Couto L B, Friedberg E C
Department of Pathology, Stanford University School of Medicine, California 94305.
J Bacteriol. 1989 Apr;171(4):1862-9. doi: 10.1128/jb.171.4.1862-1869.1989.
Shuttle plasmids carrying the wild-type RAD4 gene of Saccharomyces cerevisiae cannot be propagated in Escherichia coli (R. Fleer, W. Siede, and E. C. Friedberg, J. Bacteriol. 169:4884-4892, 1987). In order to determine the nucleotide sequence of the cloned gene, we used a plasmid carrying a mutant allele that allows plasmid propagation in E. coli. The wild-type sequence in the region of this mutation was determined from a second plasmid carrying a different mutant rad4 allele. We established the locations and characteristics of a number of spontaneously generated plasmid-borne RAD4 mutations that alleviate the toxicity of the wild-type gene in E. coli and of several mutagen-induced chromosomal mutations that inactivate the excision repair function of RAD4. These mutations are situated in very close proximity to each other, and all are expected to result in the expression of truncated polypeptides missing the carboxy-terminal one-third of the Rad4 polypeptide. This region of the gene may be important both for the toxic effect of the Rad4 protein in E. coli and for its role in DNA repair in S. cerevisiae.
携带酿酒酵母野生型RAD4基因的穿梭质粒无法在大肠杆菌中复制(R. 弗莱尔、W. 西德和E. C. 弗里德伯格,《细菌学杂志》169:4884 - 4892,1987年)。为了确定克隆基因的核苷酸序列,我们使用了携带一个突变等位基因的质粒,该等位基因允许质粒在大肠杆菌中复制。此突变区域的野生型序列是从携带不同rad4突变等位基因的第二个质粒中确定的。我们确定了一些自发产生的质粒携带的RAD4突变的位置和特征,这些突变减轻了野生型基因在大肠杆菌中的毒性,以及一些诱变诱导的染色体突变的位置和特征,这些突变使RAD4的切除修复功能失活。这些突变彼此位置非常接近,预计所有突变都会导致截短多肽的表达,这些多肽缺失了Rad4多肽羧基末端的三分之一。该基因的这一区域对于Rad4蛋白在大肠杆菌中的毒性作用及其在酿酒酵母DNA修复中的作用可能都很重要。