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

Author:

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.

Publisher

Cold Spring Harbor Laboratory

Subject

Developmental Biology,Genetics

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