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PMID: 9298902 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

X chromosome inactivation is mediated by Xist RNA stabilization.

Cell ·Vol. 90 ·No. 5 ·1997-09-05 ·Pages 907-16

Panning B, Dausman J, Jaenisch R

Abstract

Low level Xist expression can be detected from both active X chromosomes (Xa) in female embryonic stem cells prior to X inactivation. After differentiation, Xist is expressed at high levels only from the inactive X chromosome (Xi). Differentiating female cells increase Xist expression from the Xi prior to silencing low level Xist expression from the Xa. The transition from low level to high level expression is regulated by the stabilization of Xist transcripts at the Xi. We suggest that these developmentally modulated changes in Xist expression are regulated by several different mechanisms: factors that stabilize Xist transcripts at the Xi, an activity that blocks this stabilization at the Xa, and a mechanism that silences low level Xist expression from the Xa.

MeSH Terms
Animals Blastocyst/physiology Chromatin/physiology Dosage Compensation, Genetic Female Fibroblasts/cytology,physiology Gene Expression Regulation, Developmental/physiology Male Mice RNA Splicing/physiology RNA, Long Noncoding RNA, Messenger/metabolism RNA, Untranslated Stem Cells/cytology,physiology Transcription Factors/physiology Transcription, Genetic/physiology X Chromosome
Chemicals
Chromatin RNA, Long Noncoding RNA, Messenger RNA, Untranslated Transcription Factors XIST non-coding RNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Panning B
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA.
Dausman J
Jaenisch R
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1997-09-05
Pages
907-16
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · R35-CA44339 · United States
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