Homozygous Tsix mutant mice reveal a sex-ratio distortion and revert to random X-inactivation

被引:63
作者
Lee, JT [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Mol Biol, Howard Hughes Med Inst, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ng939
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tsix(1) controls X-chromosome inactivation (XCI) by blocking the accumulation of Xist(2-4) RNA on the future active X chromosome(5-7). Deleting Tsix on one X chromosome ((XX)-X-Delta) skews XCI toward the mutated X chromosome in the female soma. Here 1 have generated homozygous Tsix-null mice ((XXDelta)-X-Delta) to test how deleting the second allele affects the choice of XCI. Homozygosity leads to extremely low fertility and reveals two previously unknown non-mendelian patterns of inheritance. First, the sex ratio is skewed against female births so that one daughter is born for every two to three sons: Second, the pattern of XCI unexpectedly returns to random in surviving (XXDelta)-X-Delta mice. Thus, with respect to choice, mutation of Tsix yields a phenotypic abnormality in heterozygotes but not homozygotes. To reconcile the paradox of female loss with apparent reversion to random choice, I propose that deleting both Tsix alleles results In chaotic choice and that randomness in (XXDelta)-X-Delta survivors reflects a fortuitous selection of distinct X chromosomes as active and inactive.
引用
收藏
页码:195 / 200
页数:6
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