Pulkes T, Sweeney M G, Hanna M G
Lancet. 2000 Dec 16;356(9247):2068-9. doi: 10.1016/s0140-6736(00)03408-5.
Factors which increase the risk of stroke in patients with the A3243G (mitochondrial encephalomyopathy, lactic acidosis, and stroke [MELAS]) mutation in human mitochondrial DNA are unclear. Previous work on lung-cancer cells with an A3243G mutation showed that a mutation in the mitochondrial transfer gene for leucine tRNA(Leu(CUN)) was able to ameliorate the A3243G-induced biochemical phenotype. We analysed the tRNA(Leu(CUN)) gene in 48 unrelated A3243G cases. We showed that a polymorphism, A12308G, in tRNA(Leu(CUN)) increases the risk of developing stroke in patients with the A3243G mutation (relative risk=2.17). This may have implications for genetic counselling.
人类线粒体DNA中A3243G(线粒体脑肌病、乳酸酸中毒和卒中[MELAS])突变患者发生卒中风险增加的因素尚不清楚。先前对具有A3243G突变的肺癌细胞的研究表明,亮氨酸tRNA(Leu(CUN))的线粒体转移基因突变能够改善A3243G诱导的生化表型。我们分析了48例无亲缘关系的A3243G病例中的tRNA(Leu(CUN))基因。我们发现,tRNA(Leu(CUN))中的一个多态性A12308G增加了A3243G突变患者发生卒中的风险(相对风险=2.17)。这可能对遗传咨询有影响。