A novel VNTR enhancer within the SIRT3 gene, a human homologue of SIR2, is associated with survival at oldest ages

被引:290
作者
Bellizzi, D
Rose, G
Cavalcante, P
Covello, G
Dato, S
De Rango, F
Greco, V
Maggiolini, M
Feraco, E
Mari, V
Franceschi, C
Passarino, G
De Benedictis, G [1 ]
机构
[1] Univ Calabria, Dept Cell Biol, I-87036 Cosenza, Italy
[2] Univ Calabria, Dept Pharmacobiol, I-87036 Cosenza, Italy
[3] Ist Nazl Riposo & Cura Anziano, Cosenza, Italy
[4] Univ Bologna, Dept Expt Pathol, I-40126 Bologna, Italy
关键词
SIRT3; human longevity; VNTR enhancer;
D O I
10.1016/j.ygeno.2004.11.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
SIR2 genes control life span in model organisms, playing a central role in evolutionarily conserved pathways of aging and longevity. We wanted to verify whether similar effects may act in humans too. First, we searched for variability in the human sirtuin 3 gene (SIRT3) and discovered a VNTR polymorphism (72-bp repeat core) in intron 5. The alleles differed both for the number of repeats and for presence/absence of potential regulatory sites. Second, by transient transfection experiments, we demonstrated that the VNTR region has an allele-specific enhancer activity. Third, by analyzing allele frequencies as a function of age in a sample of 945 individuals (20-106 years), we found that the allele completely lacking enhancer activity is virtually absent in males older than 90 years. Thus the underexpression of a human sirtuin gene seems to be detrimental for longevity as it occurs in model organisms. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:258 / 263
页数:6
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