Ege University School of Medicine, Department of Medical Biochemistry, Izmir, Turkey.
Ege University School of Medicine, Department of Medical Biochemistry, Izmir, Turkey.
Mitochondrion. 2014 Jul;17:7-13. doi: 10.1016/j.mito.2014.04.013. Epub 2014 May 2.
The accumulation of mutations in mitochondrial DNA is a widely recognized mechanism for aging and age related diseases. However, studies indicate that some mutations could be beneficial to longevity by slowing down the function of the electron transport chain, reducing free radical production. In this study, we re-sequenced the entire mitochondrial DNA from 50 individuals and examined aging-related variations in the Turkish population. We evaluated sequence data by comparing whole SNP frequencies, individual SNP frequencies, the effect of SNPs, SNP accumulation in certain mtDNA regions and haplotype profiles between elderly and control groups. The frequency of total mitochondrial SNPs was significantly higher in nonagenarians than controls (p=0.0094). Furthermore, non-coding, synonymous and tRNA mutations were more prevalent in the 90+ group compared to controls (p=0.0001, p<0.001, p=0.0096, respectively). A73G and C152T polymorphisms were significantly associated with longevity in the Turkish population (p=0.0086 and p=0.004, respectively). Additionally, C150T was specific to the 90+ group, but the difference failed to reach statistical significance (p=0.053). We also detected a novel transversion in the ATPase6 gene (C8899A) that was negatively associated with longevity (p=0.0016). Examining the distribution of SNPs among genes and functionally associated gene regions revealed a significant accumulation of mutations in the D-loop region and genes encoding Complex I subunits (ND1-6) (p<0.0001, p=0.0302, respectively). Moreover, there was an increase in the non-synonymous mutation frequency of Complex I genes in aged subjects (p<0.0001). Haplotype H was also significantly increased in the control group (p=0.0405). Overall, our findings support a role for mitochondrial genome variations and the functionality of oxidative phosphorylation in longevity. In this report, we sequenced the whole mtDNA of the Turkish population for the first time.
线粒体 DNA 突变的积累是衰老和与年龄相关疾病的广泛认可的机制。然而,研究表明,一些突变可能通过减缓电子传递链的功能、减少自由基的产生而有益于长寿。在这项研究中,我们对 50 个人的整个线粒体 DNA 进行了重新测序,并研究了土耳其人群中的与衰老相关的变异。我们通过比较老年组和对照组的全 SNP 频率、个体 SNP 频率、SNP 的影响、某些 mtDNA 区域 SNP 的积累以及单倍型谱,对序列数据进行了评估。非百岁老人的总线粒体 SNP 频率明显高于对照组(p=0.0094)。此外,与对照组相比,90 岁以上组中非编码区、同义突变和 tRNA 突变更为常见(p=0.0001、p<0.001、p=0.0096)。A73G 和 C152T 多态性与土耳其人群的长寿显著相关(p=0.0086 和 p=0.004)。此外,C150T 仅存在于 90 岁以上组,但差异无统计学意义(p=0.053)。我们还在 ATPase6 基因中检测到一个新的颠换(C8899A),该突变与长寿呈负相关(p=0.0016)。检查基因和功能相关基因区域的 SNP 分布显示,D 环区和编码复合物 I 亚基(ND1-6)的基因突变显著积累(p<0.0001、p=0.0302)。此外,老年组中非同义突变频率的复合物 I 基因也增加(p<0.0001)。控制组中的单倍型 H 也显著增加(p=0.0405)。总的来说,我们的研究结果支持线粒体基因组变异和氧化磷酸化功能在长寿中的作用。在本报告中,我们首次对土耳其人群的整个 mtDNA 进行了测序。