
doi: 10.1007/bf01924006
pmid: 8143797
Homologous recombination occurs at higher than average frequency at and near hotspots. Hotspots are special nucleotide sequences recognized by proteins that promote, directly or indirectly, a rate limiting step of recombination. This review focuses on two well-studied examples, the Chi sites of the bacterium Escherichia coli and the M26 site of the fission yeast Schizosaccharomyces pombe. Chi, 5' G-C-T-G-G-T-G-G 3', is recognized by the RecBCD enzyme, which nicks the DNA near Chi and produces a 3'-ended single-stranded DNA 'tail'; this tail is a potent substrate for homologous pairing by RecA and single-stranded DNA binding proteins. M26, 5' A-T-G-A-C-G-T 3', is recognized by a heterodimeric protein and stimulates, by an as-yet-unknown mechanism, meiotic recombination at and near the ade6 gene. Additional hotspots in bacteria, fungi, and mammals enhance recombination directly or indirectly via a variety of mechanisms. Although hotspots are widespread among organisms, the biological role of their localized enhancement of recombination remains a matter of speculation.
Recombination, Genetic, Binding Sites, Exodeoxyribonuclease V, Exodeoxyribonucleases, Schizosaccharomyces, Escherichia coli, Regulatory Sequences, Nucleic Acid
Recombination, Genetic, Binding Sites, Exodeoxyribonuclease V, Exodeoxyribonucleases, Schizosaccharomyces, Escherichia coli, Regulatory Sequences, Nucleic Acid
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