Latvian Biomedical Research and Study Centre, Ratsupites iela 1, Riga, LV-1067, Latvia.
Exp Gerontol. 2011 Jul;46(7):560-8. doi: 10.1016/j.exger.2011.02.016. Epub 2011 Mar 3.
Various studies have demonstrated that mitochondrial DNA (mtDNA) heteroplasmy tends to increase with age and that the observed frequency of heteroplasmy among populations mostly depends on the way it is measured. Therefore, we investigated age-related association on the presence of mtDNA heteroplasmy within the hypervariable segment 1 (HVS-I) in a selected study group. The study group consisted of 300 maternally unrelated Latvians ranging in age from 18 to over 90 years. To determine the optimal method for mtDNA heteroplasmy detection, three approaches were used: (i) SURVEYOR Mutation Detection Kit, (ii) sequencing and (iii) denaturing gradient-gel electrophoresis (DGGE). Among the studied individuals, 30.3% were found to be heteroplasmic. The distribution of heteroplasmy statistically significantly increased with individuals' age (17%; 95% confidence interval [CI] 0.095-0.244 in the 18-40 year age group vs. 39%; [CI] 0.294-0.487 in the >90 year age group). Heteroplasmy occurred in a total of 21 different positions within HVS-I, and was the most frequent at fast-mutated positions 16189, 16304 and 16311. The results indicate that heteroplasmy in HVS-I is relatively common and occurs in a broad spectrum of sites. The above is supported by evidence to eventual increase of the probability of heteroplasmy with age due to specific mitochondrial haplogroup background.
各种研究表明,线粒体 DNA(mtDNA)异质性往往随年龄增长而增加,而且在不同人群中观察到的异质性频率主要取决于其测量方式。因此,我们在一个选定的研究组中调查了 mtDNA 异质性在高变区 1(HVS-I)内随年龄的相关性。研究组由 300 名无血缘关系的拉脱维亚人组成,年龄从 18 岁到 90 岁以上。为了确定 mtDNA 异质性检测的最佳方法,我们使用了三种方法:(i)SURVEYOR 突变检测试剂盒,(ii)测序和(iii)变性梯度凝胶电泳(DGGE)。在所研究的个体中,有 30.3%被发现是异质性的。异质性的分布与个体年龄呈统计学显著相关(18-40 岁年龄组为 17%[置信区间(CI)为 0.095-0.244],>90 岁年龄组为 39%[CI 为 0.294-0.487])。异质性发生在 HVS-I 内总共 21 个不同的位置,最常见于快速突变位置 16189、16304 和 16311。结果表明,HVS-I 中的异质性相对常见,发生在广泛的位置。由于特定的线粒体单倍群背景,异质性随年龄增加的可能性最终增加,这一结果提供了证据支持。