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酿酒酵母的DNA修复基因:通过无法在大肠杆菌中复制的质粒对rad4和rev2突变进行互补。

DNA repair genes of Saccharomyces cerevisiae: complementing rad4 and rev2 mutations by plasmids which cannot be propagated in Escherichia coli.

作者信息

Siede W, Eckardt-Schupp F

机构信息

Gesellschaft für Strahlen- und Umweltforschung, Institut für Strahlenbiologie, Neuherberg, Federal Republic of Germany.

出版信息

Curr Genet. 1986;11(3):205-10. doi: 10.1007/BF00420608.

Abstract

The RAD4 gene of yeast required for the incision step of DNA excision repair and the REV2 (= RAD5) gene involved in mutagenic DNA repair could not be isolated from genomic libraries propagated in E. coli regardless of copy number of the shuttle vector in yeast. Transformants with plasmids conferring UV resistance to a rad4-4 or a rev2-1 mutant were only recovered if yeast was transformed directly without previous amplification of the gene bank in E. coli. DNA preparations from these yeast clones yielded no transformants in E. coli but retransformation of yeast was possible. This lead to the isolation of a defective derivative of the rad4 complementing plasmid. The modified plasmid was now capable of transforming E. coli but still interfered significantly with its growth.

摘要

酵母中DNA切除修复切口步骤所需的RAD4基因以及参与诱变DNA修复的REV2(=RAD5)基因,无论穿梭载体在酵母中的拷贝数如何,都无法从在大肠杆菌中繁殖的基因组文库中分离出来。只有在不事先在大肠杆菌中扩增基因文库而直接转化酵母的情况下,才能获得赋予rad4-4或rev2-1突变体紫外线抗性的质粒转化体。这些酵母克隆的DNA制备物在大肠杆菌中未产生转化体,但酵母的再次转化是可能的。这导致分离出rad4互补质粒的缺陷衍生物。现在,修饰后的质粒能够转化大肠杆菌,但仍对其生长有显著干扰。

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