Genetic and pharmacological reactivation of the mammalian inactive X chromosome

被引:56
作者
Bhatnagar, Sanchita [1 ,2 ,3 ]
Zhu, Xiaochun [1 ,2 ,3 ]
Ou, Jianhong [2 ,3 ]
Lin, Ling [1 ,2 ,3 ]
Chamberlain, Lynn [1 ,2 ,3 ]
Zhu, Lihua J. [2 ,3 ,4 ]
Wajapeyee, Narendra [5 ]
Green, Michael R. [1 ,2 ,3 ]
机构
[1] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[3] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[4] Univ Massachusetts, Sch Med, Program Bioinformat & Integrat Biol, Worcester, MA 01605 USA
[5] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
MECP2; RNA FISH; RNA-seq; RETT-SYNDROME; XIST RNA; DOSAGE COMPENSATION; MOUSE; METHYLATION; MECP2; CELLS; HYBRIDIZATION; RECRUITMENT; MAINTENANCE;
D O I
10.1073/pnas.1413620111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
X-chromosome inactivation (XCI), the random transcriptional silencing of one X chromosome in somatic cells of female mammals, is a mechanism that ensures equal expression of X-linked genes in both sexes. XCI is initiated in cis by the noncoding Xist RNA, which coats the inactive X chromosome (Xi) from which it is produced. However, trans-acting factors that mediate XCI remain largely unknown. Here, we perform a large-scale RNA interference screen to identify trans-acting XCI factors (XCIFs) that comprise regulators of cell signaling and transcription, including the DNA methyltransferase, DNMT1. The expression pattern of the XCIFs explains the selective onset of XCI following differentiation. The XCIFs function, at least in part, by promoting expression and/or localization of Xist to the Xi. Surprisingly, we find that DNMT1, which is generally a transcriptional repressor, is an activator of Xist transcription. Small-molecule inhibitors of two of the XCIFs can reversibly reactivate the Xi, which has implications for treatment of Rett syndrome and other dominant X-linked diseases. A homozygous mouse knockout of one of the XCIFs, stanniocalcin 1 (STC1), has an expected XCI defect but surprisingly is phenotypically normal. Remarkably, X-linked genes are not overexpressed in female Stc1(-/-) mice, revealing the existence of a mechanism(s) that can compensate for a persistent XCI deficiency to regulate X-linked gene expression.
引用
收藏
页码:12591 / 12598
页数:8
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