The variability of the mitochondrial genome in human aging: a key for life and death?

被引:32
作者
Rose, G
Passarino, G
Franceschi, C
De Benedictis, G [1 ]
机构
[1] Univ Calabria, Dept Cell Biol, I-87030 Commenda Di Rende, Italy
[2] Univ Bologna, Dept Expt Pathol, I-40126 Bologna, Italy
关键词
mtDNA; programmed death; human aging; longevity;
D O I
10.1016/S1357-2725(02)00042-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The impressive performance of the research in mitochondrial genetics and human aging in the last decade outlines a new scenery in which the inherited variation of the mitochondrial genome (mtDNA) may play a role in rate and quality of aging. This variation in humans was initially looked at as nearly neutral, and useful just for the reconstruction of human population history. However, recent data suggest that different mtDNA molecules are qualitatively different from each other. The aim of this paper is to discuss current ideas on the relationships among mitochondrial function, mtDNA inherited variation, and aging. The main processes where the mitochondrion is involved and the importance these processes have on aging and death of individuals will be described. A possible connection between programmed death phenomena (mitoptosis, apoptosis, phenoptosis) and rate and quality of aging will be discussed. Finally, the possible role played in these processes by the mtDNA germline variation will be explored. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1449 / 1460
页数:12
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