The biochemistry of sirtuins

被引:613
作者
Sauve, Anthony A. [1 ]
Wolberger, Cynthia
Schramm, Vern L.
Boeke, Jef D.
机构
[1] Cornell Univ, Weill Med Coll, Dept Pharmacol, New York, NY 10021 USA
[2] Johns Hopkins Univ, Howard Hughes Med Inst, Dept Biophys & Biophys Chem, Baltimore, MD 21205 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10465 USA
[4] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
关键词
Sir2; deacetylase; longevity; O-acetyl-ADP-ribose; NAD(+); gene silencing;
D O I
10.1146/annurev.biochem.74.082803.133500
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sirtuins are a family of NAD(+)-dependent protein deacetylascs widely distributed in all phyla of life. Accumulating evidence indicates that sirtuins are important regulators of organism life span. In yeast, these unique enzymes regulate gene silencing by histone deacetylation and via formation of the novel compound 2'-O-acetylADP-ribose. In multicellular organisms, sirtuins deacetylate histones and transcription factors that regulate stress, metabolism, and survival pathways. The chemical mechanism of sirtuins provides novel opportunities for signaling and metabolic regulation of protein deacetylation. The biological, chemical, and structural characteris tics of these unusual enzymes are discussed in this review.
引用
收藏
页码:435 / 465
页数:31
相关论文
共 130 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]  
[Anonymous], ENZYMES
[3]   MODIFIERS OF POSITION EFFECT ARE SHARED BETWEEN TELOMERIC AND SILENT MATING-TYPE LOCI IN SACCHAROMYCES-CEREVISIAE [J].
APARICIO, OM ;
BILLINGTON, BL ;
GOTTSCHLING, DE .
CELL, 1991, 66 (06) :1279-1287
[4]   Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration [J].
Araki, T ;
Sasaki, Y ;
Milbrandt, J .
SCIENCE, 2004, 305 (5686) :1010-1013
[5]   Mechanism of sirtuin inhibition by nicotinamide:: Altering the NAD+ cosubstrate specificity of a Sir2 enzyme [J].
Avalos, JL ;
Bever, KM ;
Wolberger, C .
MOLECULAR CELL, 2005, 17 (06) :855-868
[6]   Structural basis for the mechanism and regulation of Sir2 enzymes [J].
Avalos, JL ;
Boeke, JD ;
Wolberger, C .
MOLECULAR CELL, 2004, 13 (05) :639-648
[7]   Structure of a Sir2 enzyme bound to an acetylated p53 peptide [J].
Avalos, JL ;
Celic, I ;
Muhammad, S ;
Cosgrove, MS ;
Boeke, JD ;
Wolberger, C .
MOLECULAR CELL, 2002, 10 (03) :523-535
[8]   Identification of a small molecule inhibitor of Sir2p [J].
Bedalov, A ;
Gatbonton, T ;
Irvine, WP ;
Gottschling, DE ;
Simon, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (26) :15113-15118
[9]  
Bell CE, 1997, PROTEIN SCI, V6, P2084
[10]   The interaction of Alba, a conserved archaeal, chromatin protein, with Sir2 and its regulation by acetylation [J].
Bell, SD ;
Botting, CH ;
Wardleworth, BN ;
Jackson, SP ;
White, MF .
SCIENCE, 2002, 296 (5565) :148-151