chen, X., Irani, N., &#38; Friml, J. (2011). Clathrin-mediated endocytosis:
    The gateway into plant cells. <i>Current Opinion in Plant Biology</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.pbi.2011.08.006">https://doi.org/10.1016/j.pbi.2011.08.006</a>'
  chicago: 'Chen, Xu, Niloufer Irani, and Jiří Friml. “Clathrin-Mediated Endocytosis:
    The Gateway into Plant Cells.” <i>Current Opinion in Plant Biology</i>. Elsevier,
    2011. <a href="https://doi.org/10.1016/j.pbi.2011.08.006">https://doi.org/10.1016/j.pbi.2011.08.006</a>.'
  ieee: 'X. Chen, N. Irani, and J. Friml, “Clathrin-mediated endocytosis: The gateway
    into plant cells,” <i>Current Opinion in Plant Biology</i>, vol. 14, no. 6. Elsevier,
    pp. 674–682, 2011.'
  ista: 'Chen X, Irani N, Friml J. 2011. Clathrin-mediated endocytosis: The gateway
    into plant cells. Current Opinion in Plant Biology. 14(6), 674–682.'
  mla: 'Chen, Xu, et al. “Clathrin-Mediated Endocytosis: The Gateway into Plant Cells.”
    <i>Current Opinion in Plant Biology</i>, vol. 14, no. 6, Elsevier, 2011, pp. 674–82,
    doi:<a href="https://doi.org/10.1016/j.pbi.2011.08.006">10.1016/j.pbi.2011.08.006</a>.'
  short: X. Chen, N. Irani, J. Friml, Current Opinion in Plant Biology 14 (2011) 674–682.
date_created: 2018-12-11T12:01:24Z
date_published: 2011-12-01T00:00:00Z
date_updated: 2021-01-12T07:41:05Z
day: '01'
doi: 10.1016/j.pbi.2011.08.006
extern: '1'
intvolume: '        14'
issue: '6'
language:
- iso: eng
month: '12'
oa_version: None
page: 674 - 682
publication: Current Opinion in Plant Biology
publication_status: published
publisher: Elsevier
publist_id: '3596'
quality_controlled: '1'
status: public
title: 'Clathrin-mediated endocytosis: The gateway into plant cells'
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 14
year: '2011'
...
---
_id: '3138'
abstract:
- lang: eng
  text: Hippocampal sharp waves (SPWs) and associated fast (&quot;ripple&quot;) oscillations
    (SPW-Rs) in the CA1 region are among the most synchronous physiological patterns
    in the mammalian brain. Using two-dimensional arrays of electrodes for recording
    local field potentials and unit discharges in freely moving rats, we studied the
    emergence of ripple oscillations (140-220 Hz) and compared their origin and cellular-synaptic
    mechanisms with fast gamma oscillations (90-140 Hz). We show that (1) hippocampal
    SPW-Rs and fast gamma oscillations are quantitatively distinct patterns but involve
    the same networks and share similar mechanisms; (2) both the frequency and magnitude
    of fast oscillations are positively correlated with the magnitude of SPWs; (3)
    during both ripples and fast gamma oscillations the frequency of network oscillation
    is higher in CA1 than in CA3; and (4) the emergence of CA3 population bursts,
    a prerequisite for SPW-Rs, is biased by activity patterns in the dentate gyrus
    and entorhinal cortex, with the highest probability of ripples associated with
    an &quot;optimum&quot; level of dentate gamma power. We hypothesize that each
    hippocampal subnetwork possesses distinct resonant properties, tuned by the magnitude
    of the excitatory drive.
author:
- first_name: David
  full_name: Sullivan, David W
  last_name: Sullivan
- first_name: Jozsef L
  full_name: Jozsef Csicsvari
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
- first_name: Kenji
  full_name: Mizuseki, Kenji
  last_name: Mizuseki
- first_name: Sean
  full_name: Montgomery, Sean M
  last_name: Montgomery
- first_name: Kamran
  full_name: Diba, Kamran
  last_name: Diba
- first_name: György
  full_name: Buzsáki, György
  last_name: Buzsáki
citation:
  ama: Sullivan D, Csicsvari JL, Mizuseki K, Montgomery S, Diba K, Buzsáki G. Relationships
    between hippocampal sharp waves ripples and fast gamma oscillation Influence of
    dentate and entorhinal cortical activity. <i>Journal of Neuroscience</i>. 2011;31(23):8605-8616.
    doi:<a href="https://doi.org/10.1523/JNEUROSCI.0294-11.2011">10.1523/JNEUROSCI.0294-11.2011</a>
  apa: Sullivan, D., Csicsvari, J. L., Mizuseki, K., Montgomery, S., Diba, K., &#38;
    Buzsáki, G. (2011). Relationships between hippocampal sharp waves ripples and
    fast gamma oscillation Influence of dentate and entorhinal cortical activity.
    <i>Journal of Neuroscience</i>. Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.0294-11.2011">https://doi.org/10.1523/JNEUROSCI.0294-11.2011</a>
  chicago: Sullivan, David, Jozsef L Csicsvari, Kenji Mizuseki, Sean Montgomery, Kamran
    Diba, and György Buzsáki. “Relationships between Hippocampal Sharp Waves Ripples
    and Fast Gamma Oscillation Influence of Dentate and Entorhinal Cortical Activity.”
    <i>Journal of Neuroscience</i>. Society for Neuroscience, 2011. <a href="https://doi.org/10.1523/JNEUROSCI.0294-11.2011">https://doi.org/10.1523/JNEUROSCI.0294-11.2011</a>.
  ieee: D. Sullivan, J. L. Csicsvari, K. Mizuseki, S. Montgomery, K. Diba, and G.
    Buzsáki, “Relationships between hippocampal sharp waves ripples and fast gamma
    oscillation Influence of dentate and entorhinal cortical activity,” <i>Journal
    of Neuroscience</i>, vol. 31, no. 23. Society for Neuroscience, pp. 8605–8616,
    2011.
  ista: Sullivan D, Csicsvari JL, Mizuseki K, Montgomery S, Diba K, Buzsáki G. 2011.
    Relationships between hippocampal sharp waves ripples and fast gamma oscillation
    Influence of dentate and entorhinal cortical activity. Journal of Neuroscience.
    31(23), 8605–8616.
  mla: Sullivan, David, et al. “Relationships between Hippocampal Sharp Waves Ripples
    and Fast Gamma Oscillation Influence of Dentate and Entorhinal Cortical Activity.”
    <i>Journal of Neuroscience</i>, vol. 31, no. 23, Society for Neuroscience, 2011,
    pp. 8605–16, doi:<a href="https://doi.org/10.1523/JNEUROSCI.0294-11.2011">10.1523/JNEUROSCI.0294-11.2011</a>.
  short: D. Sullivan, J.L. Csicsvari, K. Mizuseki, S. Montgomery, K. Diba, G. Buzsáki,
    Journal of Neuroscience 31 (2011) 8605–8616.
date_created: 2018-12-11T12:01:36Z
date_published: 2011-06-08T00:00:00Z
date_updated: 2021-01-12T07:41:19Z
day: '08'
doi: 10.1523/JNEUROSCI.0294-11.2011
extern: 1
intvolume: '        31'
issue: '23'
month: '06'
page: 8605 - 8616
publication: Journal of Neuroscience
publication_status: published
publisher: Society for Neuroscience
publist_id: '3559'
quality_controlled: 0
status: public
title: Relationships between hippocampal sharp waves ripples and fast gamma oscillation
  Influence of dentate and entorhinal cortical activity
type: journal_article
volume: 31
year: '2011'
...
---
_id: '3145'
abstract:
- lang: eng
  text: Microinjection of recombinant DNA into zygotic pronuclei has been widely used
    for producing transgenic mice. However, with this method, the insertion site,
    integrity, and copy number of the transgene cannot be controlled. Here, we present
    an integrase-based approach to produce transgenic mice via pronuclear injection,
    whereby an intact single-copy transgene can be inserted into predetermined chromosomal
    loci with high efficiency (up to 40%), and faithfully transmitted through generations.
    We show that neighboring transgenic elements and bacterial DNA within the transgene
    cause profound silencing and expression variability of the transgenic marker.
    Removal of these undesirable elements leads to global high-level marker expression
    from transgenes driven by a ubiquitous promoter. We also obtained faithful marker
    expression from a tissue-specific promoter. The technique presented here will
    greatly facilitate murine transgenesis and precise structure/function dissection
    of mammalian gene function and regulation in vivo.
author:
- first_name: Bosiljka
  full_name: Tasic, Bosiljka
  last_name: Tasic
- first_name: Simon
  full_name: Simon Hippenmeyer
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
- first_name: Charlene
  full_name: Wang, Charlene
  last_name: Wang
- first_name: Matthew
  full_name: Gamboa, Matthew
  last_name: Gamboa
- first_name: Hui
  full_name: Zong, Hui
  last_name: Zong
- first_name: Yanru
  full_name: Chen-Tsai, Yanru
  last_name: Chen Tsai
- first_name: Liqun
  full_name: Luo, Liqun
  last_name: Luo
citation:
  ama: Tasic B, Hippenmeyer S, Wang C, et al. Site specific integrase mediated transgenesis
    in mice via pronuclear injection. <i>PNAS</i>. 2011;108(19):7902-7907. doi:<a
    href="https://doi.org/10.1073/pnas.1019507108">10.1073/pnas.1019507108</a>
  apa: Tasic, B., Hippenmeyer, S., Wang, C., Gamboa, M., Zong, H., Chen Tsai, Y.,
    &#38; Luo, L. (2011). Site specific integrase mediated transgenesis in mice via
    pronuclear injection. <i>PNAS</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1019507108">https://doi.org/10.1073/pnas.1019507108</a>
  chicago: Tasic, Bosiljka, Simon Hippenmeyer, Charlene Wang, Matthew Gamboa, Hui
    Zong, Yanru Chen Tsai, and Liqun Luo. “Site Specific Integrase Mediated Transgenesis
    in Mice via Pronuclear Injection.” <i>PNAS</i>. National Academy of Sciences,
    2011. <a href="https://doi.org/10.1073/pnas.1019507108">https://doi.org/10.1073/pnas.1019507108</a>.
  ieee: B. Tasic <i>et al.</i>, “Site specific integrase mediated transgenesis in
    mice via pronuclear injection,” <i>PNAS</i>, vol. 108, no. 19. National Academy
    of Sciences, pp. 7902–7907, 2011.
  ista: Tasic B, Hippenmeyer S, Wang C, Gamboa M, Zong H, Chen Tsai Y, Luo L. 2011.
    Site specific integrase mediated transgenesis in mice via pronuclear injection.
    PNAS. 108(19), 7902–7907.
  mla: Tasic, Bosiljka, et al. “Site Specific Integrase Mediated Transgenesis in Mice
    via Pronuclear Injection.” <i>PNAS</i>, vol. 108, no. 19, National Academy of
    Sciences, 2011, pp. 7902–07, doi:<a href="https://doi.org/10.1073/pnas.1019507108">10.1073/pnas.1019507108</a>.
  short: B. Tasic, S. Hippenmeyer, C. Wang, M. Gamboa, H. Zong, Y. Chen Tsai, L. Luo,
    PNAS 108 (2011) 7902–7907.
date_created: 2018-12-11T12:01:39Z
date_published: 2011-05-10T00:00:00Z
date_updated: 2021-01-12T07:41:22Z
day: '10'
doi: 10.1073/pnas.1019507108
extern: 1
intvolume: '       108'
issue: '19'
month: '05'
page: 7902 - 7907
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3549'
quality_controlled: 0
status: public
title: Site specific integrase mediated transgenesis in mice via pronuclear injection
type: journal_article
volume: 108
year: '2011'
...
---
_id: '3147'
abstract:
- lang: eng
  text: Cancer cell of origin is difficult to identify by analyzing cells within terminal
    stage tumors, whose identity could be concealed by the acquired plasticity. Thus,
    an ideal approach to identify the cell of origin is to analyze proliferative abnormalities
    in distinct lineages prior to malignancy. Here, we use mosaic analysis with double
    markers (MADM) in mice to model gliomagenesis by initiating concurrent p53/Nf1
    mutations sporadically in neural stem cells (NSCs). Surprisingly, MADM-based lineage
    tracing revealed significant aberrant growth prior to malignancy only in oligodendrocyte
    precursor cells (OPCs), but not in any other NSC-derived lineages or NSCs themselves.
    Upon tumor formation, phenotypic and transcriptome analyses of tumor cells revealed
    salient OPC features. Finally, introducing the same p53/Nf1 mutations directly
    into OPCs consistently led to gliomagenesis. Our findings suggest OPCs as the
    cell of origin in this model, even when initial mutations occur in NSCs, and highlight
    the importance of analyzing premalignant stages to identify the cancer cell of
    origin.
author:
- first_name: Chong
  full_name: Liu, Chong
  last_name: Liu
- first_name: Jonathan
  full_name: Sage, Jonathan C
  last_name: Sage
- first_name: Michael
  full_name: Miller, Michael R
  last_name: Miller
- first_name: Roel
  full_name: Verhaak, Roel G
  last_name: Verhaak
- first_name: Simon
  full_name: Simon Hippenmeyer
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
- first_name: Hannes
  full_name: Vogel, Hannes
  last_name: Vogel
- first_name: Oded
  full_name: Foreman, Oded
  last_name: Foreman
- first_name: Roderick
  full_name: Bronson, Roderick T
  last_name: Bronson
- first_name: Akiko
  full_name: Nishiyama, Akiko
  last_name: Nishiyama
- first_name: Liqun
  full_name: Luo, Liqun
  last_name: Luo
- first_name: Hui
  full_name: Zong, Hui
  last_name: Zong
citation:
  ama: Liu C, Sage J, Miller M, et al. Mosaic analysis with double markers reveals
    tumor cell of origin in glioma. <i>Cell</i>. 2011;146(2):209-221. doi:<a href="https://doi.org/10.1016/j.cell.2011.06.014">10.1016/j.cell.2011.06.014</a>
  apa: Liu, C., Sage, J., Miller, M., Verhaak, R., Hippenmeyer, S., Vogel, H., … Zong,
    H. (2011). Mosaic analysis with double markers reveals tumor cell of origin in
    glioma. <i>Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.cell.2011.06.014">https://doi.org/10.1016/j.cell.2011.06.014</a>
  chicago: Liu, Chong, Jonathan Sage, Michael Miller, Roel Verhaak, Simon Hippenmeyer,
    Hannes Vogel, Oded Foreman, et al. “Mosaic Analysis with Double Markers Reveals
    Tumor Cell of Origin in Glioma.” <i>Cell</i>. Cell Press, 2011. <a href="https://doi.org/10.1016/j.cell.2011.06.014">https://doi.org/10.1016/j.cell.2011.06.014</a>.
  ieee: C. Liu <i>et al.</i>, “Mosaic analysis with double markers reveals tumor cell
    of origin in glioma,” <i>Cell</i>, vol. 146, no. 2. Cell Press, pp. 209–221, 2011.
  ista: Liu C, Sage J, Miller M, Verhaak R, Hippenmeyer S, Vogel H, Foreman O, Bronson
    R, Nishiyama A, Luo L, Zong H. 2011. Mosaic analysis with double markers reveals
    tumor cell of origin in glioma. Cell. 146(2), 209–221.
  mla: Liu, Chong, et al. “Mosaic Analysis with Double Markers Reveals Tumor Cell
    of Origin in Glioma.” <i>Cell</i>, vol. 146, no. 2, Cell Press, 2011, pp. 209–21,
    doi:<a href="https://doi.org/10.1016/j.cell.2011.06.014">10.1016/j.cell.2011.06.014</a>.
  short: C. Liu, J. Sage, M. Miller, R. Verhaak, S. Hippenmeyer, H. Vogel, O. Foreman,
    R. Bronson, A. Nishiyama, L. Luo, H. Zong, Cell 146 (2011) 209–221.
date_created: 2018-12-11T12:01:40Z
date_published: 2011-07-22T00:00:00Z
date_updated: 2021-01-12T07:41:23Z
day: '22'
doi: 10.1016/j.cell.2011.06.014
extern: 1
intvolume: '       146'
issue: '2'
month: '07'
page: 209 - 221
publication: Cell
publication_status: published
publisher: Cell Press
publist_id: '3548'
quality_controlled: 0
status: public
title: Mosaic analysis with double markers reveals tumor cell of origin in glioma
type: journal_article
volume: 146
year: '2011'
...
---
_id: '3154'
abstract:
- lang: eng
  text: Regulated adhesion between cells and their environment is critical for normal
    cell migration. We have identified mutations in a gene encoding the Drosophila
    hydrogen peroxide (H2O2)-degrading enzyme Jafrac1, which lead to germ cell adhesion
    defects. During gastrulation, primordial germ cells (PGCs) associate tightly with
    the invaginating midgut primordium as it enters the embryo; however, in embryos
    from jafrac1 mutant mothers this association is disrupted, leaving some PGCs trailing
    on the outside of the embryo. We observed similar phenotypes in embryos from DE-cadherin/shotgun
    (shg) mutant mothers and were able to rescue the jafrac1 phenotype by increasing
    DE-cadherin levels. This and our biochemical evidence strongly suggest that Jafrac1-mediated
    reduction of H2O2 is required to maintain DE-cadherin protein levels in the early
    embryo. Our results present in vivo evidence of a peroxiredoxin regulating DE-cadherin-mediated
    adhesion.
author:
- first_name: Matthew
  full_name: DeGennaro, Matthew
  last_name: Degennaro
- first_name: Thomas
  full_name: Hurd, Thomas R
  last_name: Hurd
- first_name: Daria E
  full_name: Daria Siekhaus
  id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
  last_name: Siekhaus
  orcid: 0000-0001-8323-8353
- first_name: Benoit
  full_name: Biteau, Benoit
  last_name: Biteau
- first_name: Heinrich
  full_name: Jasper, Heinrich
  last_name: Jasper
- first_name: Ruth
  full_name: Lehmann, Ruth
  last_name: Lehmann
citation:
  ama: Degennaro M, Hurd T, Siekhaus DE, Biteau B, Jasper H, Lehmann R. Peroxiredoxin
    stabilization of DE-cadherin promotes primordial germ cell adhesion. <i>Developmental
    Cell</i>. 2011;20(2):233-243. doi:<a href="https://doi.org/10.1016/j.devcel.2010.12.007">10.1016/j.devcel.2010.12.007</a>
  apa: Degennaro, M., Hurd, T., Siekhaus, D. E., Biteau, B., Jasper, H., &#38; Lehmann,
    R. (2011). Peroxiredoxin stabilization of DE-cadherin promotes primordial germ
    cell adhesion. <i>Developmental Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.devcel.2010.12.007">https://doi.org/10.1016/j.devcel.2010.12.007</a>
  chicago: Degennaro, Matthew, Thomas Hurd, Daria E Siekhaus, Benoit Biteau, Heinrich
    Jasper, and Ruth Lehmann. “Peroxiredoxin Stabilization of DE-Cadherin Promotes
    Primordial Germ Cell Adhesion.” <i>Developmental Cell</i>. Cell Press, 2011. <a
    href="https://doi.org/10.1016/j.devcel.2010.12.007">https://doi.org/10.1016/j.devcel.2010.12.007</a>.
  ieee: M. Degennaro, T. Hurd, D. E. Siekhaus, B. Biteau, H. Jasper, and R. Lehmann,
    “Peroxiredoxin stabilization of DE-cadherin promotes primordial germ cell adhesion,”
    <i>Developmental Cell</i>, vol. 20, no. 2. Cell Press, pp. 233–243, 2011.
  ista: Degennaro M, Hurd T, Siekhaus DE, Biteau B, Jasper H, Lehmann R. 2011. Peroxiredoxin
    stabilization of DE-cadherin promotes primordial germ cell adhesion. Developmental
    Cell. 20(2), 233–243.
  mla: Degennaro, Matthew, et al. “Peroxiredoxin Stabilization of DE-Cadherin Promotes
    Primordial Germ Cell Adhesion.” <i>Developmental Cell</i>, vol. 20, no. 2, Cell
    Press, 2011, pp. 233–43, doi:<a href="https://doi.org/10.1016/j.devcel.2010.12.007">10.1016/j.devcel.2010.12.007</a>.
  short: M. Degennaro, T. Hurd, D.E. Siekhaus, B. Biteau, H. Jasper, R. Lehmann, Developmental
    Cell 20 (2011) 233–243.
date_created: 2018-12-11T12:01:42Z
date_published: 2011-02-15T00:00:00Z
date_updated: 2021-01-12T07:41:26Z
day: '15'
doi: 10.1016/j.devcel.2010.12.007
extern: 1
intvolume: '        20'
issue: '2'
month: '02'
page: 233 - 243
publication: Developmental Cell
publication_status: published
publisher: Cell Press
publist_id: '3541'
quality_controlled: 0
status: public
title: Peroxiredoxin stabilization of DE-cadherin promotes primordial germ cell adhesion
type: journal_article
volume: 20
year: '2011'
...
---
_id: '3163'
abstract:
- lang: eng
  text: We study multi-label prediction for structured output sets, a problem that
    occurs, for example, in object detection in images, secondary structure prediction
    in computational biology, and graph matching with symmetries. Conventional multilabel
    classification techniques are typically not applicable in this situation, because
    they require explicit enumeration of the label set, which is infeasible in case
    of structured outputs. Relying on techniques originally designed for single-label
    structured prediction, in particular structured support vector machines, results
    in reduced prediction accuracy, or leads to infeasible optimization problems.
    In this work we derive a maximum-margin training formulation for multi-label structured
    prediction that remains computationally tractable while achieving high prediction
    accuracy. It also shares most beneficial properties with single-label maximum-margin
    approaches, in particular formulation as a convex optimization problem, efficient
    working set training, and PAC-Bayesian generalization bounds.
author:
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
citation:
  ama: 'Lampert C. Maximum margin multi-label structured prediction. In: Neural Information
    Processing Systems; 2011.'
  apa: 'Lampert, C. (2011). Maximum margin multi-label structured prediction. Presented
    at the NIPS: Neural Information Processing Systems, Granada, Spain: Neural Information
    Processing Systems.'
  chicago: Lampert, Christoph. “Maximum Margin Multi-Label Structured Prediction.”
    Neural Information Processing Systems, 2011.
  ieee: 'C. Lampert, “Maximum margin multi-label structured prediction,” presented
    at the NIPS: Neural Information Processing Systems, Granada, Spain, 2011.'
  ista: 'Lampert C. 2011. Maximum margin multi-label structured prediction. NIPS:
    Neural Information Processing Systems.'
  mla: Lampert, Christoph. <i>Maximum Margin Multi-Label Structured Prediction</i>.
    Neural Information Processing Systems, 2011.
  short: C. Lampert, in:, Neural Information Processing Systems, 2011.
conference:
  end_date: 2011-12-14
  location: Granada, Spain
  name: 'NIPS: Neural Information Processing Systems'
  start_date: 2011-12-12
date_created: 2018-12-11T12:01:45Z
date_published: 2011-12-01T00:00:00Z
date_updated: 2023-10-17T11:47:35Z
day: '01'
department:
- _id: ChLa
language:
- iso: eng
month: '12'
oa_version: None
publication_status: published
publisher: Neural Information Processing Systems
publist_id: '3522'
quality_controlled: '1'
related_material:
  record:
  - id: '3322'
    relation: later_version
    status: public
scopus_import: 1
status: public
title: Maximum margin multi-label structured prediction
type: conference
user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87
year: '2011'
...
---
_id: '3204'
abstract:
- lang: eng
  text: 'We introduce a new class of functions that can be minimized in polynomial
    time in the value oracle model. These are functions f satisfying f(x) + f(y) ≥
    f(x ∏ y) + f(x ∐ y) where the domain of each variable x i corresponds to nodes
    of a rooted binary tree, and operations ∏,∐ are defined with respect to this tree.
    Special cases include previously studied L-convex and bisubmodular functions,
    which can be obtained with particular choices of trees. We present a polynomial-time
    algorithm for minimizing functions in the new class. It combines Murota''s steepest
    descent algorithm for L-convex functions with bisubmodular minimization algorithms. '
alternative_title:
- LNCS
author:
- first_name: Vladimir
  full_name: Vladimir Kolmogorov
  id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kolmogorov
citation:
  ama: 'Kolmogorov V. Submodularity on a tree: Unifying Submodularity on a tree: Unifying
    L-convex and bisubmodular functions convex and bisubmodular functions. In: Vol
    6907. Springer; 2011:400-411. doi:<a href="https://doi.org/10.1007/978-3-642-22993-0_37">10.1007/978-3-642-22993-0_37</a>'
  apa: 'Kolmogorov, V. (2011). Submodularity on a tree: Unifying Submodularity on
    a tree: Unifying L-convex and bisubmodular functions convex and bisubmodular functions
    (Vol. 6907, pp. 400–411). Presented at the MFCS: Mathematical Foundations of Computer
    Science, Springer. <a href="https://doi.org/10.1007/978-3-642-22993-0_37">https://doi.org/10.1007/978-3-642-22993-0_37</a>'
  chicago: 'Kolmogorov, Vladimir. “Submodularity on a Tree: Unifying Submodularity
    on a Tree: Unifying L-Convex and Bisubmodular Functions Convex and Bisubmodular
    Functions,” 6907:400–411. Springer, 2011. <a href="https://doi.org/10.1007/978-3-642-22993-0_37">https://doi.org/10.1007/978-3-642-22993-0_37</a>.'
  ieee: 'V. Kolmogorov, “Submodularity on a tree: Unifying Submodularity on a tree:
    Unifying L-convex and bisubmodular functions convex and bisubmodular functions,”
    presented at the MFCS: Mathematical Foundations of Computer Science, 2011, vol.
    6907, pp. 400–411.'
  ista: 'Kolmogorov V. 2011. Submodularity on a tree: Unifying Submodularity on a
    tree: Unifying L-convex and bisubmodular functions convex and bisubmodular functions.
    MFCS: Mathematical Foundations of Computer Science, LNCS, vol. 6907, 400–411.'
  mla: 'Kolmogorov, Vladimir. <i>Submodularity on a Tree: Unifying Submodularity on
    a Tree: Unifying L-Convex and Bisubmodular Functions Convex and Bisubmodular Functions</i>.
    Vol. 6907, Springer, 2011, pp. 400–11, doi:<a href="https://doi.org/10.1007/978-3-642-22993-0_37">10.1007/978-3-642-22993-0_37</a>.'
  short: V. Kolmogorov, in:, Springer, 2011, pp. 400–411.
conference:
  name: 'MFCS: Mathematical Foundations of Computer Science'
date_created: 2018-12-11T12:02:00Z
date_published: 2011-08-09T00:00:00Z
date_updated: 2021-01-12T07:41:47Z
day: '09'
doi: 10.1007/978-3-642-22993-0_37
extern: 1
intvolume: '      6907'
main_file_link:
- open_access: '0'
  url: http://arxiv.org/pdf/1007.1229v3
month: '08'
page: 400 - 411
publication_status: published
publisher: Springer
publist_id: '3478'
quality_controlled: 0
status: public
title: 'Submodularity on a tree: Unifying Submodularity on a tree: Unifying L-convex
  and bisubmodular functions convex and bisubmodular functions'
type: conference
volume: 6907
year: '2011'
...
---
_id: '3205'
abstract:
- lang: eng
  text: This paper proposes a novel Linear Programming (LP) based algorithm, called
    Dynamic Tree-Block Coordinate Ascent (DT-BCA), for performing maximum a posteriori
    (MAP) inference in probabilistic graphical models. Unlike traditional message
    passing algorithms, which operate uniformly on the whole factor graph, our method
    dynamically chooses regions of the factor graph on which to focus message-passing
    efforts. We propose two criteria for selecting regions, including an efficiently
    computable upper-bound on the increase in the objective possible by passing messages
    in any particular region. This bound is derived from the theory of primal-dual
    methods from combinatorial optimization, and the forest that maximizes the bounds
    can be chosen efficiently using a maximum-spanning-tree-like algorithm. Experimental
    results show that our dynamic schedules significantly speed up state-of-the-art
    LP-based message-passing algorithms on a wide variety of real-world problems.
author:
- first_name: Daniel
  full_name: Tarlow, Daniel
  last_name: Tarlow
- first_name: Druv
  full_name: Batra, Druv
  last_name: Batra
- first_name: Pushmeet
  full_name: Kohli, Pushmeet
  last_name: Kohli
- first_name: Vladimir
  full_name: Vladimir Kolmogorov
  id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kolmogorov
citation:
  ama: 'Tarlow D, Batra D, Kohli P, Kolmogorov V. Dynamic tree block coordinate ascent.
    In: Omnipress; 2011:113-120.'
  apa: 'Tarlow, D., Batra, D., Kohli, P., &#38; Kolmogorov, V. (2011). Dynamic tree
    block coordinate ascent (pp. 113–120). Presented at the ICML: International Conference
    on Machine Learning, Omnipress.'
  chicago: Tarlow, Daniel, Druv Batra, Pushmeet Kohli, and Vladimir Kolmogorov. “Dynamic
    Tree Block Coordinate Ascent,” 113–20. Omnipress, 2011.
  ieee: 'D. Tarlow, D. Batra, P. Kohli, and V. Kolmogorov, “Dynamic tree block coordinate
    ascent,” presented at the ICML: International Conference on Machine Learning,
    2011, pp. 113–120.'
  ista: 'Tarlow D, Batra D, Kohli P, Kolmogorov V. 2011. Dynamic tree block coordinate
    ascent. ICML: International Conference on Machine Learning, 113–120.'
  mla: Tarlow, Daniel, et al. <i>Dynamic Tree Block Coordinate Ascent</i>. Omnipress,
    2011, pp. 113–20.
  short: D. Tarlow, D. Batra, P. Kohli, V. Kolmogorov, in:, Omnipress, 2011, pp. 113–120.
conference:
  name: 'ICML: International Conference on Machine Learning'
date_created: 2018-12-11T12:02:00Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2021-01-12T07:41:47Z
day: '01'
extern: 1
main_file_link:
- open_access: '0'
  url: http://ttic.uchicago.edu/~dbatra/publications/assets/tbkk_icml11.pdf
month: '01'
page: 113 - 120
publication_status: published
publisher: Omnipress
publist_id: '3475'
quality_controlled: 0
status: public
title: Dynamic tree block coordinate ascent
type: conference
year: '2011'
...
---
_id: '3206'
abstract:
- lang: eng
  text: In this paper we address the problem of finding the most probable state of
    discrete Markov random field (MRF) with associative pairwise terms. Although of
    practical importance, this problem is known to be NP-hard in general. We propose
    a new type of MRF decomposition, submod-ular decomposition (SMD). Unlike existing
    decomposition approaches SMD decomposes the initial problem into sub-problems
    corresponding to a specific class label while preserving the graph structure of
    each subproblem. Such decomposition enables us to take into account several types
    of global constraints in an efficient manner. We study theoretical properties
    of the proposed approach and demonstrate its applicability on a number of problems.
author:
- first_name: Anton
  full_name: Osokin, Anton
  last_name: Osokin
- first_name: Dmitry
  full_name: Vetrov, Dmitry
  last_name: Vetrov
- first_name: Vladimir
  full_name: Vladimir Kolmogorov
  id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kolmogorov
citation:
  ama: 'Osokin A, Vetrov D, Kolmogorov V. Submodular decomposition framework for inference
    in associative Markov networks with global constraints. In: IEEE; 2011:1889-1896.
    doi:<a href="https://doi.org/10.1109/CVPR.2011.5995361">10.1109/CVPR.2011.5995361</a>'
  apa: 'Osokin, A., Vetrov, D., &#38; Kolmogorov, V. (2011). Submodular decomposition
    framework for inference in associative Markov networks with global constraints
    (pp. 1889–1896). Presented at the CVPR: Computer Vision and Pattern Recognition,
    IEEE. <a href="https://doi.org/10.1109/CVPR.2011.5995361">https://doi.org/10.1109/CVPR.2011.5995361</a>'
  chicago: Osokin, Anton, Dmitry Vetrov, and Vladimir Kolmogorov. “Submodular Decomposition
    Framework for Inference in Associative Markov Networks with Global Constraints,”
    1889–96. IEEE, 2011. <a href="https://doi.org/10.1109/CVPR.2011.5995361">https://doi.org/10.1109/CVPR.2011.5995361</a>.
  ieee: 'A. Osokin, D. Vetrov, and V. Kolmogorov, “Submodular decomposition framework
    for inference in associative Markov networks with global constraints,” presented
    at the CVPR: Computer Vision and Pattern Recognition, 2011, pp. 1889–1896.'
  ista: 'Osokin A, Vetrov D, Kolmogorov V. 2011. Submodular decomposition framework
    for inference in associative Markov networks with global constraints. CVPR: Computer
    Vision and Pattern Recognition, 1889–1896.'
  mla: Osokin, Anton, et al. <i>Submodular Decomposition Framework for Inference in
    Associative Markov Networks with Global Constraints</i>. IEEE, 2011, pp. 1889–96,
    doi:<a href="https://doi.org/10.1109/CVPR.2011.5995361">10.1109/CVPR.2011.5995361</a>.
  short: A. Osokin, D. Vetrov, V. Kolmogorov, in:, IEEE, 2011, pp. 1889–1896.
conference:
  name: 'CVPR: Computer Vision and Pattern Recognition'
date_created: 2018-12-11T12:02:00Z
date_published: 2011-08-22T00:00:00Z
date_updated: 2021-01-12T07:41:47Z
day: '22'
doi: 10.1109/CVPR.2011.5995361
extern: 1
main_file_link:
- open_access: '0'
  url: http://arxiv.org/pdf/1103.1077v1
month: '08'
page: 1889 - 1896
publication_status: published
publisher: IEEE
publist_id: '3476'
quality_controlled: 0
status: public
title: Submodular decomposition framework for inference in associative Markov networks
  with global constraints
type: conference
year: '2011'
...
---
_id: '3207'
abstract:
- lang: eng
  text: 'Cosegmentation is typically defined as the task of jointly segmenting something
    similar in a given set of images. Existing methods are too generic and so far
    have not demonstrated competitive results for any specific task. In this paper
    we overcome this limitation by adding two new aspects to cosegmentation: (1) the
    &quot;something&quot; has to be an object, and (2) the &quot;similarity&quot;
    measure is learned. In this way, we are able to achieve excellent results on the
    recently introduced iCoseg dataset, which contains small sets of images of either
    the same object instance or similar objects of the same class. The challenge of
    this dataset lies in the extreme changes in viewpoint, lighting, and object deformations
    within each set. We are able to considerably outperform several competitors. To
    achieve this performance, we borrow recent ideas from object recognition: the
    use of powerful features extracted from a pool of candidate object-like segmentations.
    We believe that our work will be beneficial to several application areas, such
    as image retrieval.'
author:
- first_name: Sara
  full_name: Vicente, Sara
  last_name: Vicente
- first_name: Carsten
  full_name: Rother, Carsten
  last_name: Rother
- first_name: Vladimir
  full_name: Vladimir Kolmogorov
  id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kolmogorov
citation:
  ama: 'Vicente S, Rother C, Kolmogorov V. Object cosegmentation. In: IEEE; 2011:2217-2224.
    doi:<a href="https://doi.org/10.1109/CVPR.2011.5995530">10.1109/CVPR.2011.5995530</a>'
  apa: 'Vicente, S., Rother, C., &#38; Kolmogorov, V. (2011). Object cosegmentation
    (pp. 2217–2224). Presented at the CVPR: Computer Vision and Pattern Recognition,
    IEEE. <a href="https://doi.org/10.1109/CVPR.2011.5995530">https://doi.org/10.1109/CVPR.2011.5995530</a>'
  chicago: Vicente, Sara, Carsten Rother, and Vladimir Kolmogorov. “Object Cosegmentation,”
    2217–24. IEEE, 2011. <a href="https://doi.org/10.1109/CVPR.2011.5995530">https://doi.org/10.1109/CVPR.2011.5995530</a>.
  ieee: 'S. Vicente, C. Rother, and V. Kolmogorov, “Object cosegmentation,” presented
    at the CVPR: Computer Vision and Pattern Recognition, 2011, pp. 2217–2224.'
  ista: 'Vicente S, Rother C, Kolmogorov V. 2011. Object cosegmentation. CVPR: Computer
    Vision and Pattern Recognition, 2217–2224.'
  mla: Vicente, Sara, et al. <i>Object Cosegmentation</i>. IEEE, 2011, pp. 2217–24,
    doi:<a href="https://doi.org/10.1109/CVPR.2011.5995530">10.1109/CVPR.2011.5995530</a>.
  short: S. Vicente, C. Rother, V. Kolmogorov, in:, IEEE, 2011, pp. 2217–2224.
conference:
  name: 'CVPR: Computer Vision and Pattern Recognition'
date_created: 2018-12-11T12:02:01Z
date_published: 2011-08-22T00:00:00Z
date_updated: 2021-01-12T07:41:48Z
day: '22'
doi: 10.1109/CVPR.2011.5995530
extern: 1
month: '08'
page: 2217 - 2224
publication_status: published
publisher: IEEE
publist_id: '3477'
quality_controlled: 0
status: public
title: Object cosegmentation
type: conference
year: '2011'
...
---
_id: '3236'
abstract:
- lang: eng
  text: 'If a cryptographic primitive remains secure even if ℓ bits about the secret
    key are leaked to the adversary, one would expect that at least one of n independent
    instantiations of the scheme remains secure given n·ℓ bits of leakage. This intuition
    has been proven true for schemes satisfying some special information-theoretic
    properties by Alwen et al. [Eurocrypt''10]. On the negative side, Lewko and Waters
    [FOCS''10] construct a CPA secure public-key encryption scheme for which this
    intuition fails. The counterexample of Lewko and Waters leaves open the interesting
    possibility that for any scheme there exists a constant c&gt;0, such that n fold
    repetition remains secure against c·n·ℓ bits of leakage. Furthermore, their counterexample
    requires the n copies of the encryption scheme to share a common reference parameter,
    leaving open the possibility that the intuition is true for all schemes without
    common setup. In this work we give a stronger counterexample ruling out these
    possibilities. We construct a signature scheme such that: 1. a single instantiation
    remains secure given ℓ = log(k) bits of leakage where k is a security parameter.
    2. any polynomial number of independent instantiations can be broken (in the strongest
    sense of key-recovery) given ℓ′ = poly(k) bits of leakage. Note that ℓ does not
    depend on the number of instances. The computational assumption underlying our
    counterexample is that non-interactive computationally sound proofs exist. Moreover,
    under a stronger (non-standard) assumption about such proofs, our counterexample
    does not require a common reference parameter. The underlying idea of our counterexample
    is rather generic and can be applied to other primitives like encryption schemes.
    © 2011 International Association for Cryptologic Research.'
alternative_title:
- LNCS
author:
- first_name: Abhishek
  full_name: Jain, Abhishek
  last_name: Jain
- first_name: Krzysztof Z
  full_name: Krzysztof Pietrzak
  id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
  last_name: Pietrzak
  orcid: 0000-0002-9139-1654
citation:
  ama: 'Jain A, Pietrzak KZ. Parallel repetition for leakage resilience amplification
    revisited. In: Vol 6597. Springer; 2011:58-69. doi:<a href="https://doi.org/10.1007/978-3-642-19571-6_5">10.1007/978-3-642-19571-6_5</a>'
  apa: 'Jain, A., &#38; Pietrzak, K. Z. (2011). Parallel repetition for leakage resilience
    amplification revisited (Vol. 6597, pp. 58–69). Presented at the TCC: Theory of
    Cryptography Conference, Springer. <a href="https://doi.org/10.1007/978-3-642-19571-6_5">https://doi.org/10.1007/978-3-642-19571-6_5</a>'
  chicago: Jain, Abhishek, and Krzysztof Z Pietrzak. “Parallel Repetition for Leakage
    Resilience Amplification Revisited,” 6597:58–69. Springer, 2011. <a href="https://doi.org/10.1007/978-3-642-19571-6_5">https://doi.org/10.1007/978-3-642-19571-6_5</a>.
  ieee: 'A. Jain and K. Z. Pietrzak, “Parallel repetition for leakage resilience amplification
    revisited,” presented at the TCC: Theory of Cryptography Conference, 2011, vol.
    6597, pp. 58–69.'
  ista: 'Jain A, Pietrzak KZ. 2011. Parallel repetition for leakage resilience amplification
    revisited. TCC: Theory of Cryptography Conference, LNCS, vol. 6597, 58–69.'
  mla: Jain, Abhishek, and Krzysztof Z. Pietrzak. <i>Parallel Repetition for Leakage
    Resilience Amplification Revisited</i>. Vol. 6597, Springer, 2011, pp. 58–69,
    doi:<a href="https://doi.org/10.1007/978-3-642-19571-6_5">10.1007/978-3-642-19571-6_5</a>.
  short: A. Jain, K.Z. Pietrzak, in:, Springer, 2011, pp. 58–69.
conference:
  name: 'TCC: Theory of Cryptography Conference'
date_created: 2018-12-11T12:02:11Z
date_published: 2011-01-01T00:00:00Z
date_updated: 2021-01-12T07:42:00Z
day: '01'
doi: 10.1007/978-3-642-19571-6_5
extern: 1
month: '01'
page: 58 - 69
publication_status: published
publisher: Springer
publist_id: '3443'
quality_controlled: 0
status: public
title: Parallel repetition for leakage resilience amplification revisited
type: conference
volume: '6597 '
year: '2011'
...
