X chromosome regulation: diverse patterns in development, tissues and disease

被引:222
作者
Deng, Xinxian [1 ]
Berletch, Joel B. [1 ]
Nguyen, Di K. [1 ]
Disteche, Christine M. [1 ,2 ]
机构
[1] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Med, Seattle, WA 98115 USA
基金
美国国家卫生研究院;
关键词
LONG NONCODING RNAS; DOSAGE-COMPENSATION; INACTIVE X; SEX-DIFFERENCES; LINKED GENES; MAMMALIAN X; DNA METHYLATION; UP-REGULATION; XIST RNA; MOUSE;
D O I
10.1038/nrg3687
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genes on the mammalian X chromosome are present in one copy in mates and two copies in females. The complex mechanisms that regulate the X chromosome lead to evolutionary and physiological variability in gene expression between species, the sexes, individuals, developmental stages, tissues and cell types. In early development, delayed and incomplete X chromosome inactivation (XCI) in some species causes variability in gene expression. Additional diversity stems from escape from XCI and from mosaicism or XCI skewing in females. This causes sex-specific differences that manifest as differential gene expression and associated phenotypes. Furthermore, the complexity and diversity of X dosage regulation affect the severity of diseases caused by X-linked mutations.
引用
收藏
页码:367 / 378
页数:12
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