Regulation of WRN protein cellular localization and enzymatic activities by SIRT1-mediated deacetylation
Graduate School of Biomedical Sciences; Department of Cancer Biology and the Cancer Center
Life Sciences | Medicine and Health Sciences
Werner syndrome is an autosomal recessive disorder associated with premature aging and cancer predisposition caused by mutations of the WRN gene. WRN is a member of the RecQ DNA helicase family with functions in maintaining genome stability. Sir2, an NAD-dependent histone deacetylase, has been proven to extend life span in yeast and Caenorhabditis elegans. Mammalian Sir2 (SIRT1) has also been found to regulate premature cellular senescence induced by the tumor suppressors PML and p53. SIRT1 plays an important role in cell survival promoted by calorie restriction. Here we show that SIRT1 interacts with WRN both in vitro and in vivo; this interaction is enhanced after DNA damage. WRN can be acetylated by acetyltransferase CBP/p300, and SIRT1 can deacetylate WRN both in vitro and in vivo. WRN acetylation decreases its helicase and exonuclease activities, and SIRT1 can reverse this effect. WRN acetylation alters its nuclear distribution. Down-regulation of SIRT1 reduces WRN translocation from nucleoplasm to nucleoli after DNA damage. These results suggest that SIRT1 regulates WRN-mediated cellular responses to DNA damage through deacetylation of WRN.
DOI of Published Version
J Biol Chem. 2008 Mar 21;283(12):7590-8. Epub 2008 Jan 17. Link to article on publisher's site
The Journal of biological chemistry
Li K, Casta A, Wang R, Lozada EM, Fan W, Kane SE, Ge Q, Gu W, Orren DK, Luo J. (2008). Regulation of WRN protein cellular localization and enzymatic activities by SIRT1-mediated deacetylation. GSBS Student Publications. https://doi.org/10.1074/jbc.M709707200. Retrieved from https://escholarship.umassmed.edu/gsbs_sp/1343