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DNA Repair (Amst). 2010 Dec 10;9(12):1241-8. doi: 10.1016/j.dnarep.2010.09.016.

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

Author information

1
Life Sciences Institute, Zhejiang University, Hangzhou, Zhejiang 310058, China.

Abstract

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 RAD18 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.

PMID:
20971043
DOI:
10.1016/j.dnarep.2010.09.016
[Indexed for MEDLINE]

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