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PMID: 1998141 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

DNA methylation of two X chromosome genes in female somatic and embryonal carcinoma cells.

Somatic cell and molecular genetics ·Vol. 17 ·No. 1 ·1991-01-00 ·Pages 35-47

Bartlett MH, Adra CN, Park J, Chapman VM, McBurney MW

Abstract

The extent of methylation of DNA sequences upstream and within the two X-linked genes, Pgk-1 and Hprt, was analyzed in male and female somatic cells and in female embryonal carcinoma cells carrying either two active X chromosomes (Xa) or one active and one inactive X chromosome (Xi). Sites upstream and within the first intron of both Pgk-1 and Hprt were heavily methylated on the Xi in somatic cells and in embryonal carcinoma cells with an Xi. Reactivation of this Xi was accompanied by extensive demethylation of these sites. In female embryonal carcinoma cells with two active X chromosomes, one X inactivates during differentiation in culture; however, methylation did not occur during differentiation, consistent with the idea that DNA methylation does not play a role in the initiation of X inactivation but may be involved in maintaining inactivation of those genes on the Xi.

Related Genes
MeSH Terms
Animals Blotting, Southern Cell Line Dosage Compensation, Genetic Female Gene Expression Regulation, Enzymologic Genes Hypoxanthine Phosphoribosyltransferase/genetics Kidney/physiology Male Methylation Mice Phosphoglycerate Kinase/genetics Promoter Regions, Genetic Restriction Mapping Spleen/physiology X Chromosome
Chemicals
Hypoxanthine Phosphoribosyltransferase Phosphoglycerate Kinase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Bartlett M H
Department of Medicine, University of Ottawa, Ontario, Canada.
Adra C N
Park J
Chapman V M
McBurney M W
Article Info
Journal
Somatic cell and molecular genetics
Abbr.
Somat Cell Mol Genet
ISSN
0740-7750
Published
1991-01-00
Pages
35-47
Language
English
Region
United States
NLM ID
8403568
Subset
IM
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