Linking chromatin function with metabolic networks:: Sir2 family of NAD+-dependent deacetylases

被引:179
作者
Denu, JM [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA
关键词
D O I
10.1016/S0968-0004(02)00005-1
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
Chromatin remodeling enzymes rely on coenzymes derived from metabolic pathways, suggesting a tight synchronization among apparently diverse cellular processes. A unique example of this link is the recently described NAD(+)-dependent protein and/or histone deacetylases. The founding member of this family - yeast silent information regulator 2 (ySir2) - is involved in gene silencing, chromosomal stability and ageing. Sir2-like enzymes catalyze a reaction in which the cleavage of NAD(+)and histone and/or protein deacetylation are coupled to the formation of O-acetyl-ADP-ribose, a novel metabolite. The dependence of the reaction on both NAD(+) and the generation of this potential second messenger offers new clues to understanding the function and regulation of nuclear, cytoplasmic and mitochondrial Sir2-like enzymes.
引用
收藏
页码:41 / 48
页数:8
相关论文
共 70 条
[61]   Net1, a Sir2-associated nucleolar protein required for rDNA silencing and nucleolar integrity [J].
Straight, AF ;
Shou, WY ;
Dowd, GJ ;
Turck, CW ;
Deshaies, RJ ;
Johnson, AD ;
Moazed, D .
CELL, 1999, 97 (02) :245-256
[62]   Silent information regulator 2 family of NAD-dependent histone/protein deacetylases generates a unique product, 1-O-acetyl-ADP-ribose [J].
Tanner, KG ;
Landry, J ;
Sternglanz, R ;
Denu, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14178-14182
[63]   Coupling of histone deacetylation to NAD breakdown by the yeast silencing protein Sir2: Evidence for acetyl transfer from substrate to an NAD breakdown product [J].
Tanny, JC ;
Moazed, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :415-420
[64]   An enzymatic activity in the yeast Sir2 protein that is essential for gene silencing [J].
Tanny, JC ;
Dowd, GJ ;
Huang, J ;
Hilz, H ;
Moazed, D .
CELL, 1999, 99 (07) :735-745
[65]   Increased dosage of a sir-2 gene extends lifespan in Caenorhabditis elegans [J].
Tissenbaum, HA ;
Guarente, L .
NATURE, 2001, 410 (6825) :227-230
[66]   CobB, a new member of the SIR2 family of eucaryotic regulatory proteins, is required to compensate for the lack of nicotinate mononucleotide:5,6-dimethylbenzimidazole phosphoribosyltransferase activity in cobT mutants during cobalamin biosynthesis in Salmonella typhimurium LT2 [J].
Tsang, AW ;
Escalante-Semerena, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :31788-31794
[67]   hSIR2SIRT1 functions as an NAD-dependent p53 deacetylase [J].
Vaziri, H ;
Dessain, SK ;
Eagon, EN ;
Imai, SI ;
Frye, RA ;
Pandita, TK ;
Guarente, L ;
Weinberg, RA .
CELL, 2001, 107 (02) :149-159
[68]   Global histone acetylation and deacetylation in yeast [J].
Vogelauer, M ;
Wu, JS ;
Suka, N ;
Grunstein, M .
NATURE, 2000, 408 (6811) :495-498
[69]  
Zhang QH, 2002, SCIENCE, V295, P1895
[70]   New functions of a long-known molecule - Emerging roles of NAD in cellular signaling [J].
Ziegler, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (06) :1550-1564