Kujoth Gregory C, Leeuwenburgh Christiaan, Prolla Tomas A
Department of Genetics and Medical Genetics, University of Wisconsin, 425-G Henry Mall, Madison, WI 53706, USA.
Cancer Res. 2006 Aug 1;66(15):7386-9. doi: 10.1158/0008-5472.CAN-05-4670.
Mutations in mitochondrial DNA (mtDNA) accumulate during aging, but their significance to longevity and age-associated disease has been uncertain. Recently, in support of the hypothesis that mtDNA integrity is important, we have shown that age-associated diseases arise more rapidly in mice where mtDNA mutations and increased levels of apoptosis occur at higher rates than normal due to expression of an error-prone mtDNA polymerase. Further studies in this model may provide deeper insights into the relationship between mitochondria, aging, and susceptibility to age-associated diseases, such as cancer.
线粒体DNA(mtDNA)突变在衰老过程中会不断积累,但其对寿命和与年龄相关疾病的影响尚不确定。最近,为支持mtDNA完整性很重要这一假说,我们发现,由于一种易出错的mtDNA聚合酶的表达,mtDNA突变和凋亡水平升高的小鼠比正常小鼠更快出现与年龄相关的疾病。对该模型的进一步研究可能会更深入地揭示线粒体、衰老以及对癌症等与年龄相关疾病易感性之间的关系。