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Homologous Recombination
Chapter 10 Homologous Recombination 25 and 27 September, 2006
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Overview Homologous recombination relies on regions of nearly identical sequence. The Holliday model of the mechanism of recombination involves recognition, strand invasion, branch migration, and resolution. The Double-strand Break Repair model is similar, but involves two Holliday junctions. Homologous recombination is mediated by protein enzymes. RecA (Rad51p) pairs homologous regions and promotes strand exchange. RecBCD (Rad 50/58/60p; MRXp) generates single strand for invasion. RuvAB and RuvC (?) promote branch migration and resolution. Homologous recombination is required for successful meiosis. In meiosis, Spo11 generates DSB, MRXp extends the break, and Rad51 promotes strand invasion. Some events, including mating-type switching in yeast and VDJ recombination involve regulated, specific recombination.
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Holliday Junction Cleavage and Strand Invasion
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Holliday Resolution
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DSB Recombination
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DNA Damage leads to DSB
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RecBCD and Chi Sites
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Chi Site Polarity
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RecA-catalyzed Strand Exchange
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RecA - DNA Structures
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Polarity of Cooperative RecA Binding
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Mechanism of RecA Strand Exchange
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RuvAB and Branch Migration
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RuvC Resolves Holliday Structures
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Meiotic Recombination
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Spo11p forms Double-stranded Breaks
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Recombination Mechanism
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Mating-Type Conversion
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The mechanism of mating-type conversion involves replication to bring about gene conversion.
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Genetic and Physical Maps
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Gene Conversion by Mismatch Repair
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Resolving Paired Holliday Structures
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