Corral-Debrinski M, Horton T, Lott M T, Shoffner J M, Beal M F, Wallace D C
Department of Genetics and Molecular Medicine, Emory University School of Medicine, Atlanta, Georgia 30322.
Nat Genet. 1992 Dec;2(4):324-9. doi: 10.1038/ng1292-324.
We have examined the role of somatic mitochondrial DNA (mtDNA) mutations in human ageing by quantitating the accumulation of the common 4977 nucleotide pair (np) deletion (mtDNA4977) in the cortex, putamen and cerebellum. A significant increase in the mtDNA4977 deletion was seen in elderly individuals. In the cortex, the deleted to total mtDNA ratio ranged from 0.00023 to 0.012 in 67-77 year old brains and up to 0.034 in subjects over 80. In the putamen, the deletion level ranged from 0.0016 to 0.010 in 67 to 77 years old up to 0.12 in individuals over the age of 80. The cerebellum remained relatively devoid of mtDNA deletions. Similar changes were observed with a different 7436 np deletion. These changes suggest that somatic mtDNA deletions might contribute to the neurological impairment often associated with ageing.
我们通过定量分析大脑皮层、壳核和小脑中常见的4977个核苷酸对(np)缺失(mtDNA4977)的积累情况,研究了体细胞线粒体DNA(mtDNA)突变在人类衰老过程中的作用。在老年人中观察到mtDNA4977缺失显著增加。在大脑皮层中,67至77岁人群的大脑中缺失的mtDNA与总mtDNA的比例范围为0.00023至0.012,而80岁以上人群中该比例高达0.034。在壳核中,67至77岁人群的缺失水平范围为0.0016至0.010,80岁以上个体中则高达0.12。小脑相对较少存在mtDNA缺失。对于另一种7436 np缺失,也观察到了类似的变化。这些变化表明,体细胞mtDNA缺失可能导致了常与衰老相关的神经功能损害。