Masuyama Mika, Iida Reiko, Takatsuka Hisakazu, Yasuda Toshihiro, Matsuki Takasumi
Department of Forensic Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka-cho, Fukui 910-1193, Japan.
Biochim Biophys Acta. 2005 May 25;1723(1-3):302-8. doi: 10.1016/j.bbagen.2005.03.001. Epub 2005 Mar 17.
In order to systematically characterize age-related changes in the mtDNA content of various tissues during aging, we analyzed the mtDNA content of eight tissues from mice at five different ages from young to senescent by quantitative real-time PCR analysis. Obvious variations of mtDNA content among the tissues were detected: There was a 20-fold range in 2-week-old mice and a 50-fold range in 15-month-old mice. The mtDNA contents of the heart, lung, kidney, spleen and skeletal muscle increased gradually with age, whereas those of bone marrow and brain showed no age-related pattern. The expression patterns of mitochondrial transcription factor A (mtTFA) and mitochondrial single-strand DNA binding protein (mtSSB), possible regulatory factors of the mtDNA copy number, were not necessarily linked with the age-related pattern of the mtDNA content, suggesting the existence of other factors that affect the mtDNA content. The Western blot analysis of mtDNA-encoded cytochrome c oxidase subunit III (MTCO3) demonstrated that the expression levels of this protein in the heart and skeletal muscle increase with age in parallel with the mtDNA content. These findings confirm that the mtDNA content of tissues changes during aging.
为了系统地表征衰老过程中各组织线粒体DNA(mtDNA)含量的年龄相关变化,我们通过定量实时PCR分析,对从幼年到衰老的五个不同年龄阶段小鼠的八个组织的mtDNA含量进行了分析。检测到各组织间mtDNA含量存在明显差异:2周龄小鼠中差异范围为20倍,15月龄小鼠中差异范围为50倍。心脏、肺、肾、脾和骨骼肌的mtDNA含量随年龄逐渐增加,而骨髓和脑的mtDNA含量则未显示出与年龄相关的模式。线粒体转录因子A(mtTFA)和线粒体单链DNA结合蛋白(mtSSB)作为mtDNA拷贝数可能的调节因子,其表达模式不一定与mtDNA含量的年龄相关模式相关联,这表明存在其他影响mtDNA含量的因素。对mtDNA编码的细胞色素c氧化酶亚基III(MTCO3)的蛋白质免疫印迹分析表明,该蛋白在心脏和骨骼肌中的表达水平随年龄增加,与mtDNA含量平行。这些发现证实了衰老过程中组织的mtDNA含量会发生变化。