Calorie restriction extends yeast life span by lowering the level of NADH

被引:511
作者
Lin, SJ [1 ]
Ford, E
Haigis, M
Liszt, G
Guarente, L
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] Univ Calif Davis, Ctr Genet & Dev, Davis, CA 95616 USA
[3] Univ Calif Davis, Microbiol Sect, Davis, CA 95616 USA
关键词
calorie restriction; longevity regulation; metabolic signaling;
D O I
10.1101/gad.1164804
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Calorie restriction (CR) extends life span in a wide variety of species. Previously, we showed that calorie restriction increases the replicative life span in yeast by activating Sir2, a highly conserved NAD-dependent deacetylase. Here we test whether CR activates Sir2 by increasing the NAD/NADH ratio or by regulating the level of nicotinamide, a known inhibitor of Sir2. We show that CR decreases NADH levels, and that NADH is a competitive inhibitor of Sir2. A genetic intervention that specifically decreases NADH levels increases life span, validating the model that NADH regulates yeast longevity in response to CR.
引用
收藏
页码:12 / 16
页数:5
相关论文
共 34 条
[1]   Nicotinamide and PNC1 govern lifespan extension by calorie restriction in Saccharomyces cerevisiae [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Sinclair, DA .
NATURE, 2003, 423 (6936) :181-185
[2]   Manipulation of a nuclear NAD+ salvage pathway delays aging without altering steady-state NAD+ levels [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Cohen, H ;
Lin, SS ;
Manchester, JK ;
Gordon, JI ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) :18881-18890
[3]   Mutations in Saccharomyces cerevisiae gene SIR2 can have differential effects on in vivo silencing phenotypes and in vitro histone deacetylation activity [J].
Armstrong, CM ;
Kaeberlein, M ;
Imai, SI ;
Guarente, L .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (04) :1427-1438
[4]  
Ashrafi K, 2000, GENE DEV, V14, P1872
[5]   Stoichiometry and compartmentation of NADH metabolism in Saccharomyces cerevisiae [J].
Bakker, BM ;
Overkamp, KM ;
van Maris, AJA ;
Kötter, P ;
Luttik, MAH ;
van Dijken, JP ;
Pronk, JT .
FEMS MICROBIOLOGY REVIEWS, 2001, 25 (01) :15-37
[6]   Inhibition of silencing and accelerated aging by nicotinamide, a putative negative regulator of yeast Sir2 and human SIRT1 [J].
Bitterman, KJ ;
Anderson, RM ;
Cohen, HY ;
Latorre-Esteves, M ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (47) :45099-45107
[7]   Redirection of the respiro-fermentative flux distribution in Saccharomyces cerevisiae by overexpression of the transcription factor Hap4p [J].
Blom, J ;
De Mattos, MJT ;
Grivell, LA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (05) :1970-1973
[8]   A METHOD FOR THE DETERMINATION OF CHANGES OF GLYCOLYTIC METABOLITES IN YEAST ON A SUBSECOND TIME SCALE USING EXTRACTION AT NEUTRAL PH [J].
DEKONING, W ;
VANDAM, K .
ANALYTICAL BIOCHEMISTRY, 1992, 204 (01) :118-123
[9]   GLOBAL REGULATION OF MITOCHONDRIAL BIOGENESIS IN SACCHAROMYCES-CEREVISIAE [J].
DEWINDE, JH ;
GRIVELL, LA .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 46, 1993, 46 :51-91
[10]   Characterization of a trimeric complex containing Oct-1, SNAP(c), and DNA [J].
Ford, E ;
Hernandez, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (25) :16048-16055