Sex chromosome inactivation in germ cells: emerging roles of DNA damage response pathways

被引:61
作者
Ichijima, Yosuke [1 ]
Sin, Ho-Su [1 ]
Namekawa, Satoshi H. [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Pediat,Perinatal Inst, Cincinnati Childrens Hosp Med Ctr,Div Reprod Sci, Cincinnati, OH 45221 USA
关键词
Germ cells; Meiosis; Sex chromosomes; DNA damage response; Checkpoint; Epigenetics; DOUBLE-STRAND BREAKS; XY BODY; UNSYNAPSED CHROMATIN; PACHYTENE CHECKPOINT; MEIOTIC CHROMOSOMES; SOMATIC-CELLS; CROSSING-OVER; MOUSE; BRCA1; MDC1;
D O I
10.1007/s00018-012-0941-5
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
Sex chromosome inactivation in male germ cells is a paradigm of epigenetic programming during sexual reproduction. Recent progress has revealed the underlying mechanisms of sex chromosome inactivation in male meiosis. The trigger of chromosome-wide silencing is activation of the DNA damage response (DDR) pathway, which is centered on the mediator of DNA damage checkpoint 1 (MDC1), a binding partner of phosphorylated histone H2AX (gamma H2AX). This DDR pathway shares features with the somatic DDR pathway recognizing DNA replication stress in the S phase. Additionally, it is likely to be distinct from the DDR pathway that recognizes meiosis-specific double-strand breaks. This review article extensively discusses the underlying mechanism of sex chromosome inactivation.
引用
收藏
页码:2559 / 2572
页数:14
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