Vázquez-Memije M E, Shanske S, Santorelli F M, Kranz-Eble P, DeVivo D C, DiMauro S
Unidad de Investigación en Genética Humana, Hospital de Pediatría, Centro Médico Nacional-IMSS, México, D.F.
J Inherit Metab Dis. 1998 Dec;21(8):829-36. doi: 10.1023/a:1005418718299.
We performed comparative biochemical studies in cultured fibroblast mitochondria from patients with the T8993G or the T8993C point mutations in the ATPase 6 gene of mitochondrial DNA. We found that ATP production was much more severely decreased in cells from patients with the T8993G mutation than in those from patients with the T8993C mutation. Kinetic studies suggest that both mutations affect only the F0 sector of the mitochondrial ATPase complex. We conclude that these two mutations, which result in the substitution of different amino acids at the same site of the ATPase, result in an enzyme with different biochemical characteristics.
我们对线粒体DNA中ATP酶6基因存在T8993G或T8993C点突变的患者的培养成纤维细胞线粒体进行了比较生化研究。我们发现,T8993G突变患者的细胞中ATP生成的减少程度比T8993C突变患者的细胞严重得多。动力学研究表明,这两种突变仅影响线粒体ATP酶复合体的F0部分。我们得出结论,这两种突变在ATP酶的同一位置导致不同氨基酸的替代,产生了具有不同生化特性的酶。