The MORC family New epigenetic regulators of transcription and DNA damage response

被引:77
作者
Li, Da-Qiang [1 ]
Nair, Sujit S. [1 ,2 ]
Kumar, Rakesh [1 ,2 ]
机构
[1] George Washington Univ, Sch Med & Hlth Sci, Dept Biochem & Mol Med, Washington, DC 20052 USA
[2] George Washington Univ, Sch Med & Hlth Sci, McCormick Genom & Prote Ctr, Washington, DC 20052 USA
基金
美国国家卫生研究院;
关键词
MORC; chromatin remodeling; epigenetic regulation; transcription; DNA damage response; COILED-COIL DOMAIN; CHROMOSOMES-HINGE DOMAIN; LEUKEMIA NUCLEAR-BODIES; STRAND BREAK REPAIR; CHROMATIN-REMODELING COMPLEXES; PROTEIN-PROTEIN INTERACTIONS; CW DOMAIN; HOMOLOGOUS RECOMBINATION; HISTONE DEMETHYLASE; DISEASE RESISTANCE;
D O I
10.4161/epi.24976
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
Microrchidia (MORC) is a highly conserved nuclear protein superfamily with widespread domain architectures that intimately link MORCs with signaling-dependent chromatin remodeling and epigenetic regulation. Accumulating structural and biochemical evidence has shed new light on the mechanistic action and emerging role of MORCs as epigenetic regulators in diverse nuclear processes. In this Point of View, we focus on discussing recent advances in our understanding of the unique domain architectures of MORC family of chromatin remodelers and their potential contribution to epigenetic control of DNA template-dependent processes such as transcription and DNA damage response. Given that the deregulation of MORCs has been linked with human cancer and other diseases, further efforts to uncover the structure and function of MORCs may ultimately lead to the development of new approaches to intersect with the functionality of MORC family of chromatin remodeling proteins to correct associated pathogenesis.
引用
收藏
页码:685 / 693
页数:9
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