Histone acetylation recruits the SWR1 complex to regulate active DNA demethylation in <i>Arabidopsis</i>

Wen‐Feng Nie(Chinese Academy of Sciences), Mingguang Lei(Chinese Academy of Sciences), Mingxuan Zhang(Chinese Academy of Sciences), Kai Tang(Chinese Academy of Sciences), Huan Huang(Chinese Academy of Sciences), Cuijun Zhang(Chinese Academy of Sciences), Daisuke Miki(Chinese Academy of Sciences), Pan Liu(Chinese Academy of Sciences), Yu Yang(Chinese Academy of Sciences), Xingang Wang(Purdue University West Lafayette), Heng Zhang(Chinese Academy of Sciences), Zhaobo Lang(Chinese Academy of Sciences), Na Liu, Xuechen Xu(Zhejiang University), Ramesh Yelagandula(Gregor Mendel Institute of Molecular Plant Biology), Huiming Zhang(Chinese Academy of Sciences), Zhidan Wang(Chinese Academy of Sciences), Xiaoqiang Chai(Chinese Academy of Sciences), Andrea Andreucci(University of Pisa), Jingquan Yu(Zhejiang University), Frédéric Berger(Gregor Mendel Institute of Molecular Plant Biology), Rosa Lozano‐Durán(Chinese Academy of Sciences), Jian‐Kang Zhu(Chinese Academy of Sciences)
Proceedings of the National Academy of Sciences
July 30, 2019
Cited by 131Open Access
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Abstract

Active DNA demethylation is critical for controlling the DNA methylomes in plants and mammals. However, little is known about how DNA demethylases are recruited to target loci, and the involvement of chromatin marks in this process. Here, we identify 2 components of the SWR1 chromatin-remodeling complex, PIE1 and ARP6, as required for ROS1-mediated DNA demethylation, and discover 2 SWR1-associated bromodomain-containing proteins, AtMBD9 and nuclear protein X1 (NPX1). AtMBD9 and NPX1 recognize histone acetylation marks established by increased DNA methylation 1 (IDM1), a known regulator of DNA demethylation, redundantly facilitating H2A.Z deposition at IDM1 target loci. We show that at some genomic regions, H2A.Z and DNA methylation marks coexist, and H2A.Z physically interacts with ROS1 to regulate DNA demethylation and antisilencing. Our results unveil a mechanism through which DNA demethylases can be recruited to specific target loci exhibiting particular histone marks, providing a conceptual framework to understand how chromatin marks regulate DNA demethylation.


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