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RAD18 lives a double life: Its implication in DNA double-strand break repair

期刊

DNA REPAIR
卷 9, 期 12, 页码 1241-1248

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.dnarep.2010.09.016

关键词

RAD18; Post-replication repair (PRR); Homologous recombination (HR); Checkpoint

资金

  1. Life Sciences Institute, ZJU
  2. Fundamental Research Funds for the Central Universities
  3. National Institutes of Health
  4. Department of Defense [W81XWH-05-1-0470]
  5. M.D. Anderson Cancer Center [CA016672]

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Maintenance of genome stability depends on efficient and accurate repair of DNA lesions. Failure to properly repair damaged DNA can cause cell death, mutations and chromosomal instability, which eventually lead to tumorigenesis. The E3 ligase RAD18 is well-known for its function in DNA damage bypass and post-replication repair (PRR) in yeast and vertebrates via its ability to facilitate PCNA mono-ubiquitination at stalled replication forks. However, emerging evidence has also indicated that RAM 8 plays an important role in homologous recombination (HR) in mammalian cells, which is an error-free DNA repair pathway that mediates the repair of double-strand breaks (DSBs). Here, we review how RAD18 carries out these distinct functions in response to different types of DNA lesions. (C) 2010 Elsevier E.V. All rights reserved.

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