Article

  • The EMBO Journal (2004) 23, 4868 - 4875
  • doi:10.1038/sj.emboj.7600469

Published online: 18 November 2004

The CDK regulates repair of double-strand breaks by homologous recombination during the cell cycle

Yael Aylon, Batia Liefshitz and Martin Kupiec

  1. Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv, Israel

Correspondence to:

Martin Kupiec, Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv 69978, Israel. Tel.: +972 3 640 9031; Fax: +972 3 640 9407; E-mail: martin@post.tau.ac.il

Received 19 August 2004; Accepted 12 October 2004


DNA double-strand breaks (DSBs) are dangerous lesions that can lead to genomic instability and cell death. Eukaryotic cells repair DSBs either by nonhomologous end-joining (NHEJ) or by homologous recombination. We investigated the ability of yeast cells (Saccharomyces cerevisiae) to repair a single, chromosomal DSB by recombination at different stages of the cell cycle. We show that cells arrested at the G1 phase of the cell cycle restrict homologous recombination, but are able to repair the DSB by NHEJ. Furthermore, we demonstrate that recombination ability does not require duplicated chromatids or passage through S phase, and is controlled at the resection step by Clb–CDK activity.

  • Keywords:

    • checkpoint,
    • DNA repair,
    • DNA replication,
    • nonhomologous end-joining,
    • yeast
Top

MORE ARTICLES LIKE THIS

These links to content published by NPG are automatically generated

REVIEWS

Regulation of DNA repair throughout the cell cycle

Nature Reviews Molecular Cell Biology Review (01 Apr 2008)

See all 9 matches for Reviews

NEWS AND VIEWS

Telomeres on the Cdk roller-coaster ride

Nature Cell Biology News and Views (01 Jan 2007)