Kay G F, Barton S C, Surani M A, Rastan S
Section of Comparative Biology, Medical Research Council Clinical Research Centre, Harrow, England.
Cell. 1994 Jun 3;77(5):639-50. doi: 10.1016/0092-8674(94)90049-3.
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.
在小鼠中,X染色体失活之前会发生顺式Xist基因表达。最初,正常雌性胚胎仅表达父本的Xist等位基因,这先于滋养外胚层中的印记X染色体失活。后来Xist等位基因的表达是随机的,先于上胚层谱系中的随机X染色体失活。在这项使用单亲胚胎的研究中,我们证明Xist基因的表达最初完全由亲本印记决定,导致所有父本等位基因的表达。母本等位基因保持沉默,与X染色体数量无关。在致密桑椹胚阶段,这种亲本印记被消除,计数X染色体的机制会根据染色体数量施加适当的Xist基因表达。我们的结果还表明,Xist基因的表达本身可能受一个新的母本印记表达基因调控。