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Plant stem cell maintenance involves direct transcriptional repression of differentiation program
In animal systems, master regulatory transcription factors (TFs) mediate stem cell maintenance through a direct transcriptional repression of differentiation promoting TFs. Whether similar mechanisms operate in plants is not known. In plants, shoot apical meristems serve as reservoirs of stem cells...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658276/ https://www.ncbi.nlm.nih.gov/pubmed/23549482 http://dx.doi.org/10.1038/msb.2013.8 |
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author | Yadav, Ram Kishor Perales, Mariano Gruel, Jérémy Ohno, Carolyn Heisler, Marcus Girke, Thomas Jönsson, Henrik Reddy, G Venugopala |
author_facet | Yadav, Ram Kishor Perales, Mariano Gruel, Jérémy Ohno, Carolyn Heisler, Marcus Girke, Thomas Jönsson, Henrik Reddy, G Venugopala |
author_sort | Yadav, Ram Kishor |
collection | PubMed |
description | In animal systems, master regulatory transcription factors (TFs) mediate stem cell maintenance through a direct transcriptional repression of differentiation promoting TFs. Whether similar mechanisms operate in plants is not known. In plants, shoot apical meristems serve as reservoirs of stem cells that provide cells for all above ground organs. WUSCHEL, a homeodomain TF produced in cells of the niche, migrates into adjacent cells where it specifies stem cells. Through high-resolution genomic analysis, we show that WUSCHEL represses a large number of genes that are expressed in differentiating cells including a group of differentiation promoting TFs involved in leaf development. We show that WUS directly binds to the regulatory regions of differentiation promoting TFs; KANADI1, KANADI2, ASYMMETRICLEAVES2 and YABBY3 to repress their expression. Predictions from a computational model, supported by live imaging, reveal that WUS-mediated repression prevents premature differentiation of stem cell progenitors, being part of a minimal regulatory network for meristem maintenance. Our work shows that direct transcriptional repression of differentiation promoting TFs is an evolutionarily conserved logic for stem cell regulation. |
format | Online Article Text |
id | pubmed-3658276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-36582762013-05-20 Plant stem cell maintenance involves direct transcriptional repression of differentiation program Yadav, Ram Kishor Perales, Mariano Gruel, Jérémy Ohno, Carolyn Heisler, Marcus Girke, Thomas Jönsson, Henrik Reddy, G Venugopala Mol Syst Biol Article In animal systems, master regulatory transcription factors (TFs) mediate stem cell maintenance through a direct transcriptional repression of differentiation promoting TFs. Whether similar mechanisms operate in plants is not known. In plants, shoot apical meristems serve as reservoirs of stem cells that provide cells for all above ground organs. WUSCHEL, a homeodomain TF produced in cells of the niche, migrates into adjacent cells where it specifies stem cells. Through high-resolution genomic analysis, we show that WUSCHEL represses a large number of genes that are expressed in differentiating cells including a group of differentiation promoting TFs involved in leaf development. We show that WUS directly binds to the regulatory regions of differentiation promoting TFs; KANADI1, KANADI2, ASYMMETRICLEAVES2 and YABBY3 to repress their expression. Predictions from a computational model, supported by live imaging, reveal that WUS-mediated repression prevents premature differentiation of stem cell progenitors, being part of a minimal regulatory network for meristem maintenance. Our work shows that direct transcriptional repression of differentiation promoting TFs is an evolutionarily conserved logic for stem cell regulation. European Molecular Biology Organization 2013-04-02 /pmc/articles/PMC3658276/ /pubmed/23549482 http://dx.doi.org/10.1038/msb.2013.8 Text en Copyright © 2013, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by/3.0/This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Article Yadav, Ram Kishor Perales, Mariano Gruel, Jérémy Ohno, Carolyn Heisler, Marcus Girke, Thomas Jönsson, Henrik Reddy, G Venugopala Plant stem cell maintenance involves direct transcriptional repression of differentiation program |
title | Plant stem cell maintenance involves direct transcriptional repression of differentiation program |
title_full | Plant stem cell maintenance involves direct transcriptional repression of differentiation program |
title_fullStr | Plant stem cell maintenance involves direct transcriptional repression of differentiation program |
title_full_unstemmed | Plant stem cell maintenance involves direct transcriptional repression of differentiation program |
title_short | Plant stem cell maintenance involves direct transcriptional repression of differentiation program |
title_sort | plant stem cell maintenance involves direct transcriptional repression of differentiation program |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658276/ https://www.ncbi.nlm.nih.gov/pubmed/23549482 http://dx.doi.org/10.1038/msb.2013.8 |
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