Variability of the SIRT3 gene, human silent information regulator Sir2 homologue, and survivorship in the elderly

被引:293
作者
Rose, G
Dato, S
Altomare, K
Bellizzi, D
Garasto, S
Greco, V
Passarino, G
Feraco, E
Mari, V
Barbi, C
BonaFe, M
Franceschi, C
Tan, Q
Boiko, S
Yashin, AI
De Benedictis, G [1 ]
机构
[1] Univ Calabria, Dept Cell Biol, I-87030 Arcavacata Di Rende, Italy
[2] INRCA, Italian Natl Res Ctr Aging, Cosenza, Italy
[3] Univ Bologna, Dept Mol Pathol, Bologna, Italy
[4] Univ So Denmark, Dept Clin Biochem, Odense, Denmark
[5] Max Planck Inst Demograph Res, Rostock, Germany
关键词
SIRT3; gene; human longevity; Silent Information Regulator 2 homologue;
D O I
10.1016/S0531-5565(03)00209-2
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
The human sirtuin 3 (SIRT3) gene encodes a putative mitochondrial NAD-dependent deacetylase (SIRT3) which belongs to the evolutionary conserved family of sirtuin 2 proteins. Studies in model organisms have demonstrated that SIR2 genes control lifespan, while no data are available regarding a possible role of SIRT3 in human longevity. By analysing the genotype-specific survival function relevant to the G477T marker of SIRT3, we found that in males the TT genotype increases (p = 0.0272), while the GT genotype decreases (p = 0.0391) survival in the elderly. Since SIRT3 lies in a chromosomal region (11p15.5) where four genes potentially associated with longevity are located (HRAS1, Insulin-like Growth Factor 2, Proinsulin, and Tyrosine Hydroxylase) we tested for linkage-disequilibrium between G477T alleles and alleles of the above genes. The disequilibrium was not significant in any case, thus suggesting that SIRT3 itself, or a gene strictly linked to SIRT3, may have a role in human longevity. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1065 / 1070
页数:6
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