Jin C, Myers A M, Tzagoloff A
Department of Biological Sciences, Columbia University, New York, NY 10027, USA.
Curr Genet. 1997 Mar;31(3):228-34. doi: 10.1007/s002940050199.
The nuclear gene MRP10 of Saccharomyces cerevisiae was cloned by complementation of a respiratory deficient mutant N518/L1. This mutant is defective in mitochondrial translation and shows a tendency to accumulate deletions in mitochondrial DNA (rho-). Analysis revealed Mrp10p to be a component of the 37 S subunit of the mitochondrial ribosomes. Disruption of MRP10 in a haploid strain of yeast elicits a phenotype identical to that of the original mutant. The respiratory defect of the null mutant is rescued by re-introducing the MRP10 gene in a wild-type mitochondrial DNA background. These results indicate that Mrp10p belongs to the class of yeast mitochondrial ribosomal proteins that are essential for translation. Searches of current databases failed to reveal any homologs among known bacterial or eucaryotic cytoplasmic ribosomal proteins. Some sequence similarity, however, was detected between Mrp10p and Yml37p, previously identified as a component of the yeast mitochondrial 50 S ribosomal subunit.
通过对呼吸缺陷型突变体N518/L1进行互补,克隆了酿酒酵母的核基因MRP10。该突变体在线粒体翻译方面存在缺陷,并且显示出线粒体DNA(rho-)中缺失积累的趋势。分析表明Mrp10p是线粒体核糖体37 S亚基的一个组成部分。在酵母单倍体菌株中破坏MRP10会引发与原始突变体相同的表型。通过在野生型线粒体DNA背景中重新引入MRP10基因,可挽救无效突变体的呼吸缺陷。这些结果表明,Mrp10p属于对翻译至关重要的酵母线粒体核糖体蛋白类别。对当前数据库的搜索未能在已知的细菌或真核细胞质核糖体蛋白中发现任何同源物。然而,在Mrp10p与先前被鉴定为酵母线粒体50 S核糖体亚基组成部分的Yml37p之间检测到了一些序列相似性。