Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals

There is crosstalk between the maintenance of DNA methylation and histone methylation. Here, the authors create an Uhrf1 knockin mouse model that abolishes the H3K9me2/3-binding activity of Uhrf1, and show that DNA maintenance methylation in mammals is largely independent of H3K9 methylation.

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Autores principales: Qian Zhao, Jiqin Zhang, Ruoyu Chen, Lina Wang, Bo Li, Hao Cheng, Xiaoya Duan, Haijun Zhu, Wei Wei, Jiwen Li, Qihan Wu, Jing-Dong J. Han, Wenqiang Yu, Shaorong Gao, Guohong Li, Jiemin Wong
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Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/eaa46b60799b4bfabd64eeb76e38f5dd
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spelling oai:doaj.org-article:eaa46b60799b4bfabd64eeb76e38f5dd2021-12-02T14:39:12ZDissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals10.1038/ncomms124642041-1723https://doaj.org/article/eaa46b60799b4bfabd64eeb76e38f5dd2016-08-01T00:00:00Zhttps://doi.org/10.1038/ncomms12464https://doaj.org/toc/2041-1723There is crosstalk between the maintenance of DNA methylation and histone methylation. Here, the authors create an Uhrf1 knockin mouse model that abolishes the H3K9me2/3-binding activity of Uhrf1, and show that DNA maintenance methylation in mammals is largely independent of H3K9 methylation.Qian ZhaoJiqin ZhangRuoyu ChenLina WangBo LiHao ChengXiaoya DuanHaijun ZhuWei WeiJiwen LiQihan WuJing-Dong J. HanWenqiang YuShaorong GaoGuohong LiJiemin WongNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Qian Zhao
Jiqin Zhang
Ruoyu Chen
Lina Wang
Bo Li
Hao Cheng
Xiaoya Duan
Haijun Zhu
Wei Wei
Jiwen Li
Qihan Wu
Jing-Dong J. Han
Wenqiang Yu
Shaorong Gao
Guohong Li
Jiemin Wong
Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals
description There is crosstalk between the maintenance of DNA methylation and histone methylation. Here, the authors create an Uhrf1 knockin mouse model that abolishes the H3K9me2/3-binding activity of Uhrf1, and show that DNA maintenance methylation in mammals is largely independent of H3K9 methylation.
format article
author Qian Zhao
Jiqin Zhang
Ruoyu Chen
Lina Wang
Bo Li
Hao Cheng
Xiaoya Duan
Haijun Zhu
Wei Wei
Jiwen Li
Qihan Wu
Jing-Dong J. Han
Wenqiang Yu
Shaorong Gao
Guohong Li
Jiemin Wong
author_facet Qian Zhao
Jiqin Zhang
Ruoyu Chen
Lina Wang
Bo Li
Hao Cheng
Xiaoya Duan
Haijun Zhu
Wei Wei
Jiwen Li
Qihan Wu
Jing-Dong J. Han
Wenqiang Yu
Shaorong Gao
Guohong Li
Jiemin Wong
author_sort Qian Zhao
title Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals
title_short Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals
title_full Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals
title_fullStr Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals
title_full_unstemmed Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals
title_sort dissecting the precise role of h3k9 methylation in crosstalk with dna maintenance methylation in mammals
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/eaa46b60799b4bfabd64eeb76e38f5dd
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