Atzmon Gil, Cho Miook, Cawthon Richard M, Budagov Temuri, Katz Micol, Yang Xiaoman, Siegel Glenn, Bergman Aviv, Huffman Derek M, Schechter Clyde B, Wright Woodring E, Shay Jerry W, Barzilai Nir, Govindaraju Diddahally R, Suh Yousin
Department of Medicine and Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Proc Natl Acad Sci U S A. 2010 Jan 26;107 Suppl 1(Suppl 1):1710-7. doi: 10.1073/pnas.0906191106. Epub 2009 Nov 13.
Telomere length in humans is emerging as a biomarker of aging because its shortening is associated with aging-related diseases and early mortality. However, genetic mechanisms responsible for these associations are not known. Here, in a cohort of Ashkenazi Jewish centenarians, their offspring, and offspring-matched controls, we studied the inheritance and maintenance of telomere length and variations in two major genes associated with telomerase enzyme activity, hTERT and hTERC. We demonstrated that centenarians and their offspring maintain longer telomeres compared with controls with advancing age and that longer telomeres are associated with protection from age-related diseases, better cognitive function, and lipid profiles of healthy aging. Sequence analysis of hTERT and hTERC showed overrepresentation of synonymous and intronic mutations among centenarians relative to controls. Moreover, we identified a common hTERT haplotype that is associated with both exceptional longevity and longer telomere length. Thus, variations in human telomerase gene that are associated with better maintenance of telomere length may confer healthy aging and exceptional longevity in humans.
人类的端粒长度正逐渐成为衰老的生物标志物,因为其缩短与衰老相关疾病和早逝有关。然而,导致这些关联的遗传机制尚不清楚。在此,在一组阿什肯纳兹犹太百岁老人、他们的后代以及与后代匹配的对照组中,我们研究了端粒长度的遗传和维持情况,以及与端粒酶活性相关的两个主要基因hTERT和hTERC的变异。我们证明,与年龄增长的对照组相比,百岁老人及其后代维持着更长的端粒,并且更长的端粒与预防年龄相关疾病、更好的认知功能以及健康衰老的脂质谱相关。hTERT和hTERC的序列分析表明,相对于对照组,百岁老人中同义突变和内含子突变的比例过高。此外,我们鉴定出一种常见的hTERT单倍型,它与超长寿命和更长的端粒长度都有关联。因此,与端粒长度更好维持相关的人类端粒酶基因变异可能赋予人类健康衰老和超长寿命。