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DNA End Resection: Nucleases Team Up with the Right Partners to Initiate Homologous Recombination

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 290, Issue 38, Pages 22931-22938

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.R115.675942

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Funding

  1. Swiss National Science Foundation [PP00P3 133636]
  2. Swiss National Science Foundation (SNF) [PP00P3_133636] Funding Source: Swiss National Science Foundation (SNF)

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The repair of DNA double-strand breaks by homologous recombination commences by nucleolytic degradation of the 5'-terminated strand of the DNA break. This leads to the formation of 3'-tailed DNA, which serves as a substrate for the strand exchange protein Rad51. The nucleoprotein filament then invades homologous DNA to drive template-directed repair. In this review, I discuss mainly the mechanisms of DNA end resection in Saccharomyces cerevisiae, which includes short-range resection by Mre11-Rad50-Xrs2 and Sae2, as well as processive long-range resection by Sgs1-Dna2 or Exo1 pathways. Resection mechanisms are highly conserved between yeast and humans, and analogous machineries are found in prokaryotes as well.

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