IMR Press / FBL / Volume 3 / Issue 4 / DOI: 10.2741/A304

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article
DNA strand exchange proteins: a biochemical and physical comparison
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1 Sections of Microbiology and of Molecular and Cellular Biology, University of California, Davis, CA 95616
2 Microbiology Graduate Group, University of California, Davis, CA 95616
3 Norris Comprehensive Cancer Center, USC School of Medicine, 1441 Eastlake Ave., Los Angeles, CA 90033
Front. Biosci. (Landmark Ed) 1998, 3(4), 570–603; https://doi.org/10.2741/A304
Published: 17 June 1998
Abstract

Homologous genetic recombination is an essential biological process that involves the pairing and exchange of DNA between two homologous chromosomes or DNA molecules. It is of fundamental importance to the preservation of genomic integrity, the production of genetic diversity, and the proper segregation of chromosomes. In Escherichia coli, the RecA protein is essential to recombination, and biochemical analysis demonstrates that it is responsible for the crucial steps of homologous pairing and DNA strand exchange. The presence of RecA-like proteins, or their functional equivalents, in bacteriophage, other eubacteria, archaea, and eukaryotes, confirms that the mechanism of homologous pairing and DNA strand exchange is conserved throughout all forms of life. This review focuses on the biochemical and physical characteristics of DNA strand exchange proteins from three diverse organisms: RecA protein from E. coli, UvsX protein from Bacteriophage T4, and RAD51 protein from Saccharomyces cerevisiae.

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