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Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis

Plant somatic cells reprogram and regenerate new tissues or organs when they are severely damaged. These physiological processes are associated with dynamic transcriptional responses but how chromatin-based regulation contributes to wound-induced gene expression changes and subsequent cellular repro...

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Autores principales: Rymen, Bart, Kawamura, Ayako, Lambolez, Alice, Inagaki, Soichi, Takebayashi, Arika, Iwase, Akira, Sakamoto, Yuki, Sako, Kaori, Favero, David S., Ikeuchi, Momoko, Suzuki, Takamasa, Seki, Motoaki, Kakutani, Tetsuji, Roudier, François, Sugimoto, Keiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828771/
https://www.ncbi.nlm.nih.gov/pubmed/31701032
http://dx.doi.org/10.1038/s42003-019-0646-5
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author Rymen, Bart
Kawamura, Ayako
Lambolez, Alice
Inagaki, Soichi
Takebayashi, Arika
Iwase, Akira
Sakamoto, Yuki
Sako, Kaori
Favero, David S.
Ikeuchi, Momoko
Suzuki, Takamasa
Seki, Motoaki
Kakutani, Tetsuji
Roudier, François
Sugimoto, Keiko
author_facet Rymen, Bart
Kawamura, Ayako
Lambolez, Alice
Inagaki, Soichi
Takebayashi, Arika
Iwase, Akira
Sakamoto, Yuki
Sako, Kaori
Favero, David S.
Ikeuchi, Momoko
Suzuki, Takamasa
Seki, Motoaki
Kakutani, Tetsuji
Roudier, François
Sugimoto, Keiko
author_sort Rymen, Bart
collection PubMed
description Plant somatic cells reprogram and regenerate new tissues or organs when they are severely damaged. These physiological processes are associated with dynamic transcriptional responses but how chromatin-based regulation contributes to wound-induced gene expression changes and subsequent cellular reprogramming remains unknown. In this study we investigate the temporal dynamics of the histone modifications H3K9/14ac, H3K27ac, H3K4me3, H3K27me3, and H3K36me3, and analyze their correlation with gene expression at early time points after wounding. We show that a majority of the few thousand genes rapidly induced by wounding are marked with H3K9/14ac and H3K27ac before and/or shortly after wounding, and these include key wound-inducible reprogramming genes such as WIND1, ERF113/RAP2.6 L and LBD16. Our data further demonstrate that inhibition of GNAT-MYST-mediated histone acetylation strongly blocks wound-induced transcriptional activation as well as callus formation at wound sites. This study thus uncovered a key epigenetic mechanism that underlies wound-induced cellular reprogramming in plants.
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spelling pubmed-68287712019-11-07 Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis Rymen, Bart Kawamura, Ayako Lambolez, Alice Inagaki, Soichi Takebayashi, Arika Iwase, Akira Sakamoto, Yuki Sako, Kaori Favero, David S. Ikeuchi, Momoko Suzuki, Takamasa Seki, Motoaki Kakutani, Tetsuji Roudier, François Sugimoto, Keiko Commun Biol Article Plant somatic cells reprogram and regenerate new tissues or organs when they are severely damaged. These physiological processes are associated with dynamic transcriptional responses but how chromatin-based regulation contributes to wound-induced gene expression changes and subsequent cellular reprogramming remains unknown. In this study we investigate the temporal dynamics of the histone modifications H3K9/14ac, H3K27ac, H3K4me3, H3K27me3, and H3K36me3, and analyze their correlation with gene expression at early time points after wounding. We show that a majority of the few thousand genes rapidly induced by wounding are marked with H3K9/14ac and H3K27ac before and/or shortly after wounding, and these include key wound-inducible reprogramming genes such as WIND1, ERF113/RAP2.6 L and LBD16. Our data further demonstrate that inhibition of GNAT-MYST-mediated histone acetylation strongly blocks wound-induced transcriptional activation as well as callus formation at wound sites. This study thus uncovered a key epigenetic mechanism that underlies wound-induced cellular reprogramming in plants. Nature Publishing Group UK 2019-11-04 /pmc/articles/PMC6828771/ /pubmed/31701032 http://dx.doi.org/10.1038/s42003-019-0646-5 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
Rymen, Bart
Kawamura, Ayako
Lambolez, Alice
Inagaki, Soichi
Takebayashi, Arika
Iwase, Akira
Sakamoto, Yuki
Sako, Kaori
Favero, David S.
Ikeuchi, Momoko
Suzuki, Takamasa
Seki, Motoaki
Kakutani, Tetsuji
Roudier, François
Sugimoto, Keiko
Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis
title Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis
title_full Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis
title_fullStr Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis
title_full_unstemmed Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis
title_short Histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in Arabidopsis
title_sort histone acetylation orchestrates wound-induced transcriptional activation and cellular reprogramming in arabidopsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828771/
https://www.ncbi.nlm.nih.gov/pubmed/31701032
http://dx.doi.org/10.1038/s42003-019-0646-5
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