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PMID: 8205614 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development.

Cell ·Vol. 77 ·No. 5 ·1994-06-03 ·Pages 639-50

Kay GF, Barton SC, Surani MA, Rastan S

Abstract

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.

Related Genes
MeSH Terms
Alleles Animals Dosage Compensation, Genetic Embryonic and Fetal Development/genetics Female Gene Expression Genes, Switch Male Mice Mice, Inbred C57BL Mice, Inbred CBA Parthenogenesis/genetics X Chromosome Y Chromosome
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kay G F
Section of Comparative Biology, Medical Research Council Clinical Research Centre, Harrow, England.
Barton S C
Surani M A
Rastan S
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1994-06-03
Pages
639-50
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
Wellcome Trust · United Kingdom
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