AI Article Synopsis

  • Telomeres protect chromosome ends from degradation and disruptions, but the specific mechanisms behind this protection are not completely understood.
  • In budding yeast, the Cdc13 protein is crucial for telomere capping, and defective capping occurs in certain mutants, especially at high temperatures.
  • The study shows that stabilizing G-quadruplex (G4) DNA through various treatments can compensate for cdc13-1 capping issues, highlighting G4 DNA's potential protective role at telomeres even when normal capping is absent.

Article Abstract

Telomere capping conceals chromosome ends from exonucleases and checkpoints, but the full range of capping mechanisms is not well defined. Telomeres have the potential to form G-quadruplex (G4) DNA, although evidence for telomere G4 DNA function in vivo is limited. In budding yeast, capping requires the Cdc13 protein and is lost at nonpermissive temperatures in cdc13-1 mutants. Here, we use several independent G4 DNA-stabilizing treatments to suppress cdc13-1 capping defects. These include overexpression of three different G4 DNA binding proteins, loss of the G4 DNA unwinding helicase Sgs1, or treatment with small molecule G4 DNA ligands. In vitro, we show that protein-bound G4 DNA at a 3' overhang inhibits 5'→3' resection of a paired strand by exonuclease I. These findings demonstrate that, at least in the absence of full natural capping, G4 DNA can play a positive role at telomeres in vivo.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119813PMC
http://dx.doi.org/10.1038/nsmb.2033DOI Listing

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