Whiteway M, Dignard D, Thomas D Y
Eukaryotic Genetics Group, National Research Council of Canada, Montréal, Québec.
Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9410-4. doi: 10.1073/pnas.89.20.9410.
We have used a genomic library of Candida albicans to transform Saccharomyces cerevisiae and screened for genes that act similarly to dominant negative mutations by interfering with pheromone-mediated cell cycle arrest. Six different plasmids were identified from 2000 transformants; four have been sequenced. One gene (CZF1) encodes a protein with structural motifs characteristic of a transcription factor. A second gene (CCN1) encodes a cyclin homologue, a third (CRL1) encodes a protein with sequence similarity to GTP-binding proteins of the RHO family, and a fourth (CEK1) encodes a putative kinase of the ERK family. Since CEK1 confers a phenotype similar to that of the structurally related S. cerevisiae gene KSS1 but cannot complement a KSS1 defect, it is evident that dominant negative selection can identify proteins that complementation screens would miss. Because dominant negative mutations exert their influence even in wild-type strain backgrounds, this approach should be a general method for the analysis of complex cellular processes in organisms not amenable to direct genetic analysis.
我们利用白色念珠菌的基因组文库转化酿酒酵母,并筛选那些通过干扰信息素介导的细胞周期停滞而表现出与显性负性突变类似作用的基因。从2000个转化体中鉴定出6种不同的质粒;其中4种已测序。一个基因(CZF1)编码一种具有转录因子特征性结构基序的蛋白质。第二个基因(CCN1)编码一种细胞周期蛋白同源物,第三个基因(CRL1)编码一种与RHO家族的GTP结合蛋白具有序列相似性的蛋白质,第四个基因(CEK1)编码一种假定的ERK家族激酶。由于CEK1赋予的表型与结构相关的酿酒酵母基因KSS1的表型相似,但不能弥补KSS1缺陷,显然显性负性选择能够识别互补筛选可能遗漏的蛋白质。因为显性负性突变即使在野生型菌株背景中也能发挥作用,所以这种方法应该是分析不适合直接进行遗传分析的生物体中复杂细胞过程的通用方法。