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The Genetics of Human Longevity

机译:人类长寿的遗传学

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Aging is due to a complex interaction of genetic, epigenetic, and environmental factors, but a strong genetic component appears to have an impact on survival to extreme ages. In order to identify "longevity genes" in humans, different strategies are now available. In our laboratory, we performed association studies on a variety of "candidate" polymorphisms in Italian centenarians. Many genes/polymorphisms gave negative results, while others showed a positive association with human longevity and a sometimes-positive association with unsuccessful aging (myocardial infarction, Alzheimer's disease, and type 2 diabetes). Results regarding genes involved in inflammation (IL-1 cluster, IL-6, IL-10, TNF-α, TGF-β, TLR-4, PPARγ), insulin/IGF-1 signaling pathway and lipid metabolism (apolipoproteins, CETP, PON1), and oxidative stress (p53, p66~(shc)) will be described. In addition, a strong role of the interaction between nuclear and mitochondrial genomes (mtDNA haplogroups and the C150T mutation) emerged from our findings. Thus, the genetics of human longevity appears to be quite peculiar in a context where antagonistic pleiotropy can play a major role and genes can have a different biological role at different ages.
机译:衰老是由于遗传,表观遗传和环境因素之间复杂的相互作用所致,但强大的遗传成分似乎会影响到极端年龄的生存。为了鉴定人类中的“长寿基因”,现在可以使用不同的策略。在我们的实验室中,我们对意大利百岁老人的各种“候选”多态性进行了关联研究。许多基因/多态性给出了阴性结果,而其他一些基因/多态性则与人类寿命呈正相关,而与衰老不成功(心肌梗塞,阿尔茨海默氏病和2型糖尿病)之间的阳性关系有时为正。关于炎症相关基因(IL-1簇,IL-6,IL-10,TNF-α,TGF-β,TLR-4,PPARγ),胰岛素/ IGF-1信号通路和脂质代谢(载脂蛋白,CETP,将描述PON1)和氧化应激(p53,p66〜(shc))。此外,我们的发现还显示出核和线粒体基因组(mtDNA单倍群和C150T突变)之间相互作用的强大作用。因此,在拮抗多效性可能起主要作用而基因在不同年龄可能具有不同的生物学作用的情况下,人类长寿的遗传学似乎是很特殊的。

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