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


ABSTRACT: 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.

SUBMITTER: Rymen B 

PROVIDER: S-EPMC6828771 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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

Rymen Bart B   Kawamura Ayako A   Lambolez Alice A   Inagaki Soichi S   Takebayashi Arika A   Iwase Akira A   Sakamoto Yuki Y   Sako Kaori K   Favero David S DS   Ikeuchi Momoko M   Suzuki Takamasa T   Seki Motoaki M   Kakutani Tetsuji T   Roudier François F   Sugimoto Keiko K  

Communications biology 20191104


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 e  ...[more]

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