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pubmed-article:7536936pubmed:abstractTextDuring early mammalian embryogenesis, one of the two X chromosomes in somatic cells of the female becomes inactivated through a process that is thought to depend on a unique initiator region, the X-chromosome inactivation center (Xic). The recently characterized Xist sequence (X-inactive-specific transcript) is thought to be a possible candidate for Xic. In mice a further genetic element, the X chromosome-controlling element (Xce), is also known to influence the choice of which of the two X chromosomes is inactivated. We report that a region of the mouse X chromosome lying 15 kb distal to Xist contains several sites that show hypermethylation specifically associated with the active X chromosome. Analysis of this region in various Xce strains has revealed a correlation between the strength of the Xce allele carried and the methylation status of this region. We propose that such a region could be involved in the initial stages of the inactivation process and in particular in the choice of which of the two X chromosomes present in a female cell will be inactivated.lld:pubmed
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pubmed-article:7536936pubmed:articleTitleXce haplotypes show modified methylation in a region of the active X chromosome lying 3' to Xist.lld:pubmed
pubmed-article:7536936pubmed:affiliationUnité de Génétique Moléculaire Murine, Institut Pasteur, Paris, France.lld:pubmed
pubmed-article:7536936pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7536936pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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