Hanna M G, Nelson I P, Morgan-Hughes J A, Harding A E
University Department of Clinical Neurology, Institute of Neurology, London, UK.
J Neurol Sci. 1995 Jun;130(2):154-60. doi: 10.1016/0022-510x(95)00022-t.
The mitochondrial DNA transfer RNA lysine A8344G mutation is commonly associated with the MERRF (myoclonus epilepsy with ragged red fibre) phenotype. The molecular pathogenesis of disease associated with this mutation is unclear. Theoretically, a mitochondrial tRNA mutation might affect transcription or translation, or both. We therefore studied these processes in cloned primary human myoblast cultures containing different proportions of mutant mtDNA. No abnormality of transcription was observed. However, there was a progressive decrease in mitochondrially encoded protein synthesis as the proportion of mutant mtDNA increased. Furthermore, there was evidence that subunits were differentially affected, based on selective reduction of cytochrome c oxidase subunits with relatively low proportions of mutant mtDNA.
线粒体DNA赖氨酸转运RNA A8344G突变通常与肌阵挛性癫痫伴蓬毛样红纤维(MERRF)表型相关。与该突变相关疾病的分子发病机制尚不清楚。从理论上讲,线粒体tRNA突变可能会影响转录或翻译,或者两者都会受到影响。因此,我们在含有不同比例突变型线粒体DNA的克隆原代人成肌细胞培养物中研究了这些过程。未观察到转录异常。然而,随着突变型线粒体DNA比例的增加,线粒体编码的蛋白质合成逐渐减少。此外,有证据表明,基于突变型线粒体DNA比例相对较低时细胞色素c氧化酶亚基的选择性减少,亚基受到的影响存在差异。