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Publication : Mammalian SIRT1 limits replicative life span in response to chronic genotoxic stress.

First Author  Chua KF Year  2005
Journal  Cell Metab Volume  2
Issue  1 Pages  67-76
PubMed ID  16054100 Mgi Jnum  J:129787
Mgi Id  MGI:3770181 Doi  10.1016/j.cmet.2005.06.007
Citation  Chua KF, et al. (2005) Mammalian SIRT1 limits replicative life span in response to chronic genotoxic stress. Cell Metab 2(1):67-76
abstractText  The Saccharomyces cerevisiae chromatin silencing factor Sir2 suppresses genomic instability and extends replicative life span. In contrast, we find that mouse embryonic fibroblasts (MEFs) deficient for SIRT1, a mammalian Sir2 homolog, have dramatically increased resistance to replicative senescence. Extended replicative life span of SIRT1-deficient MEFs correlates with enhanced proliferative capacity under conditions of chronic, sublethal oxidative stress. In this context, SIRT1-deficient cells fail to normally upregulate either the p19(ARF) senescence regulator or its downstream target p53. However, upon acute DNA damage or oncogene expression, SIRT1-deficient cells show normal p19(ARF) induction and cell cycle arrest. Together, our findings demonstrate an unexpected SIRT1 function in promoting replicative senescence in response to chronic cellular stress and implicate p19(ARF) as a downstream effector in this pathway.
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