Brigham and Women's Hospital, Harvard Medical School, Boston, United States.
Gero LLC, Moscow, Russian Federation.
Elife. 2020 Apr 7;9:e53449. doi: 10.7554/eLife.53449.
Heritability of human lifespan is 23-33% as evident from twin studies. Genome-wide association studies explored this question by linking particular alleles to lifespan traits. However, genetic variants identified so far can explain only a small fraction of lifespan heritability in humans. Here, we report that the burden of rarest protein-truncating variants (PTVs) in two large cohorts is negatively associated with human healthspan and lifespan, accounting for 0.4 and 1.3 years of their variability, respectively. In addition, longer-living individuals possess both fewer rarest PTVs and less damaging PTVs. We further estimated that somatic accumulation of PTVs accounts for only a small fraction of mortality and morbidity acceleration and hence is unlikely to be causal in aging. We conclude that rare damaging mutations, both inherited and accumulated throughout life, contribute to the aging process, and that burden of ultra-rare variants in combination with common alleles better explain apparent heritability of human lifespan.
从双胞胎研究中可以明显看出,人类寿命的遗传性为 23-33%。全基因组关联研究通过将特定的等位基因与寿命特征联系起来,探讨了这个问题。然而,迄今为止发现的遗传变异只能解释人类寿命遗传率的一小部分。在这里,我们报告说,在两个大型队列中,最稀有的蛋白质截断变异(PTV)的负担与人类健康寿命和寿命呈负相关,分别解释了它们可变性的 0.4 和 1.3 年。此外,寿命较长的个体拥有更少的最稀有的 PTV 和更少的破坏性 PTV。我们进一步估计,体细胞积累的 PTV 仅占死亡率和发病率加速的一小部分,因此不太可能是衰老的原因。我们的结论是,罕见的破坏性突变,无论是遗传的还是一生中积累的,都有助于衰老过程,并且超罕见变异的负担与常见等位基因相结合,可以更好地解释人类寿命的明显遗传性。