Nagata S, Nagashima K, Tsunetsugu-Yokota Y, Fujimura K, Miyazaki M, Kaziro Y
EMBO J. 1984 Aug;3(8):1825-30. doi: 10.1002/j.1460-2075.1984.tb02053.x.
Messenger RNA for yeast cytosolic polypeptide chain elongation factor 1 alpha (EF-1 alpha) was partially purified from Saccharomyces cerevisiae. Double-stranded complementary DNA (cDNA) was synthesized and cloned in Escherichia coli with pBR327 as a vector. Recombinant plasmid carrying yEF-1 alpha cDNA was identified by cross-hybridization with the E. coli tufB gene and the yeast mitochondrial EF-Tu gene (tufM) under non-stringent conditions. A yeast gene library was then screened with the EF-1 alpha cDNA and several clones containing the chromosomal gene for EF-1 alpha were isolated. Restriction analysis of DNA fragments of these clones as well as the Southern hybridization of yeast genomic DNA with labelled EF-1 alpha cDNA indicated that there are two EF-1 alpha genes in S. cerevisiae. The nucleotide sequence of one of the two EF-1 alpha genes (designated as EF1 alpha A) was established together with its 5'- and 3'-flanking sequences. The sequence contained 1374 nucleotides coding for a protein of 458 amino acids with a calculated mol. wt. of 50 300. The derived amino acid sequence showed homologies of 31% and 32% with yeast mitochondrial EF-Tu and E. coli EF-Tu, respectively.
从酿酒酵母中部分纯化了酵母胞质多肽链延长因子1α(EF-1α)的信使核糖核酸。以pBR327为载体,合成双链互补脱氧核糖核酸(cDNA)并克隆于大肠杆菌中。在非严格条件下,通过与大肠杆菌tufB基因和酵母线粒体EF-Tu基因(tufM)的交叉杂交,鉴定出携带yEF-1α cDNA的重组质粒。然后用EF-1α cDNA筛选酵母基因文库,分离出几个含有EF-1α染色体基因的克隆。对这些克隆的DNA片段进行限制性分析,以及用标记的EF-1α cDNA对酵母基因组DNA进行Southern杂交,结果表明酿酒酵母中有两个EF-1α基因。确定了两个EF-1α基因之一(命名为EF1α A)的核苷酸序列及其5'和3'侧翼序列。该序列包含1374个核苷酸,编码一个由458个氨基酸组成的蛋白质,计算分子量为50300。推导的氨基酸序列与酵母线粒体EF-Tu和大肠杆菌EF-Tu的同源性分别为31%和32%。