X chromosome reactivation in reprogramming and in development

被引:42
|
作者
Pasque, Vincent [1 ]
Plath, Kathrin [1 ]
机构
[1] Univ Calif Los Angeles, Dept Biol Chem, Eli & Edythe Broad,Ctr Regenerat Med & Stem Cell, Jonsson Comprehens Canc Ctr,David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
EMBRYONIC STEM-CELLS; GROUND-STATE PLURIPOTENCY; PRIMORDIAL GERM-CELLS; EARLY MOUSE EMBRYOS; XIST RNA; DOSAGE COMPENSATION; INACTIVATION CENTER; DNA METHYLATION; SOMATIC-CELLS; IPS CELLS;
D O I
10.1016/j.ceb.2015.10.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dramatic epigenetic changes take place during mammalian differentiation from the naive pluripotent state including the silencing of one of the two X chromosomes in female cells through X chromosome inactivation. Conversely, reprogramming of somatic cells to naive pluripotency is coupled to X chromosome reactivation (XCR). Recent studies in the mouse system have shed light on the mechanisms of XCR by uncovering the timing and steps of XCR during reprogramming to induced pluripotent stem cells (iPSCs), allowing the generation of testable hypotheses during embryogenesis. In contrast, analyses of the X chromosome in human iPSCs have revealed important differences between mouse and human reprogramming processes that can partially be explained by the establishment of distinct pluripotent states and impact disease modeling and the application of human pluripotent stem cells. Here, we review recent literature on XCR as a readout and determinant of reprogramming to pluripotency.
引用
收藏
页码:75 / 83
页数:9
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