Cargando…

Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation

Trichome patterning in Arabidopsis serves as a model system to study how single cells are selected within a field of initially equivalent cells. Current models explain this pattern by an activator–inhibitor feedback loop. Here, we report that also a newly discovered mechanism is involved by which pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Bouyer, Daniel, Geier, Florian, Kragler, Friedrich, Schnittger, Arp, Pesch, Martina, Wester, Katja, Balkunde, Rachappa, Timmer, Jens, Fleck, Christian, Hülskamp, Martin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2422854/
https://www.ncbi.nlm.nih.gov/pubmed/18547143
http://dx.doi.org/10.1371/journal.pbio.0060141
_version_ 1782156081584144384
author Bouyer, Daniel
Geier, Florian
Kragler, Friedrich
Schnittger, Arp
Pesch, Martina
Wester, Katja
Balkunde, Rachappa
Timmer, Jens
Fleck, Christian
Hülskamp, Martin
author_facet Bouyer, Daniel
Geier, Florian
Kragler, Friedrich
Schnittger, Arp
Pesch, Martina
Wester, Katja
Balkunde, Rachappa
Timmer, Jens
Fleck, Christian
Hülskamp, Martin
author_sort Bouyer, Daniel
collection PubMed
description Trichome patterning in Arabidopsis serves as a model system to study how single cells are selected within a field of initially equivalent cells. Current models explain this pattern by an activator–inhibitor feedback loop. Here, we report that also a newly discovered mechanism is involved by which patterning is governed by the removal of the trichome-promoting factor TRANSPARENT TESTA GLABRA1 (TTG1) from non-trichome cells. We demonstrate by clonal analysis and misexpression studies that Arabidopsis TTG1 can act non-cell-autonomously and by microinjection experiments that TTG1 protein moves between cells. While TTG1 is expressed ubiquitously, TTG1–YFP protein accumulates in trichomes and is depleted in the surrounding cells. TTG1–YFP depletion depends on GLABRA3 (GL3), suggesting that the depletion is governed by a trapping mechanism. To study the potential of the observed trapping/depletion mechanism, we formulated a mathematical model enabling us to evaluate the relevance of each parameter and to identify parameters explaining the paradoxical genetic finding that strong ttg1 alleles are glabrous, while weak alleles exhibit trichome clusters.
format Text
id pubmed-2422854
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-24228542008-06-10 Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation Bouyer, Daniel Geier, Florian Kragler, Friedrich Schnittger, Arp Pesch, Martina Wester, Katja Balkunde, Rachappa Timmer, Jens Fleck, Christian Hülskamp, Martin PLoS Biol Research Article Trichome patterning in Arabidopsis serves as a model system to study how single cells are selected within a field of initially equivalent cells. Current models explain this pattern by an activator–inhibitor feedback loop. Here, we report that also a newly discovered mechanism is involved by which patterning is governed by the removal of the trichome-promoting factor TRANSPARENT TESTA GLABRA1 (TTG1) from non-trichome cells. We demonstrate by clonal analysis and misexpression studies that Arabidopsis TTG1 can act non-cell-autonomously and by microinjection experiments that TTG1 protein moves between cells. While TTG1 is expressed ubiquitously, TTG1–YFP protein accumulates in trichomes and is depleted in the surrounding cells. TTG1–YFP depletion depends on GLABRA3 (GL3), suggesting that the depletion is governed by a trapping mechanism. To study the potential of the observed trapping/depletion mechanism, we formulated a mathematical model enabling us to evaluate the relevance of each parameter and to identify parameters explaining the paradoxical genetic finding that strong ttg1 alleles are glabrous, while weak alleles exhibit trichome clusters. Public Library of Science 2008-06 2008-06-10 /pmc/articles/PMC2422854/ /pubmed/18547143 http://dx.doi.org/10.1371/journal.pbio.0060141 Text en © 2008 Bouyer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bouyer, Daniel
Geier, Florian
Kragler, Friedrich
Schnittger, Arp
Pesch, Martina
Wester, Katja
Balkunde, Rachappa
Timmer, Jens
Fleck, Christian
Hülskamp, Martin
Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation
title Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation
title_full Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation
title_fullStr Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation
title_full_unstemmed Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation
title_short Two-Dimensional Patterning by a Trapping/Depletion Mechanism: The Role of TTG1 and GL3 in Arabidopsis Trichome Formation
title_sort two-dimensional patterning by a trapping/depletion mechanism: the role of ttg1 and gl3 in arabidopsis trichome formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2422854/
https://www.ncbi.nlm.nih.gov/pubmed/18547143
http://dx.doi.org/10.1371/journal.pbio.0060141
work_keys_str_mv AT bouyerdaniel twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT geierflorian twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT kraglerfriedrich twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT schnittgerarp twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT peschmartina twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT westerkatja twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT balkunderachappa twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT timmerjens twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT fleckchristian twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation
AT hulskampmartin twodimensionalpatterningbyatrappingdepletionmechanismtheroleofttg1andgl3inarabidopsistrichomeformation