Ludmerer S W, Schimmel P
J Bacteriol. 1985 Aug;163(2):763-8. doi: 10.1128/jb.163.2.763-768.1985.
The structural gene for glutaminyl-tRNA synthetase has been isolated from a gene bank of Saccharomyces cerevisiae chromosomal DNA. Cloning was achieved by complementation of a recently described yeast strain that is auxotrophic for glutamine. A multicopy recombinant plasmid with a 5-kilobase-pair genomic insert conferred sixfold elevation in glutaminyl-tRNA synthetase activity and restored a Gln+ phenotype to strains that were Gln- by virtue of a mutant gln4 allele. Subfragments of the 5-kilobase insert directed integration of URA3 to GLN4. Further experiments established that GLN4 is an essential gene that is located on chromosome XV. RNA blots with a GLN4-specific probe detected a single transcript of approximately 2,900 nucleotides.
谷氨酰胺-tRNA合成酶的结构基因已从酿酒酵母染色体DNA基因文库中分离出来。通过对最近描述的对谷氨酰胺营养缺陷的酵母菌株进行互补来实现克隆。一个带有5千碱基对基因组插入片段的多拷贝重组质粒使谷氨酰胺-tRNA合成酶活性提高了六倍,并使因gln4突变等位基因而谷氨酰胺缺陷的菌株恢复了谷氨酰胺+表型。5千碱基插入片段的亚片段将URA3定向整合到GLN4。进一步的实验确定GLN4是一个位于第十五号染色体上的必需基因。用GLN4特异性探针进行的RNA印迹检测到一个约2900个核苷酸的单一转录本。