DNA resection in eukaryotes: deciding how to fix the break.

Nat Struct Mol Biol

The Wellcome Trust and Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, UK.

Published: January 2010

AI Article Synopsis

  • DNA double-strand breaks (DSBs) can be repaired mainly through mechanisms like homologous recombination and nonhomologous end-joining.
  • DNA-end resection is a crucial first step in the recombination process, generating single-stranded DNA and affecting the choice of DSB repair.
  • Recent research highlights the mechanisms and regulation of resection in eukaryotes, discussing the implications of its failure or deregulation on recombination and potential human diseases.

Article Abstract

DNA double-strand breaks are repaired by different mechanisms, including homologous recombination and nonhomologous end-joining. DNA-end resection, the first step in recombination, is a key step that contributes to the choice of DSB repair. Resection, an evolutionarily conserved process that generates single-stranded DNA, is linked to checkpoint activation and is critical for survival. Failure to regulate and execute this process results in defective recombination and can contribute to human disease. Here I review recent findings on the mechanisms of resection in eukaryotes, from yeast to vertebrates, provide insights into the regulatory strategies that control it, and highlight the consequences of both its impairment and its deregulation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850169PMC
http://dx.doi.org/10.1038/nsmb.1710DOI Listing

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