IMPRINTING AND X-CHROMOSOME COUNTING MECHANISMS DETERMINE XIST EXPRESSION IN EARLY MOUSE DEVELOPMENT

被引:209
作者
KAY, GF
BARTON, SC
SURANI, MA
RASTAN, S
机构
[1] MRC, CLIN RES CTR, COMPARAT BIOL SECT, HARROW HA1 3UJ, MIDDX, ENGLAND
[2] WELLCOME CANCER RES CAMPAIGN, INST CANC & DEV BIOL, CAMBRIDGE CB2 1QR, ENGLAND
[3] UNIV CAMBRIDGE, PHYSIOL LAB, CAMBRIDGE CB2 1QR, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0092-8674(94)90049-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mice, X inactivation is preceded by in cis Xist expression. Initially, normal female embryos express the paternal Xist allele exclusively, preceding imprinted X inactivation in the trophectoderm Later expression of Xist alleles is random, preceding random X inactivation in the epiblast lineage. In this study using uniparental embryos, we demonstrate that Xist expression is initially dictated solely by parental imprinting, causing expression of all paternal alleles. Maternal alleles remain repressed, irrespective of X chromosome number. At the compacting morula stage, this parental imprint is erased, and the mechanism counting the X chromosomes imposes appropriate Xist expression with respect to chromosome number. Our results also suggest that Xist expression may itself be regulated by a novel imprinted maternally expressed gene.
引用
收藏
页码:639 / 650
页数:12
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