Bonnefoy N, Kermorgant M, Groudinsky O, Minet M, Slonimski P P, Dujardin G
Centre de Génétique Moléculaire du Centre National de la Recherche Scientifique, Laboratoire propre associé à l'université Pierre et Marie Curie, Gif-sur-Yvette, France.
Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):11978-82. doi: 10.1073/pnas.91.25.11978.
The yeast nuclear gene OXA1 is essential for cytochrome oxidase assembly, so that a null mutation in the OXA1 gene leads to complete respiratory deficiency. We have cloned by genetic selection a human OXA1 (OXA1Hs) cDNA that complements the respiratory defect of yeast oxa1 mutants. The deduced sequence of the human protein shares 33% identity with the yeast OXA1 protein. The OXA1Hs cDNA corresponds to a single and relatively highly expressed gene. Oxygen consumption measurements and cytochrome absorption spectra show that replacement of the yeast protein with the human homolog leads to the correct assembly of cytochrome oxidase, suggesting that the proteins play essentially the same role in both organisms.
酵母核基因OXA1对细胞色素氧化酶的组装至关重要,因此OXA1基因的无效突变会导致完全呼吸缺陷。我们通过遗传筛选克隆了一个人类OXA1(OXA1Hs)cDNA,它能弥补酵母oxa1突变体的呼吸缺陷。推导的人类蛋白质序列与酵母OXA1蛋白质有33%的同一性。OXA1Hs cDNA对应于一个单一且表达相对较高的基因。氧气消耗测量和细胞色素吸收光谱表明,用人源同源物替代酵母蛋白可导致细胞色素氧化酶的正确组装,这表明这两种蛋白质在两种生物体中发挥着基本相同的作用。