Mathematical modeling of histone modifications reveals the formation mechanism and function of bivalent chromatin

被引:12
作者
Zhao, Wei [1 ,2 ]
Qiao, Lingxia [1 ]
Yan, Shiyu [2 ]
Nie, Qing [3 ,4 ]
Zhang, Lei [1 ,2 ]
机构
[1] Peking Univ, Beijing Int Ctr Math Res, Beijing 100871, Peoples R China
[2] Peking Univ, Ctr Quantitat Biol, Beijing 100871, Peoples R China
[3] Univ Calif Irvine, Dept Math, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
基金
中国国家自然科学基金;
关键词
MINIMUM ACTION METHOD; TARGET GENES; METHYLATION; H3K27ME3; H3; RECRUITMENT; SIGNATURES; DOMAINS; EZH2; DNA;
D O I
10.1016/j.isci.2021.102732
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bivalent chromatin is characterized by occupation of both activating and repressive histone modifications. Here, we develop a mathematical model that involves antagonistic histone modifications H3K4me3 and H3K27me3 to capture the key features of bivalent chromatin. Three necessary conditions for the emergence of bivalent chromatin are identified, including advantageous methylating activity over demethylating activity, frequent noise conversions of modifications, and sufficient nonlinearity. The first condition is further confirmed by analyzing the existing experimental data. Investigation of the composition of bivalent chromatin reveals that bivalent nucleosomes carrying both H3K4me3 and H3K27me3 account for no more than half of nucleosomes at the bivalent chromatin domain. We identify that bivalent chromatin not only allows transitions to multiple states but also serves as a stepping stone to facilitate a stepwise transition between repressive chromatin state and activating chromatin state and thus elucidate crucial roles of bivalent chromatin in mediating phenotypical plasticity during cell fate determination.
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页数:18
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