Dense Chromatin Activates Polycomb Repressive Complex 2 to Regulate H3 Lysine 27 Methylation

Author:

Yuan Wen12,Wu Tong12,Fu Hang12,Dai Chao3,Wu Hui24,Liu Nan25,Li Xiang24,Xu Mo24,Zhang Zhuqiang2,Niu Tianhui12,Han Zhifu2,Chai Jijie26,Zhou Xianghong Jasmine3,Gao Shaorong2,Zhu Bing2

Affiliation:

1. College of Biological Sciences, China Agricultural University, Beijing 100094, China.

2. National Institute of Biological Sciences, Beijing 102206, China.

3. Program in Molecular and Computational Biology, University of Southern California, Los Angeles, CA 90089, USA.

4. Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.

5. Beijing Normal University, Beijing 100875, China.

6. Tsinghua University, Beijing 10084, China.

Abstract

Maintaining Repression The Polycomb Repressive Complex 2 (PRC2) plays a critical role in gene silencing in metazoans, methylating histone H3 on lysine 27 (H3K27) to generate a repressive chromatin mark. The catalytic subunit E(z)/Ezh2 requires the presence of two other subunits—ESC/EED and Su(z)12—for enzyme activity. Yuan et al. (p. 971 ; see the Perspective by Pirrotta ) show that both a fragment of the histone H3 N-terminal tail, and histone H1 stimulated PRC2 enzyme activity on poor, low-density chromatin substrates, indicating that that PRC2 is regulated by the density and compaction states of chromatin. The histone H3 fragment binds to the Su(z)12 subunit of PRC2 to stimulate E(z)/Ezh2. Local chromatin compaction preceded establishment of histone H3K27 methylation indicating how PRC2 might maintain the repressed state.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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