4.7 Article

APOBEC3A can activate the DNA damage response and cause cell-cycle arrest

期刊

EMBO REPORTS
卷 12, 期 5, 页码 444-450

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/embor.2011.46

关键词

APOBEC3A; cytidine deaminase; DNA damage; uracil-DNA glycosylase

资金

  1. Pioneer Developmental Chair from the Salk Institute
  2. National Institutes of Health [AI067952, AI074967]
  3. Instituto de Salud 'Carlos III'/Consejo Superior de Investigaciones Cientificas/Salk Institute
  4. Lynn Streim Postdoctoral Endowment Fellowship
  5. Natural Sciences & Engineering Research Council of Canada

向作者/读者索取更多资源

Human apolipoprotein-B mRNA-editing catalytic polypeptide-like 3 (APOBEC3) proteins constitute a family of cytidine deaminases that mediate restriction of retroviruses, endogenous retro-elements and DNA viruses. It is well established that these enzymes are potent mutators of viral DNA, but it is unclear whether their editing activity is a threat to the integrity of the cellular genome. We show that expression of APOBEC3A can lead to induction of DNA breaks and activation of damage responses in a deaminase-dependent manner. Consistent with these observations, APOBEC3A expression induces cell-cycle arrest. These results indicate that cellular DNA is vulnerable to APOBEC3 activity and deregulated expression of APOBEC3A could threaten genomic integrity.

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