Noncoding RNAs and Epigenetic Mechanisms During X-Chromosome Inactivation

被引:138
作者
Gendrel, Anne-Valerie [1 ]
Heard, Edith [1 ]
机构
[1] Inst Curie, Mammalian Dev Epigenet Grp, Genet & Dev Biol Unit, F-75248 Paris, France
来源
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 30 | 2014年 / 30卷
关键词
Xist; chromatin; dosage compensation; monoallelic expression; EMBRYONIC STEM-CELLS; PROTEIN-CODING GENE; XIST-RNA; DOSAGE COMPENSATION; REPEAT HYPOTHESIS; MOUSE DEVELOPMENT; DNA METHYLATION; LINKED GENES; IN-VIVO; SAF-A;
D O I
10.1146/annurev-cellbio-101512-122415
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In mammals, the process of X-chromosome inactivation ensures equivalent levels of X-linked gene expression between males and females through the silencing of one of the two X chromosomes in female cells. The process is established early in development and is initiated by a unique locus, which produces a long noncoding RNA, Xist. The Xist transcript triggers gene silencing in cis by coating the future inactive X chromosome. It also induces a cascade of chromatin changes, including posttranslational histone modifications and DNA methylation, and leads to the stable repression of all X-linked genes throughout development and adult life. We review here recent progress in our understanding of the molecular mechanisms involved in the initiation of Xist expression, the propagation of the Xist RNA along the chromosome, and the cis-elements and trans-acting factors involved in the maintenance of the repressed state. We also describe the diverse strategies used by nonplacental mammals for X-chromosome dosage compensation and highlight the common features and differences between eutherians and metatherians, in particular regarding the involvement of long noncoding RNAs.
引用
收藏
页码:561 / 580
页数:20
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