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PMID: 1345169 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Expression of Xist in mouse germ cells correlates with X-chromosome inactivation.

Nature genetics ·Vol. 2 ·No. 3 ·1992-11-00 ·Pages 200-3

McCarrey JR, Dilworth DD

Abstract

Mammals compensate for different doses of X-chromosome-linked genes in male (XY) and female (XX) somatic cells by terminally inactivating all but one X chromosome in each cell. A transiently inactive X chromosome is also found in germ cells, specifically in premeiotic oogenic cells and in meiotic and postmeiotic spermatogenic cells. Here we show that the Xist gene, which is a expressed predominantly from the inactive X-chromosome in female somatic cells, is also expressed in germ cells of both sexes, but only at those stages when an inactive X chromosome is present. This suggests support for the putative role of Xist as a regulator of X-chromosome inactivation and suggest a common mechanism for the initiation and/or maintenance of X-chromosome inactivation in all cell types.

MeSH Terms
Animals Base Sequence DNA, Complementary Dosage Compensation, Genetic Female Gene Expression/genetics Germ Cells/metabolism Liver/metabolism Male Meiosis/genetics Mice Molecular Sequence Data Ovum/metabolism,physiology RNA, Long Noncoding RNA, Messenger/analysis,biosynthesis RNA, Untranslated Spermatozoa/metabolism,physiology Testis/metabolism,physiology Transcription Factors/genetics Transcription, Genetic X Chromosome
Chemicals
DNA, Complementary RNA, Long Noncoding RNA, Messenger RNA, Untranslated Transcription Factors XIST non-coding RNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
McCarrey J R
Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, TX 78228.
Dilworth D D
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1992-11-00
Pages
200-3
Language
English
Region
United States
NLM ID
9216904
Subset
IM
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