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Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS

Specification of new organs from transit amplifying cells is critical for higher eukaryote development. In plants, a central stem cell pool maintained by the pluripotency factor SHOOTMERISTEMLESS (STM), is surrounded by transit amplifying cells competent to respond to auxin hormone maxima by giving...

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Autores principales: Chung, Yuhee, Zhu, Yang, Wu, Miin-Feng, Simonini, Sara, Kuhn, Andre, Armenta-Medina, Alma, Jin, Run, Østergaard, Lars, Gillmor, C. Stewart, Wagner, Doris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385194/
https://www.ncbi.nlm.nih.gov/pubmed/30792395
http://dx.doi.org/10.1038/s41467-019-08861-3
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author Chung, Yuhee
Zhu, Yang
Wu, Miin-Feng
Simonini, Sara
Kuhn, Andre
Armenta-Medina, Alma
Jin, Run
Østergaard, Lars
Gillmor, C. Stewart
Wagner, Doris
author_facet Chung, Yuhee
Zhu, Yang
Wu, Miin-Feng
Simonini, Sara
Kuhn, Andre
Armenta-Medina, Alma
Jin, Run
Østergaard, Lars
Gillmor, C. Stewart
Wagner, Doris
author_sort Chung, Yuhee
collection PubMed
description Specification of new organs from transit amplifying cells is critical for higher eukaryote development. In plants, a central stem cell pool maintained by the pluripotency factor SHOOTMERISTEMLESS (STM), is surrounded by transit amplifying cells competent to respond to auxin hormone maxima by giving rise to new organs. Auxin triggers flower initiation through Auxin Response Factor (ARF) MONOPTEROS (MP) and recruitment of chromatin remodelers to activate genes promoting floral fate. The contribution of gene repression to reproductive primordium initiation is poorly understood. Here we show that downregulation of the STM pluripotency gene promotes initiation of flowers and uncover the mechanism for STM silencing. The ARFs ETTIN (ETT) and ARF4 promote organogenesis at the reproductive shoot apex in parallel with MP via histone-deacetylation mediated transcriptional silencing of STM. ETT and ARF4 directly repress STM, while MP acts indirectly, through its target FILAMENTOUS FLOWER (FIL). Our data suggest that – as in animals- downregulation of the pluripotency program is important for organogenesis in plants.
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spelling pubmed-63851942019-02-25 Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS Chung, Yuhee Zhu, Yang Wu, Miin-Feng Simonini, Sara Kuhn, Andre Armenta-Medina, Alma Jin, Run Østergaard, Lars Gillmor, C. Stewart Wagner, Doris Nat Commun Article Specification of new organs from transit amplifying cells is critical for higher eukaryote development. In plants, a central stem cell pool maintained by the pluripotency factor SHOOTMERISTEMLESS (STM), is surrounded by transit amplifying cells competent to respond to auxin hormone maxima by giving rise to new organs. Auxin triggers flower initiation through Auxin Response Factor (ARF) MONOPTEROS (MP) and recruitment of chromatin remodelers to activate genes promoting floral fate. The contribution of gene repression to reproductive primordium initiation is poorly understood. Here we show that downregulation of the STM pluripotency gene promotes initiation of flowers and uncover the mechanism for STM silencing. The ARFs ETTIN (ETT) and ARF4 promote organogenesis at the reproductive shoot apex in parallel with MP via histone-deacetylation mediated transcriptional silencing of STM. ETT and ARF4 directly repress STM, while MP acts indirectly, through its target FILAMENTOUS FLOWER (FIL). Our data suggest that – as in animals- downregulation of the pluripotency program is important for organogenesis in plants. Nature Publishing Group UK 2019-02-21 /pmc/articles/PMC6385194/ /pubmed/30792395 http://dx.doi.org/10.1038/s41467-019-08861-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chung, Yuhee
Zhu, Yang
Wu, Miin-Feng
Simonini, Sara
Kuhn, Andre
Armenta-Medina, Alma
Jin, Run
Østergaard, Lars
Gillmor, C. Stewart
Wagner, Doris
Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS
title Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS
title_full Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS
title_fullStr Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS
title_full_unstemmed Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS
title_short Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS
title_sort auxin response factors promote organogenesis by chromatin-mediated repression of the pluripotency gene shootmeristemless
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385194/
https://www.ncbi.nlm.nih.gov/pubmed/30792395
http://dx.doi.org/10.1038/s41467-019-08861-3
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