Govindaraju Diddahally, Atzmon Gil, Barzilai Nir
Division of Gerontology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, United States; Institute for Aging Research, Department of Medicine, Albert Einstein College of Medicine, The Bronx, New York, NY 10461, United States.
Institute for Aging Research, Department of Medicine, Albert Einstein College of Medicine, The Bronx, New York, NY 10461, United States; Department of Human Biology, Faculty of Natural Sciences, University of Haifa, Haifa 3498838, Israel.
Appl Transl Genom. 2015 Feb 4;4:23-32. doi: 10.1016/j.atg.2015.01.001. eCollection 2015 Mar.
Longevity as a complex life-history trait shares an ontogenetic relationship with other quantitative traits and varies among individuals, families and populations. Heritability estimates of longevity suggest that about a third of the phenotypic variation associated with the trait is attributable to genetic factors, and the rest is influenced by epigenetic and environmental factors. Individuals react differently to the environments that they are a part of, as well as to the environments they construct for their survival and reproduction; the latter phenomenon is known as niche construction. Lifestyle influences longevity at all the stages of development and levels of human diversity. Hence, lifestyle may be viewed as a component of niche construction. Here, we: a) interpret longevity using a combination of genotype-epigenetic-phenotype (GEP) map approach and niche-construction theory, and b) discuss the plausible influence of genetic and epigenetic factors in the distribution and maintenance of longevity among individuals with normal life span on the one hand, and centenarians on the other. Although similar genetic and environmental factors appear to be common to both of these groups, exceptional longevity may be influenced by polymorphisms in specific genes, coupled with superior genomic stability and homeostatic mechanisms, maintained by negative frequency-dependent selection. We suggest that a comparative analysis of longevity between individuals with normal life span and centenarians, along with insights from population ecology and evolutionary biology, would not only advance our knowledge of biological mechanisms underlying human longevity, but also provide deeper insights into extending healthy life span.
长寿作为一种复杂的生活史特征,与其他数量性状存在个体发育关系,且在个体、家庭和群体之间存在差异。对长寿的遗传力估计表明,与该性状相关的表型变异约有三分之一可归因于遗传因素,其余则受表观遗传和环境因素影响。个体对其所处的环境以及为生存和繁殖所构建的环境反应各异;后一种现象被称为生态位构建。生活方式在人类发展的各个阶段以及多样性层面都会影响长寿。因此,生活方式可被视为生态位构建的一个组成部分。在此,我们:a)运用基因型 - 表观遗传 - 表型(GEP)图谱方法与生态位构建理论相结合来阐释长寿,b)一方面讨论遗传和表观遗传因素对正常寿命个体间长寿分布和维持的可能影响,另一方面讨论对百岁老人的影响。尽管这两组人群似乎都有相似的遗传和环境因素,但超长寿命可能受到特定基因多态性的影响,同时还伴随着由负频率依赖选择维持的卓越基因组稳定性和稳态机制。我们认为,对正常寿命个体与百岁老人之间的长寿进行比较分析,再结合种群生态学和进化生物学的见解,不仅会推进我们对人类长寿背后生物学机制的认识,还能为延长健康寿命提供更深入见解。