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PMID: 21478274 Published · ppublish English

Structure of a CENP-A-histone H4 heterodimer in complex with chaperone HJURP.

Genes & development ·Vol. 25 ·No. 9 ·2011-06-24

Hu Hao, Liu Yang, Wang Mingzhu, Fang Junnan, Huang Hongda, Yang Na, Li Yanbo, Wang Jianyu, Yao Xuebiao, Shi Yunyu, Li Guohong, Xu Rui-Ming

Abstract

In higher eukaryotes, the centromere is epigenetically specified by the histone H3 variant Centromere Protein-A (CENP-A). Deposition of CENP-A to the centromere requires histone chaperone HJURP (Holliday junction recognition protein). The crystal structure of an HJURP-CENP-A-histone H4 complex shows that HJURP binds a CENP-A-H4 heterodimer. The C-terminal β-sheet domain of HJURP caps the DNA-binding region of the histone heterodimer, preventing it from spontaneous association with DNA. Our analysis also revealed a novel site in CENP-A that distinguishes it from histone H3 in its ability to bind HJURP. These findings provide key information for specific recognition of CENP-A and mechanistic insights into the process of centromeric chromatin assembly.

Article Info
Journal
Genes & development
Abbr.
Genes Dev
Published
2011-06-24
Indexed
2011-05-03
Updated
2016-10-25
Language
English
Country/Region
United States
NLM ID
8711660
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