Aebi M, Kirchner G, Chen J Y, Vijayraghavan U, Jacobson A, Martin N C, Abelson J
California Institute of Technology, Division of Biology, Pasadena 91125.
J Biol Chem. 1990 Sep 25;265(27):16216-20.
We have isolated a yeast mutant, ts352, that is temperature-sensitive for growth. The mutation has a general effect on mRNA metabolism and a specific effect on tRNA biosynthesis. Cells shifted to the nonpermissive temperature accumulate tRNAs that are shorter than mature tRNAs. The increased ability of these tRNAs to accept ATP demonstrates that growth of the ts352 mutant at the nonpermissive temperature results in accumulation of tRNA with defective 3' ends. The activity of ATP (CTP):tRNA-specific tRNA nucleotidyltransferase can readily be measured in extracts from wild type but not mutant cells. We have cloned and sequenced the wild type allele of the ts352 gene and find significant similarity between the yeast protein sequence predicted from the DNA sequence and the protein predicted from the sequence of the Escherichi coli tRNA nucleotidyltransferase gene. Expression of the yeast gene on a multicopy plasmid increases the activity of the tRNA nucleotidyltransferase in extracts. We conclude that the defect in the ts352 mutant is in the gene coding for yeast tRNA nucleotidyltransferase and that we have isolated the yeast gene that codes for this enzyme.
我们分离出了一种酵母突变体ts352,其生长对温度敏感。该突变对mRNA代谢有普遍影响,对tRNA生物合成有特定影响。转移到非允许温度的细胞会积累比成熟tRNA短的tRNA。这些tRNA接受ATP能力的增强表明,ts352突变体在非允许温度下生长会导致3'端有缺陷的tRNA积累。ATP(CTP):tRNA特异性tRNA核苷酸转移酶的活性可以很容易地在野生型细胞提取物中检测到,但在突变体细胞提取物中则检测不到。我们已经克隆并测序了ts352基因的野生型等位基因,发现从DNA序列预测的酵母蛋白序列与从大肠杆菌tRNA核苷酸转移酶基因序列预测的蛋白之间有显著的相似性。在多拷贝质粒上表达酵母基因会增加提取物中tRNA核苷酸转移酶的活性。我们得出结论,ts352突变体的缺陷在于编码酵母tRNA核苷酸转移酶的基因,并且我们已经分离出了编码这种酶的酵母基因。