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Histone chaperones in nucleosome assembly and human disease
被引:279
|作者:
Burgess, Rebecca J.
[1
]
Zhang, Zhiguo
[1
]
机构:
[1] Mayo Clin, Coll Med, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
基金:
美国国家科学基金会;
美国国家卫生研究院;
关键词:
SYNDROME CANDIDATE GENE;
DNA-REPLICATION;
STRUCTURAL BASIS;
CENP-A;
CHROMATIN REPLICATION;
H3-H4;
TETRAMERS;
H3;
EXCHANGE;
VARIANT;
ACETYLATION;
PROTEIN;
D O I:
10.1038/nsmb.2461
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Nucleosome assembly following DNA replication, DNA repair and gene transcription is critical for the maintenance of genome stability and epigenetic information. Nucleosomes are assembled by replication-coupled or replication-independent pathways with the aid of histone chaperone proteins. How these different nucleosome assembly pathways are regulated remains relatively unclear. Recent studies have provided insight into the mechanisms and the roles of histone chaperones in regulating nucleosome assembly. Alterations or mutations in factors involved in nucleosome assembly have also been implicated in cancer and other human diseases. This review highlights the recent progress and outlines future challenges in the field.
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页码:14 / 22
页数:9
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