Glerum D M, Tzagoloff A
Department of Biological Sciences, Columbia University, New York, NY 10027.
Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8452-6. doi: 10.1073/pnas.91.18.8452.
We have cloned the human homolog of the Saccharomyces cerevisiae COX10 gene by functional complementation of a yeast cox10 null mutant. The 2.8-kb cDNA encoding the human heme A:farnesyltransferase codes for a 443-aa protein with high homology to the yeast and bacterial farnesylases. The human COX10 homolog, however, does not complement the mutation as efficiently as the yeast COX10 protein, likely due to the heterologous environment. PCR amplification and Southern analysis confirm the existence of a large mRNA for the human protein, with an unusually long 3' untranslated region. This clone can now be used to screen patients with inherited deficiencies in cytochrome oxidase in which the mutations remain unidentified and are likely to reside in a protein influencing the assembly of the enzyme.
我们通过对酵母cox10缺失突变体进行功能互补,克隆了酿酒酵母COX10基因的人类同源物。编码人类血红素A:法尼基转移酶的2.8kb cDNA编码一种443个氨基酸的蛋白质,与酵母和细菌法尼基转移酶具有高度同源性。然而,人类COX10同源物对突变的互补效率不如酵母COX10蛋白,这可能是由于异源环境所致。PCR扩增和Southern分析证实了人类蛋白质存在一个大的mRNA,其3'非翻译区异常长。该克隆现在可用于筛选细胞色素氧化酶遗传性缺陷患者,这些患者的突变尚未确定,且可能存在于影响该酶组装的蛋白质中。