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Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems
The role of mechanical signals in cell identity determination remains poorly explored in tissues. Furthermore, because mechanical stress is widespread, mechanical signals are difficult to uncouple from biochemical-based transduction pathways. Here we focus on the homeobox gene SHOOT MERISTEMLESS (ST...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666715/ https://www.ncbi.nlm.nih.gov/pubmed/26623515 http://dx.doi.org/10.7554/eLife.07811 |
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author | Landrein, Benoît Kiss, Annamaria Sassi, Massimiliano Chauvet, Aurélie Das, Pradeep Cortizo, Millan Laufs, Patrick Takeda, Seiji Aida, Mitsuhiro Traas, Jan Vernoux, Teva Boudaoud, Arezki Hamant, Olivier |
author_facet | Landrein, Benoît Kiss, Annamaria Sassi, Massimiliano Chauvet, Aurélie Das, Pradeep Cortizo, Millan Laufs, Patrick Takeda, Seiji Aida, Mitsuhiro Traas, Jan Vernoux, Teva Boudaoud, Arezki Hamant, Olivier |
author_sort | Landrein, Benoît |
collection | PubMed |
description | The role of mechanical signals in cell identity determination remains poorly explored in tissues. Furthermore, because mechanical stress is widespread, mechanical signals are difficult to uncouple from biochemical-based transduction pathways. Here we focus on the homeobox gene SHOOT MERISTEMLESS (STM), a master regulator and marker of meristematic identity in Arabidopsis. We found that STM expression is quantitatively correlated to curvature in the saddle-shaped boundary domain of the shoot apical meristem. As tissue folding reflects the presence of mechanical stress, we test and demonstrate that STM expression is induced after micromechanical perturbations. We also show that STM expression in the boundary domain is required for organ separation. While STM expression correlates with auxin depletion in this domain, auxin distribution and STM expression can also be uncoupled. STM expression and boundary identity are thus strengthened through a synergy between auxin depletion and an auxin-independent mechanotransduction pathway at the shoot apical meristem. DOI: http://dx.doi.org/10.7554/eLife.07811.001 |
format | Online Article Text |
id | pubmed-4666715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46667152015-12-03 Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems Landrein, Benoît Kiss, Annamaria Sassi, Massimiliano Chauvet, Aurélie Das, Pradeep Cortizo, Millan Laufs, Patrick Takeda, Seiji Aida, Mitsuhiro Traas, Jan Vernoux, Teva Boudaoud, Arezki Hamant, Olivier eLife Developmental Biology and Stem Cells The role of mechanical signals in cell identity determination remains poorly explored in tissues. Furthermore, because mechanical stress is widespread, mechanical signals are difficult to uncouple from biochemical-based transduction pathways. Here we focus on the homeobox gene SHOOT MERISTEMLESS (STM), a master regulator and marker of meristematic identity in Arabidopsis. We found that STM expression is quantitatively correlated to curvature in the saddle-shaped boundary domain of the shoot apical meristem. As tissue folding reflects the presence of mechanical stress, we test and demonstrate that STM expression is induced after micromechanical perturbations. We also show that STM expression in the boundary domain is required for organ separation. While STM expression correlates with auxin depletion in this domain, auxin distribution and STM expression can also be uncoupled. STM expression and boundary identity are thus strengthened through a synergy between auxin depletion and an auxin-independent mechanotransduction pathway at the shoot apical meristem. DOI: http://dx.doi.org/10.7554/eLife.07811.001 eLife Sciences Publications, Ltd 2015-12-01 /pmc/articles/PMC4666715/ /pubmed/26623515 http://dx.doi.org/10.7554/eLife.07811 Text en © 2015, Landrein et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Landrein, Benoît Kiss, Annamaria Sassi, Massimiliano Chauvet, Aurélie Das, Pradeep Cortizo, Millan Laufs, Patrick Takeda, Seiji Aida, Mitsuhiro Traas, Jan Vernoux, Teva Boudaoud, Arezki Hamant, Olivier Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems |
title | Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems |
title_full | Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems |
title_fullStr | Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems |
title_full_unstemmed | Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems |
title_short | Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems |
title_sort | mechanical stress contributes to the expression of the stm homeobox gene in arabidopsis shoot meristems |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666715/ https://www.ncbi.nlm.nih.gov/pubmed/26623515 http://dx.doi.org/10.7554/eLife.07811 |
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