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PMID: 2554135 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

DNA topoisomerases and models of sister-chromatid exchange.

Mutation research ·Vol. 215 ·No. 1 ·1989-11-00 ·Pages 15-23

Dillehay LE, Jacobson-Kram D, Williams JR

Abstract

Pommier et al. (1985) suggested that sister-chromatid exchange (SCE) results from exchange of topoisomerase II subunits. "Homologous displacement", an alternative mechanism, is proposed in which strand switching occurs during removal of parental helical turns by topoisomerases. The steps in the SCE model proposed by Ishii and Bender (1980) for SCE occurring at a blocked replication fork could occur by this mechanism and would require the action of both topoisomerases I and II. Homologous displacement involving topoisomerase II alone provides a mechanism for the strand switching required in the models of Kato (1977) and Cleaver (1981) in which SCE occur between replicated double strands. These mechanisms and models are discussed in relation to current knowledge of the locations and functions of topoisomerases during DNA replication.

MeSH Terms
DNA Replication DNA Topoisomerases, Type I/metabolism DNA Topoisomerases, Type II/metabolism Models, Genetic Replicon Sister Chromatid Exchange
Chemicals
DNA Topoisomerases, Type I DNA Topoisomerases, Type II
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dillehay L E
Radiobiology Laboratory, Johns Hopkins Oncology Center, Baltimore, MD 21205.
Jacobson-Kram D
Williams J R
Article Info
Journal
Mutation research
Abbr.
Mutat Res
ISSN
0027-5107
Published
1989-11-00
Pages
15-23
Language
English
Region
Netherlands
NLM ID
0400763
Subset
IM
Grants
NCI NIH HHS · CA39543 · United States
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