Biological function and regulation of histone and non-histone lysine   methylation in response to DNA damage

doi:10.1093/abbs/gmw050

CORC > 北京大学 > 生命科学学院

	Biological function and regulation of histone and non-histone lysine methylation in response to DNA damage
	Chen, Yongcan ; Zhu, Wei-Guo
刊名	ACTA BIOCHIMICA ET BIOPHYSICA SINICA
	2016
关键词	DNA damage response lysine methylation histone methylation DOUBLE-STRAND BREAKS HOMOLOGOUS RECOMBINATION REPAIR JMJD1C DEMETHYLATES MDC1 WOLF-HIRSCHHORN SYNDROME CHECKPOINT PROTEIN CRB2 CELL-CYCLE PROGRESSION END-JOINING REPAIR SACCHAROMYCES-CEREVISIAE TUMOR-SUPPRESSOR H3 METHYLATION
DOI	10.1093/abbs/gmw050
英文摘要	DNA damage response (DDR) signaling network is initiated to protect cells from various exogenous and endogenous damage resources. Timely and accurate regulation of DDR proteins is required for distinct DNA damage repair pathways. Post-translational modifications of histone and nonhistone proteins play a vital role in the DDR factor foci formation and signaling pathway. Phosphorylation, ubiquitylation, SUMOylation, neddylation, poly(ADP-ribosyl) ation, acetylation, and methylation are all involved in the spatial-temporal regulation of DDR, among which phosphorylation and ubiquitylation are well studied. Studies in the past decade also revealed extensive roles of lysine methylation in response to DNA damage. Lysine methylation is finely regulated by plenty of lysine methyltransferases, lysine demethylases, and can be recognized by proteins with chromodomain, plant homeodomain, Tudor domain, malignant brain tumor domain, or proline-tryptophan-tryptophan-proline domain. In this review, we outline the dynamics and regulation of histone lysine methylation at canonical (H3K4, H3K9, H3K27, H3K36, H3K79, and H4K20) and non-canonical sites after DNA damage, and discuss their context-specific functions in DDR protein recruitment or extraction, chromatin environment establishment, and transcriptional regulation. We also present the emerging advances of lysine methylation in non-histone proteins during DDR.; National Basic Research Program of China [2011CB910100, 2011CB504200, 2013CB911000]; National Natural Science Foundation of China [81222028, 81321003, 81472581, 81530074, 31570812, 91319302]; Ministry of Science and Technology of China [B70001]; SCI(E); PubMed; 中国科技核心期刊(ISTIC); REVIEW; zhuweiguo@bjmu.edu.cn; 7,SI; 603-616; 48
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/492038]
专题	生命科学学院
推荐引用方式 GB/T 7714	Chen, Yongcan,Zhu, Wei-Guo. Biological function and regulation of histone and non-histone lysine methylation in response to DNA damage[J]. ACTA BIOCHIMICA ET BIOPHYSICA SINICA,2016.
APA	Chen, Yongcan,&Zhu, Wei-Guo.(2016).Biological function and regulation of histone and non-histone lysine methylation in response to DNA damage.ACTA BIOCHIMICA ET BIOPHYSICA SINICA.
MLA	Chen, Yongcan,et al."Biological function and regulation of histone and non-histone lysine methylation in response to DNA damage".ACTA BIOCHIMICA ET BIOPHYSICA SINICA (2016).