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PMID: 2339112 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Asynchronous replication of homologous loci on human active and inactive X chromosomes.

Schmidt M, Migeon BR

Abstract

The two X chromosomes in mammalian females replicate asynchronously, the inactive later than the active one. Using BrdUrd-sensitive restriction and UV irradiation to identify newly synthesized DNA directly on Southern blots, and restriction fragment length differences to discriminate alleles on active and inactive human X chromosomes, we examined the replication of hypoxanthine phosphoribosyltransferase (HPRT) and clotting factor IX (F9) loci in clonal populations of mouse-human hybrids. We find that HPRT replicates at different times during the period of DNA synthesis (S phase), depending on its activity: It replicates in early S phase, when expressed (on the active X chromosome), and in late S phase when silent (on the inactive X chromosome). Furthermore, when reactivated, the derepressed locus is earlier replicating, supporting a relationship between replication and transcription. Neither F9 allele is expressed in these cells, and both replicate in the second half of S phase, (slightly earlier on active than on inactive X chromosome).

MeSH Terms
Alleles Animals Blotting, Southern Bromodeoxyuridine Cell Line DNA/genetics,isolation & purification DNA Probes DNA Replication Female Humans Hybrid Cells/cytology Hypoxanthine Phosphoribosyltransferase/genetics Interphase Mice Mitosis Restriction Mapping X Chromosome
Chemicals
DNA Probes DNA Hypoxanthine Phosphoribosyltransferase Bromodeoxyuridine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Schmidt M
Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Migeon B R
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28 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1990-05-00
Pages
3685-9
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC53967
Subset
IM
Grants
NICHD NIH HHS · HD 05465 · United States
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