Nagata S, Tsunetsugu-Yokota Y, Naito A, Kaziro Y
Proc Natl Acad Sci U S A. 1983 Oct;80(20):6192-6. doi: 10.1073/pnas.80.20.6192.
A 3.1-kilobase Bgl II fragment of Saccharomyces cerevisiae carrying the nuclear gene encoding the mitochondrial polypeptide chain elongation factor (EF) Tu has been cloned on pBR327 to yield a chimeric plasmid pYYB. The identification of the gene designated as tufM was based on the cross-hybridization with the Escherichia coli tufB gene, under low stringency conditions. The complete nucleotide sequence of the yeast tufM gene was established together with its 5'- and 3'-flanking regions. The sequence contained 1,311 nucleotides coding for a protein of 437 amino acids with a calculated Mr of 47,980. The nucleotide sequence and the deduced amino acid sequence of tufM were 60% and 66% homologous, respectively, to the corresponding sequences of E. coli tufA, when aligned to obtain the maximal homology. Plasmid YRpYB was then constructed by cloning the 2.5-kilobase EcoRI fragment of pYYB carrying tufM into a yeast cloning vector YRp-7. A mRNA hybridizable with tufM was isolated from the total mRNA of S. cerevisiae D13-1A transformed with YRpYB and translated in the reticulocyte lysate. The mRNA could direct the synthesis of a protein with Mr 48,000, which was immunoprecipitated with an anti-E. coli EF-Tu antibody but not with an antibody against yeast cytoplasmic EF-1 alpha. The results indicate that the tufM gene is a nuclear gene coding for the yeast mitochondrial EF-Tu.
携带编码线粒体多肽链延伸因子(EF)Tu的核基因的酿酒酵母3.1千碱基Bgl II片段已克隆到pBR327上,产生嵌合质粒pYYB。在低严格条件下,通过与大肠杆菌tufB基因的交叉杂交确定了命名为tufM的基因。确定了酵母tufM基因及其5'和3'侧翼区域的完整核苷酸序列。该序列包含1311个核苷酸,编码一个437个氨基酸的蛋白质,计算的Mr为47980。当进行比对以获得最大同源性时,tufM的核苷酸序列和推导的氨基酸序列分别与大肠杆菌tufA的相应序列有60%和66%的同源性。然后通过将携带tufM的pYYB的2.5千碱基EcoRI片段克隆到酵母克隆载体YRp-7中构建质粒YRpYB。从用YRpYB转化的酿酒酵母D13-1A的总mRNA中分离出与tufM可杂交的mRNA,并在网织红细胞裂解物中进行翻译。该mRNA可指导合成一个Mr为48000的蛋白质,该蛋白质能用抗大肠杆菌EF-Tu抗体进行免疫沉淀,但不能用抗酵母细胞质EF-1α抗体进行免疫沉淀。结果表明,tufM基因是编码酵母线粒体EF-Tu的核基因。