Landrieu I, Vandenbol M, Leberman R, Portetelle D, Hartlein M
Unité de Microbiologie, Faculté Universitaire des Sciences Agronomiques de Gembloux, Belgium.
Yeast. 1998 Apr 30;14(6):527-33. doi: 10.1002/(SICI)1097-0061(19980430)14:6<527::AID-YEA253>3.0.CO;2-3.
Exploiting the asparagine auxotrophy of the Saccharomyces cerevisiae mutant strain 8556a, we have isolated the gene for the cytosolic asparaginyl-tRNA synthetase (AsnRS) of S. cerevisiae, by functional complementation of the mutation affecting this strain. The isolated gene could be identified to the open reading frame YHR019, called DED81, located on chromosome VIII. The mutant gene from the 8556a strain, asnrs-1, was amplified from genomic DNA by PCR. This gene contains a point mutation, leading to the replacement of a glycine residue by a serine in a region of the protein probably important for the asparaginyl-adenylate recognition. The protein encoded by YHR019 is very similar to cytosolic AsnRS from other eukaryotic sources. In a phylogenetic analysis based on AsnRS sequences from various organisms, the eukaryotic sequences were clustered. Expression of YHR019 in Escherichia coli demonstrated that a yeast AsnRS activity was produced. The recombinant enzyme was purified to homogeneity in three chromatography steps. We showed that the recombinant S. cerevisiae AsnRS was able to charge unfractionated yeast tRNA, but not E. coli tRNA, with asparagine.
利用酿酒酵母突变株8556a的天冬酰胺营养缺陷型,我们通过对影响该菌株的突变进行功能互补,分离出了酿酒酵母胞质天冬酰胺-tRNA合成酶(AsnRS)的基因。分离出的基因可被鉴定为位于第八条染色体上的开放阅读框YHR019,称为DED81。通过PCR从基因组DNA中扩增出8556a菌株的突变基因asnrs-1。该基因包含一个点突变,导致蛋白质中一个可能对天冬酰胺-腺苷酸识别很重要的区域中的甘氨酸残基被丝氨酸取代。YHR019编码的蛋白质与来自其他真核生物的胞质AsnRS非常相似。在基于各种生物体AsnRS序列的系统发育分析中,真核生物序列聚类在一起。YHR019在大肠杆菌中的表达表明产生了酵母AsnRS活性。重组酶通过三步色谱法纯化至同质。我们表明,重组酿酒酵母AsnRS能够用天冬酰胺对未分级的酵母tRNA进行氨酰化,但不能对大肠杆菌tRNA进行氨酰化。