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Description
  • DNA strand break repair by HR is mediated by genes of the RAD52 epistasis group. Rad52 protein plays central role in this process. It binds and anneals complementary ssDNA, self-associate to form multimeric rings, interacts with Rad51, and promotes nucleation of Rad51 onto ssDNA. Here, we show that Rad52 competes with Srs2 anti-recombinase in mediating Rad51-catalyzed strand exchange reaction through common interaction site on Rad51. The molecular mechanism of Rad52 function in homologous recombination together with the role of postranslational modification (SUMO-ylation) is discussed.
  • DNA strand break repair by HR is mediated by genes of the RAD52 epistasis group. Rad52 protein plays central role in this process. It binds and anneals complementary ssDNA, self-associate to form multimeric rings, interacts with Rad51, and promotes nucleation of Rad51 onto ssDNA. Here, we show that Rad52 competes with Srs2 anti-recombinase in mediating Rad51-catalyzed strand exchange reaction through common interaction site on Rad51. The molecular mechanism of Rad52 function in homologous recombination together with the role of postranslational modification (SUMO-ylation) is discussed. (en)
Title
  • Molecular dissection of Rad52 mediator activity
  • Molecular dissection of Rad52 mediator activity (en)
skos:prefLabel
  • Molecular dissection of Rad52 mediator activity
  • Molecular dissection of Rad52 mediator activity (en)
skos:notation
  • RIV/00216224:14310/07:00022863!RIV10-MSM-14310___
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  • P(LC06030), P(ME 888), Z(MSM0021622413)
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  • RIV/00216224:14310/07:00022863
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  • recombination; repair; cancer; Rad52; BRCA2 (en)
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  • [6F66AC60CF04]
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  • Heidelberg
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  • Krejčí, Lumír
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  • 14310
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