Genes that escape from X inactivation

被引:249
作者
Berletch, Joel B. [4 ]
Yang, Fan [4 ]
Xu, Jun [3 ]
Carrel, Laura [2 ]
Disteche, Christine M. [1 ,4 ]
机构
[1] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[2] Penn State Coll Med, Dept Biochem & Mol Biol, Hershey, PA 17033 USA
[3] Tufts Univ, Cummings Sch Vet Med, Dept Biomed Sci, North Grafton, MA 01536 USA
[4] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
MACROH2A1 HISTONE VARIANTS; HUMAN CELL-LINES; CHROMOSOME INACTIVATION; SEX-DIFFERENCES; DOSAGE COMPENSATION; TURNERS-SYNDROME; LINKED GENES; MOUSE-BRAIN; EXPRESSION; H3;
D O I
10.1007/s00439-011-1011-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To achieve a balanced gene expression dosage between males (XY) and females (XX), mammals have evolved a compensatory mechanism to randomly inactivate one of the female X chromosomes. Despite this chromosome-wide silencing, a number of genes escape X inactivation: in women about 15% of X-linked genes are bi-allelically expressed and in mice, about 3%. Expression from the inactive X allele varies from a few percent of that from the active allele to near equal expression. While most genes have a stable inactivation pattern, a subset of genes exhibit tissue-specific differences in escape from X inactivation. Escape genes appear to be protected from the repressive chromatin modifications associated with X inactivation. Differences in the identity and distribution of escape genes between species and tissues suggest a role for these genes in the evolution of sex differences in specific phenotypes. The higher expression of escape genes in females than in males implies that they may have female-specific roles and may be responsible for some of the phenotypes observed in X aneuploidy.
引用
收藏
页码:237 / 245
页数:9
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