Neu R, Goffart S, Wolf K, Schäfer B
Institut für Biologie IV (Mikrobiologie) der Rheinisch-Westfälischen Technischen Hochschule Aachen, Germany.
Mol Gen Genet. 1998 May;258(4):389-96. doi: 10.1007/s004380050746.
In previous papers we have reported the characterisation of mitochondrial mutator mutants of Schizosaccharomzyces pombe. In contrast to nuclear mutator mutants known from other eucaryotes, this mutator phenotype correlates with mutations in an unassigned open reading frame (urf a) in the mitochondrial genome. Since an efficient biolistic transformation system for fission yeast mitochondria is not yet available, we relocated the mitochondrial urf a gene to the nucleus. As host strain for the ectopic expression, we used the nonsense mutant ana(r)-6, which carries a premature stop codon in the urf a gene. The phenotype of this mutant is characterised by continuous segregation of progeny giving rise to fully respiration competent colonies, colonies that show moderate growth on glycerol and a fraction of colonies that are unable to grow on glycerol. The phenotype of this mutant provides an excellent tool with which to study the effects on the mutator phenotype of ectopic expression of the urf a gene. Since a UGA codon encoding tryptophan is present in the original mitochondrial gene, we constructed two types of expression cassettes containing either the mitochondrial version of the urf a gene (mt-urf a) or a standard genetic code version (nc-urf a; UGA replaced by UGG) fused to the N-terminal import leader sequence of the cox4 gene of Saccharomyces cerevisiae. We show that the expression of the mt-urf a gene in its new location is able to cure, at least in part, the phenotype of mutant ana(r)-6, whereas the expression of the nc-urf a gene completely restores the wild-type (non-mutator) phenotype. The significant similarity of the urf a gene to the mitochondrial var1 gene of S. cerevisiae and homologous genes in other yeasts suggests that the urf a gene product might be a ribosomal protein with a dual function in protein synthesis and maintenance of mitochondrial DNA integrity.
在之前的论文中,我们报道了粟酒裂殖酵母线粒体突变体的特征。与其他真核生物中已知的核突变体不同,这种突变体表型与线粒体基因组中一个未定位的开放阅读框(urf a)中的突变相关。由于尚未建立用于裂殖酵母线粒体的高效基因枪转化系统,我们将线粒体urf a基因转移到了细胞核中。作为异位表达的宿主菌株,我们使用了无义突变体ana(r)-6,它在urf a基因中携带一个提前的终止密码子。该突变体的表型特征是子代持续分离,产生完全具有呼吸能力的菌落、在甘油上生长适度的菌落以及一部分在甘油上无法生长的菌落。该突变体的表型提供了一个极好的工具,可用于研究urf a基因异位表达对突变体表型的影响。由于原始线粒体基因中存在编码色氨酸的UGA密码子,我们构建了两种类型的表达盒,分别包含与酿酒酵母cox4基因的N端导入前导序列融合的线粒体版本的urf a基因(mt-urf a)或标准遗传密码版本(nc-urf a;UGA被UGG取代)。我们表明,mt-urf a基因在其新位置的表达至少部分能够治愈突变体ana(r)-6的表型,而nc-urf a基因的表达则完全恢复野生型(非突变体)表型。urf a基因与酿酒酵母的线粒体var1基因以及其他酵母中的同源基因具有显著相似性,这表明urf a基因产物可能是一种核糖体蛋白,在蛋白质合成和线粒体DNA完整性维持方面具有双重功能。