reviewAnnual Review of GeneticsMar 2, 2011Closed access

Double-Strand Break End Resection and Repair Pathway Choice

Columbia University Irving Medical Center · Cancer Genetics (United States)

PubMed
Indexed incrossrefpubmed

Abstract

DNA double-strand breaks (DSBs) are cytotoxic lesions that can result in mutagenic events or cell death if left unrepaired or repaired inappropriately. Cells use two major pathways for DSB repair: nonhomologous end joining (NHEJ) and homologous recombination (HR). The choice between these pathways depends on the phase of the cell cycle and the nature of the DSB ends. A critical determinant of repair pathway choice is the initiation of 5'-3' resection of DNA ends, which commits cells to homology-dependent repair, and prevents repair by classical NHEJ. Here, we review the components of the end resection machinery, the role of end structure, and the cell-cycle phase on resection and the interplay of end…

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1,507
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Authors

2

Topics & keywords

Keywords
  • Non-homologous end joining
  • Homologous recombination
  • Biology
  • Homology directed repair
  • DNA repair
  • Cell cycle
  • DNA damage
  • Cell biology
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