Human x inactivation center induces random X chromosome inactivation in male transgenic mice

被引:47
作者
Migeon, BR
Kazi, E
Haisley-Royster, C
Hu, J
Reeves, R
Call, L
Lawler, A
Moore, CS
Morrison, H
Jeppesen, P
机构
[1] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Dept Physiol, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Sch Med, Dept Obstet & Gynecol, Baltimore, MD 21287 USA
[5] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
D O I
10.1006/geno.1999.5861
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
X chromosome inactivation is the means to down-regulate the transcriptional output of X chromosomes in female mammals. Essential DNA from the murine X inactivation center (Xic) has been identified by introducing it into male embryonic stem (ES) cells. To identify the essential sequences on human X chromosomes, we transfected male mouse ES cells with a YAC transgene containing 480 kb of the putative human X inactivation center (XIC). Despite little DNA sequence conservation, the human transgene is recognized as a second Xic in these XY mouse cells and induces random inactivation in chimeric mice derived from these cells. Inactivation is extensive on the X chromosome, but more localized on chromosome 11 carrying the transgene, demonstrating that initial inactivation and spreading of inactivation signals along the chromosome are independent events. Our results show for the first time that the DNA included in the human XIC transgene is sufficient to initiate random X inactivation, even in cells of another species. Interspecies XIC trangenes should facilitate further investigation of this process in humans and other mammals. (C) 1999 Academic Press.
引用
收藏
页码:113 / 121
页数:9
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