Finnegan P M, Ellis T P, Nagley P, Lukins H B
Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia.
FEBS Lett. 1995 Jul 24;368(3):505-8. doi: 10.1016/0014-5793(95)00727-q.
The nucleotide sequence of the yeast nuclear AEP2 gene, required for the expression of the mitochondrial DNA-encoded subunit 9 of ATP synthase, predicts a primary translation product of 67.5 kDa. The ATP13 gene is allelic to AEP2 but was reported to encode a protein of about 42 kDa in size. We thus investigated genetically and biochemically the size of the AEP2 gene product. Genetic complementation assays using 3' truncated AEP2 genes, here shows that function is abolished by the removal of only 32 amino acids from the C-terminus of the predicted protein product. Cell-free translation of AEP2 produces a 64 kDa polypeptide (consistent with the AEP2 sequence) which is imported into mitochondria and processed to a 58 kDa product by the removal of a presequence of about 50 amino acids.
酵母核AEP2基因的核苷酸序列是ATP合酶线粒体DNA编码的亚基9表达所必需的,预测其初级翻译产物为67.5 kDa。ATP13基因与AEP2等位,但据报道编码大小约为42 kDa的蛋白质。因此,我们从遗传和生化方面研究了AEP2基因产物的大小。使用3'截短的AEP2基因进行的遗传互补试验表明,仅从预测的蛋白质产物的C末端去除32个氨基酸就会导致功能丧失。AEP2的无细胞翻译产生一种64 kDa的多肽(与AEP2序列一致),该多肽被导入线粒体,并通过去除约50个氨基酸的前序列加工成58 kDa的产物。