Linking DNA Damage, NAD+/SIRT1, and Aging

被引:31
作者
Guarente, Leonard [1 ,2 ]
机构
[1] MIT, Glenn Labs Sci Aging, Cambridge, MA 02139 USA
[2] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
关键词
HISTONE DEACETYLASE; LONGEVITY; MICE;
D O I
10.1016/j.cmet.2014.10.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Diseases due to DNA damage repair machinery defects can resemble premature aging. In this issue of Cell Metabolism, Scheibye-Knudsen et al. (2014) demonstrate that increasing NAD + levels may reverse the inactivation of Sirt1 and mitochondrial defects in Cockayne Syndrome B that stem from nuclear NAD + depletion by the DNA repair protein PARP.
引用
收藏
页码:706 / 707
页数:2
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