Zole Egija, Zadinane Krista, Pliss Liana, Ranka Renate
a Latvian Biomedical Research and Study Centre , Riga , Latvia.
b Faculty of Biology , University of Latvia , Riga , Latvia.
Mitochondrial DNA A DNA Mapp Seq Anal. 2018 Apr;29(3):431-438. doi: 10.1080/24701394.2017.1303490. Epub 2017 Mar 24.
We studied telomere length (TL) and mitochondrial DNA (mtDNA) copy number variations in individuals from Latvian Caucasian population in different age groups. We showed a positive correlation between TL and mtDNA copy number in individuals of up to 90 years of age; however, this correlation was not observed in the 90-100 years age group. While TL shortened with age and mtDNA content decreased with increasing age, in this study it was observed that mtDNA copy number in nonagenarians was slightly higher than in the 60-89 years age group. The presence of heteroplasmy in the mtDNA HVS-I control region did not correlate with TL and mtDNA copy number. TL and mtDNA values also did not differ between mitochondrial haplogroups. In conclusion, while both TL and mtDNA are involved in the aging process and link between these cell components exists, nonagenarians may have differences in senescence-related pathways and systems, which may function as a protective mechanism that allows them to live longer.
我们研究了不同年龄组拉脱维亚高加索人群个体的端粒长度(TL)和线粒体DNA(mtDNA)拷贝数变异。我们发现,90岁及以下个体的TL与mtDNA拷贝数呈正相关;然而,在90至100岁年龄组中未观察到这种相关性。虽然TL随年龄增长而缩短,mtDNA含量也随年龄增加而减少,但在本研究中观察到,九旬老人的mtDNA拷贝数略高于60至89岁年龄组。mtDNA高变区I(HVS-I)控制区异质性的存在与TL和mtDNA拷贝数无关。不同线粒体单倍群之间的TL和mtDNA值也没有差异。总之,虽然TL和mtDNA都参与衰老过程且这些细胞成分之间存在联系,但九旬老人在衰老相关途径和系统方面可能存在差异,这可能作为一种保护机制,使他们能够活得更长。