首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Molecular cloning and sequence determination of the nuclear gene coding for mitochondrial elongation factor Tu of Saccharomyces cerevisiae.
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Molecular cloning and sequence determination of the nuclear gene coding for mitochondrial elongation factor Tu of Saccharomyces cerevisiae.

机译:酿酒酵母线粒体延伸因子Tu的核基因的分子克隆和序列测定。

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摘要

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.
机译:已将携带编码线粒体多肽链延长因子(EF)Tu的核基因的啤酒酵母的3.1碱基对Bgl II片段克隆到pBR327上,以产生嵌合质粒pYYB。命名为tufM的基因的鉴定是基于在低严格条件下与大肠杆菌tufB基因的交叉杂交。建立了酵母tufM基因的完整核苷酸序列及其5'和3'侧翼区域。该序列包含1,311个核苷酸,编码437个氨基酸的蛋白质,Mr估计为47,980。当比对以获得最大的同源性时,tufM的核苷酸序列和推导的氨基酸序列分别与大肠杆菌tufA的相应序列同源60%和66%同源。然后通过将携带tufM的pYYB的2.5-碱基碱基的EcoRI片段克隆到酵母克隆载体YRp-7中来构建质粒YRpYB。从用YRpYB转化并在网织红细胞裂解物中翻译的酿酒酵母D13-1A的总mRNA中分离出可与tufM杂交的mRNA。 mRNA可以指导48,000先生的蛋白质合成,并用抗E进行免疫沉淀。大肠杆菌EF-Tu抗体,但不包含针对酵母胞质EF-1 alpha的抗体。结果表明,tufM基因是编码酵母线粒体EF-Tu的核基因。

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