Getting down to the core of histone modifications

被引:8
作者
Jack, Antonia P. M. [1 ]
Hake, Sandra B. [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Mol Biol, Adolf Butenandt Inst, D-80366 Munich, Germany
[2] Ctr Integrated Prot Sci Munich CIPSM, Munich, Germany
关键词
Chromatin; H3K56; H3K64; H3K79; H3T118; H3K122; Nucleosome; Transcription; Enhancer; RNA-POLYMERASE-II; LYSINE; 56; ACETYLATION; H3K79; METHYLATION; TRANSCRIPTIONAL ELONGATION; H3K56; CELL-CYCLE; TELOMERIC HETEROCHROMATIN; NUCLEAR PERIPHERY; STRUCTURAL BASIS; MAMMALIAN-CELLS;
D O I
10.1007/s00412-014-0465-x
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
The identification of an increasing number of posttranslationally modified residues within histone core domains is furthering our understanding of how nucleosome dynamics are regulated. In this review, we first discuss how the targeting of specific histone H3 core residues can directly influence the nucleosome structure and then apply this knowledge to provide functional reasoning for their localization to distinct genomic regions. While we focus mainly on transcriptional implications, the principles discussed in this review can also be applied to their roles in other cellular processes. Finally, we highlight some examples of how aberrant modifications of core histone residues can facilitate the pathogenesis of some diseases.
引用
收藏
页码:355 / 371
页数:17
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