Coordination of histone chaperones for parental histone segregation and epigenetic inheritance

被引:5
作者
Fang, Yimeng [1 ]
Hua, Xu [2 ,3 ,4 ]
Shan, Chun-Min [1 ,5 ]
Toda, Takenori [1 ]
Qiao, Feng [6 ]
Zhang, Zhiguo [2 ,3 ,4 ]
Jia, Songtao [1 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[2] Columbia Univ, Inst Canc Genet, Irving Med Ctr, New York, NY 10032 USA
[3] Columbia Univ, Dept Pediat, Irving Med Ctr, New York, NY 10032 USA
[4] Columbia Univ, Irving Med Ctr, Dept Genet & Dev, New York, NY 10032 USA
[5] Chinese Acad Sci, Inst Microbiol, State Key Lab Plant Genom, Beijing 100101, Peoples R China
[6] Univ Calif Irvine, Sch Med, Dept Biol Chem, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
heterochromatin; epigenetic inheritance; histone chaperone; Mcm2; Dpb3; Dpb4; eSPAN; fission yeast; parental histone density; SYMMETRIC INHERITANCE; LYSINE-9; METHYLATION; FISSION YEAST; HP1; PROTEINS; HETEROCHROMATIN; DNA; CHROMATIN; COMPLEX; MAINTENANCE; H3-H4;
D O I
10.1101/gad.351278.123
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In this study, Fang et al. report that the helicase subunit MCM2, DNA polymerase epsilon subunits DPB3/4, and histone chaperone FACT complex function collectively to maintain symmetrical parental histone segregation during heterochromatin replication in yeast. They further reveal a basis for leading/lagging strand bias of heterochromatin inheritance and describe the distinct dependence of inheritance efficiency on histone density, providing new insight into the mechanisms of inheritable epigenetic memory. Chromatin-based epigenetic memory relies on the accurate distribution of parental histone H3-H4 tetramers to newly replicated DNA strands. Mcm2, a subunit of the replicative helicase, and Dpb3/4, subunits of DNA polymerase epsilon, govern parental histone H3-H4 deposition to the lagging and leading strands, respectively. However, their contribution to epigenetic inheritance remains controversial. Here, using fission yeast heterochromatin inheritance systems that eliminate interference from initiation pathways, we show that a Mcm2 histone binding mutation severely disrupts heterochromatin inheritance, while mutations in Dpb3/4 cause only moderate defects. Surprisingly, simultaneous mutations of Mcm2 and Dpb3/4 stabilize heterochromatin inheritance. eSPAN (enrichment and sequencing of protein-associated nascent DNA) analyses confirmed the conservation of Mcm2 and Dpb3/4 functions in parental histone H3-H4 segregation, with their combined absence showing a more symmetric distribution of parental histone H3-H4 than either single mutation alone. Furthermore, the FACT histone chaperone regulates parental histone transfer to both strands and collaborates with Mcm2 and Dpb3/4 to maintain parental histone H3-H4 density and faithful heterochromatin inheritance. These results underscore the importance of both symmetric distribution of parental histones and their density at daughter strands for epigenetic inheritance and unveil distinctive properties of parental histone chaperones during DNA replication.
引用
收藏
页码:189 / 204
页数:16
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