Rose M, Grisafi P, Botstein D
Gene. 1984 Jul-Aug;29(1-2):113-24. doi: 10.1016/0378-1119(84)90172-0.
The expression of the cloned Saccharomyces cerevisiae URA3 gene in Escherichia coli on both plasmid and phage vectors was studied. Isolates of the gene from two different laboratory strains of yeast differ in their ability to be expressed in E. coli in the absence of external adjacent promoters of transcription. The DNA sequence of the two genes was determined and revealed several differences in the DNA flanking the structural gene. One base change alters the "Pribnow-box" of an E. coli promoter present in the yeast sequences. Three amber alleles of the yeast gene were also cloned from yeast. Two of the alleles could be suppressed in E. coli by a tRNA suppressor mutation. One of the amber alleles was determined to be a mutation in the seventh codon of the structural gene, thereby establishing the reading frame and extent of the coding sequence. The initiator codon of the reading frame encoding the URA3 structural gene is preceded by two other ATG codons in a different reading frame 61 and 79 bp away. The nearer ATG begins an open reading frame that overlaps the structural gene sequences by 17 bp. With the DNA sequence of the URA3 gene many of the common yeast vector plasmids are now completely known at the level of DNA sequence.
研究了克隆的酿酒酵母URA3基因在大肠杆菌中于质粒和噬菌体载体上的表达情况。从两种不同实验室酵母菌株中分离得到的该基因,在没有外部相邻转录启动子的情况下,在大肠杆菌中的表达能力有所不同。测定了这两个基因的DNA序列,结果显示结构基因两侧的DNA存在若干差异。一个碱基变化改变了酵母序列中存在的大肠杆菌启动子的“Pribnow框”。还从酵母中克隆了该酵母基因的三个琥珀突变等位基因。其中两个等位基因在大肠杆菌中可被一种tRNA抑制突变所抑制。确定其中一个琥珀突变等位基因是结构基因第七个密码子中的突变,从而确定了编码序列的阅读框和范围。编码URA3结构基因的阅读框起始密码子之前,在不同阅读框中距离其61和79 bp处还有另外两个ATG密码子。较近的ATG起始一个与结构基因序列重叠17 bp的开放阅读框。有了URA3基因的DNA序列,现在许多常见的酵母载体质粒在DNA序列水平上已完全清楚。