Duarte M, Sousa R, Videira A
Instituto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, Portugal.
Genetics. 1995 Mar;139(3):1211-21. doi: 10.1093/genetics/139.3.1211.
We have isolated and characterized the nuclear genes encoding the 12.3-kD subunit of the membrane arm and the 29.9-kD subunit of the peripheral arm of complex I from Neurospora crassa. The former gene was known to be located in linkage group I and the latter is now assigned to linkage group IV of the fungal genome. The genes were separately transformed into different N. crassa strains and transformants with duplicated DNA sequences were isolated. Selected transformants were then mated with other strains to generate repeat-induced point mutations in both copies of the genes present in the nucleus of the parental transformant. From the progeny of the crosses, we were then able to recover two individual mutants lacking the 12.3- and 29.9-kD proteins in their mitochondria, mutants nuo12.3 and nuo29.9, respectively. Several other subunits of complex I are present in the mutant organelles, although with altered stoichiometries as compared with those in the wild-type strain. Based on the analysis of Triton-solubilized mitochondrial complexes in sucrose gradients, neither mutant is able to fully assemble complex I. Our results indicate that mutant nuo12.3 separately assembles the peripheral arm and most of the membrane arm of the enzyme. Mutant nuo29.9 seems to accumulate the membrane arm of complex I and being devoid of the peripheral part. This implicates the 29.9-kD protein in an early step of complex I assembly.
我们已经从粗糙脉孢菌中分离并鉴定了编码膜臂12.3-kD亚基和复合物I外周臂29.9-kD亚基的核基因。已知前一个基因位于连锁群I中,而后一个基因现在被定位到真菌基因组的连锁群IV中。将这些基因分别转化到不同的粗糙脉孢菌菌株中,并分离出具有重复DNA序列的转化体。然后将选定的转化体与其他菌株杂交,以在亲本转化体细胞核中存在的基因的两个拷贝中产生重复诱导的点突变。从杂交后代中,我们随后能够获得两个线粒体中缺乏12.3-kD和29.9-kD蛋白的个体突变体,分别为突变体nuo12.3和nuo29.9。突变细胞器中还存在复合物I的其他几个亚基,尽管与野生型菌株相比其化学计量有所改变。基于对蔗糖梯度中Triton溶解的线粒体复合物的分析,这两个突变体都不能完全组装复合物I。我们的结果表明,突变体nuo12.3分别组装该酶的外周臂和大部分膜臂。突变体nuo29.9似乎积累了复合物I的膜臂,而没有外周部分。这表明29.9-kD蛋白在复合物I组装的早期步骤中起作用。