Partitioning of Histone H3-H4 Tetramers During DNA Replication-Dependent Chromatin Assembly

被引:263
|
作者
Xu, Mo [1 ,2 ,3 ]
Long, Chengzu [1 ]
Chen, Xiuzhen [1 ,4 ]
Huang, Chang [1 ,5 ]
Chen, She [1 ]
Zhu, Bing [1 ]
机构
[1] Natl Inst Biol Sci, Beijing 102206, Peoples R China
[2] Peking Union Med Coll, Grad Program, Beijing 100730, Peoples R China
[3] Chinese Acad Med Sci, Beijing 100730, Peoples R China
[4] Beijing Normal Univ, Life Sci Coll, Beijing 100875, Peoples R China
[5] China Agr Univ, Coll Biol Sci, Dept Biochem, Beijing 100094, Peoples R China
关键词
NEWLY SYNTHESIZED HISTONES; HYBRID NUCLEOSOMES; H3; SEGREGATION; DEPOSITION; H4; METHYLATION; PATHWAYS;
D O I
10.1126/science.1178994
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
Semiconservative DNA replication ensures the faithful duplication of genetic information during cell divisions. However, how epigenetic information carried by histone modifications propagates through mitotic divisions remains elusive. To address this question, the DNA replication-dependent nucleosome partition pattern must be clarified. Here, we report significant amounts of H3.3-H4 tetramers split in vivo, whereas most H3.1-H4 tetramers remained intact. Inhibiting DNA replication-dependent deposition greatly reduced the level of splitting events, which suggests that (i) the replication-independent H3.3 deposition pathway proceeds largely by cooperatively incorporating two new H3.3-H4 dimers and (ii) the majority of splitting events occurred during replication-dependent deposition. Our results support the idea that "silent" histone modifications within large heterochromatic regions are maintained by copying modifications from neighboring preexisting histones without the need for H3-H4 splitting events.
引用
收藏
页码:94 / 98
页数:5
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