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PMID: 2009864 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Double-strand-break repair and recombination catalyzed by a nuclear extract of Saccharomyces cerevisiae.

The EMBO journal ·Vol. 10 ·No. 4 ·1991-04-00 ·Pages 987-96

Symington LS

Abstract

An in vitro system for double-strand-break repair and recombination of plasmid substrates catalyzed by extracts prepared from yeast nuclei has been developed. Recombination events that generate crossover products were detected amongst reaction products by Southern blot hybridization, or by the polymerase chain reaction (PCR). The recombination reaction was found to be stimulated by a double-strand break within homologous sequences and proceeded by a mechanism that involved branched DNA intermediates. In addition to pairing events that generate crossovers, the formation of inverted repeats (head-to-head and tail-to-tail joined products) was also detected. Two models are presented which propose that the formation of crossover products and inverted repeats occur by similar mechanisms.

MeSH Terms
Base Sequence Blotting, Southern Cell Nucleus/metabolism Cloning, Molecular Crossing Over, Genetic DNA Damage DNA Repair Escherichia coli/genetics Models, Genetic Molecular Sequence Data Nucleic Acid Hybridization Oligonucleotide Probes Plasmids Polymerase Chain Reaction Recombination, Genetic Restriction Mapping Saccharomyces cerevisiae/genetics,metabolism
Chemicals
Oligonucleotide Probes
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Symington L S
Institute of Cancer Research, Columbia University College of Physicians and Surgeons, New York, NY 10032.
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1991-04-00
Pages
987-96
Language
English
Region
England
NLM ID
8208664
PMCID
PMC452743
Subset
IM
Grants
NIGMS NIH HHS · R01 GM041784 · United States
NIGMS NIH HHS · GM41784 · United States
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