Altboum Z, Gottlieb S, Lebens G A, Polacheck I, Segal E
Department of Microbiology, Israel Institute for Biological Research, Ness Ziona.
J Bacteriol. 1990 Jul;172(7):3898-904. doi: 10.1128/jb.172.7.3898-3904.1990.
Genetic studies were done with Candida albicans CBS 562. Various auxotrophs were isolated following mutagenesis with N-methyl-N'-nitro-N-nitrosoguanidine. SAG5 (his4C), a stable histidine auxotroph defective in histidinol dehydrogenase activity, was characterized and chosen for further molecular studies. Therefore, the C. albicans HIS4 gene was isolated. The gene was obtained from a genomic library of the wild-type strain, which was constructed in plasmid YEp24. The HIS4 gene was isolated by transformation of a Saccharomyces cerevisiae strain that carried a his4 mutation. The isolated C. albicans HIS4 gene complemented S. cerevisiae his4A, his4B, his4C, and his4ABC mutant strains, which indicates that the clone contains the entire HIS4 gene. The gene was isolated on plasmid pSTC7, whose physical map was constructed with BamHI, SalI, and EcoRV restriction endonucleases, locating the HIS4 gene on a 14-kilobase-pair DNA fragment. Hybridization experiments with HIS4 and C. albicans genomic DNA showed correspondence between the restriction patterns of the gene with that of the chromosomal DNA, indicating that the gene originates from C. albicans and appears in a single copy. Chromosomes of C. albicans CBS562 and four other strains were resolved by orthogonal-field alteration gel electrophoresis. The electrokaryotyping results showed heterogeneity in chromosomal sizes. The electrokaryotyping of CBS 562 showed a resolution of six chromosomal bands, three of which seemed to be doublets. The C. albicans HIS4 gene was located on the largest resolvable chromosome in all of the strains.
对白色念珠菌CBS 562进行了遗传学研究。用N-甲基-N'-硝基-N-亚硝基胍诱变后分离出各种营养缺陷型菌株。SAG5(his4C)是一种稳定的组氨酸营养缺陷型菌株,其组氨醇脱氢酶活性有缺陷,对其进行了特性鉴定并选择用于进一步的分子研究。因此,分离出了白色念珠菌HIS4基因。该基因从野生型菌株的基因组文库中获得,该文库构建于质粒YEp24中。通过转化携带his4突变的酿酒酵母菌株分离出HIS4基因。分离出的白色念珠菌HIS4基因互补了酿酒酵母his4A、his4B、his4C和his4ABC突变菌株,这表明该克隆包含完整的HIS4基因。该基因在质粒pSTC7上分离得到,用BamHI、SalI和EcoRV限制性内切酶构建了其物理图谱,将HIS4基因定位在一个14千碱基对的DNA片段上。用HIS4与白色念珠菌基因组DNA进行杂交实验,结果表明该基因的限制性图谱与染色体DNA的限制性图谱一致,表明该基因源自白色念珠菌且以单拷贝形式存在。通过正交场交变凝胶电泳解析了白色念珠菌CBS562和其他四个菌株的染色体。电泳核型分析结果显示染色体大小存在异质性。CBS 562的电泳核型分析显示有六条染色体带,其中三条似乎是双条带。在所有菌株中,白色念珠菌HIS4基因都位于最大的可分辨染色体上。