Lemaire C, Robineau S, Netter P
Centre de Génétique Moléculaire, Laboratoire propre du CNRS associé à l'Université Pierre et Marie Curie, F-91198 Gif-sur-Yvette cedex, France.
Curr Genet. 1998 Aug;34(2):138-45. doi: 10.1007/s002940050378.
We report on the molecular and biochemical analysis of a set of 13 respiratory deficient mutants of Saccharomyces cerevisiae which are specifically altered in COX1, the gene encoding the subunit Cox1p of cytochrome c oxidase. DNA sequence analysis shows that three are due to frameshift mutations, two to nonsense mutations, and eight to missense mutations. All, except the missense mutant S157L, have impaired electron transfer and respiratory activity. Analysis of the mitochondrial translation products shows that when Cox1p is absent, Cox2p and Cox3p are still synthesized. In the missense mutants, the steady state levels in the mitochondrial membranes of the three mitochondrially encoded subunits Cox1p, Cox2p and Cox3p and the nuclear-encoded subunit Cox4p are reduced. In the frameshift and nonsense mutants, Cox1p is absent and Cox2p, Cox3p and Cox4p are considerably decreased or undetectable. A comparison of the steady state levels of Cox1p through Cox4p in the COX1, COX2, COX3 and COX4 mutants shows the interdependance of the accumulation of these four subunits in the mitochondrial membranes.
我们报告了一组13个酿酒酵母呼吸缺陷型突变体的分子和生化分析,这些突变体在细胞色素c氧化酶亚基Cox1p的编码基因COX1中发生了特异性改变。DNA序列分析表明,其中三个是由于移码突变,两个是由于无义突变,八个是由于错义突变。除了错义突变体S157L外,所有突变体的电子传递和呼吸活性均受损。线粒体翻译产物分析表明,当Cox1p缺失时,Cox2p和Cox3p仍能合成。在错义突变体中,线粒体编码的三个亚基Cox1p、Cox2p和Cox3p以及核编码亚基Cox4p在线粒体膜中的稳态水平降低。在移码突变体和无义突变体中,Cox1p缺失,Cox2p、Cox3p和Cox4p显著减少或无法检测到。对COX1、COX2、COX3和COX4突变体中Cox1p至Cox4p的稳态水平进行比较,显示了这四个亚基在线粒体膜中积累的相互依赖性。