Law R H, Farrell L B, Nero D, Devenish R J, Nagley P
Department of Biochemistry, Monash University, Clayton, Victoria, Australia.
FEBS Lett. 1988 Aug 29;236(2):501-5. doi: 10.1016/0014-5793(88)80086-3.
Direct fusions have been constructed between each of subunits 8 and 9 from mitochondrial ATPase of Saccharomyces cerevisiae, proteins normally encoded inside mitochondria, and the cleavable N-terminal transit peptide from the nuclearly encoded precursor to subunit 9 of Neurospora crassa mitochondrial ATPase. The subunit 8 construct was imported efficiently into isolated yeast mitochondria and was processed at or very near the fusion point. When expressed in vivo from its artificial nuclear gene, this cytoplasmically synthesized form of subunit 8 restored the growth defects of aap 1 mutants unable to produce subunit 8 inside the mitochondria. The subunit 9 construct was, however, unable to be imported into isolated mitochondria and could not, following nuclear expression in vivo, complement growth defects in mitochondrial oli 1 mutants. This behaviour is contrasted with the previously demonstrated import competence of another yeast subunit 9 fusion, bearing the first five residues of mature N. crassa subunit 9 interposed between its own transit peptide and the yeast subunit 9 moiety.
酿酒酵母线粒体ATP酶的亚基8和亚基9(通常在线粒体内编码的蛋白质)与粗糙脉孢菌线粒体ATP酶亚基9的核编码前体的可裂解N端转运肽之间构建了直接融合体。亚基8构建体被有效地导入分离的酵母线粒体中,并在融合点处或非常接近融合点处进行加工。当从其人工核基因在体内表达时,这种在细胞质中合成的亚基8形式恢复了无法在线粒体内产生亚基8的aap 1突变体的生长缺陷。然而,亚基9构建体无法导入分离的线粒体,并且在体内进行核表达后,无法弥补线粒体oli 1突变体的生长缺陷。这种行为与先前证明的另一种酵母亚基9融合体的导入能力形成对比,该融合体在其自身的转运肽和酵母亚基9部分之间插入了成熟粗糙脉孢菌亚基9的前五个残基。