HP1 Heterochromatin binding proteins working the genome

被引:112
作者
Zeng, Weihua [1 ]
Ball, Alexander R., Jr. [1 ]
Yokomori, Kyoko [1 ]
机构
[1] Univ Calif Irvine, Dept Biol Chem, Sch Med, Irvine, CA 92717 USA
关键词
HP1; gamma; cohesin; DNA repair; transcription; heterochromatin; D4Z4; FSHD; H3K9me3; DOUBLE-STRAND BREAKS; HISTONE H3; LYSINE-9; METHYLATION; CELL-CYCLE; RECRUITMENT; COHESIN; REPAIR; METHYLTRANSFERASE; CENTROMERES; ROLES;
D O I
10.4161/epi.5.4.11683
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
Heterochromatin Protein 1 (HP1) is a transcriptional repressor that directly binds to the methylated lysine 9 residue of histone H3 (H3K9me), which is a hallmark histone modification for transcriptionally silenced heterochromatin. Studies of homologs in different organisms have provided significant insight into the function of HP1 and the role of H3K9me. Initially discovered to be a major constituent of heterochromatin important for gene silencing, HP1 is now known to be a dynamic protein that also functions in transcriptional elongation, centromeric sister chromatid cohesion, telomere maintenance and DNA repair. Furthermore, recent studies have begun to uncover functional differences between HP1 variants and their H3K9me-independent mode of action. As our understanding of HP1 expands, however, conflicting data has also been reported that requires further reconciliation. Here we focus on some of the recent findings and controversies concerning HP1 functions in mammalian cells in comparison to studies in other organisms.
引用
收藏
页码:287 / 292
页数:6
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