Hori Y, Shirahige K, Obuse C, Tsurimoto T, Yoshikawa H
Department of Molecular Biology, Nara Institute of Science and Technology, Japan.
Mol Biol Cell. 1996 Mar;7(3):409-18. doi: 10.1091/mbc.7.3.409.
A novel cell cycle gene was identified by a computer search for genes partly homologous to known CDC genes, CDC6 of Saccharomyces cerevisiae and CDC18 of Schizosaccharomyces pombe, using the nucleotide sequence data base for S. cerevisiae produced by the Yeast Sequencing Project. The protein sequence coded by the cloned gene was found to be identical to that of purified ORC1 protein. Disruption of the gene and subsequent tetrad analysis revealed that the gene was essential for growth. The function of the gene product was analyzed by depleting the protein from the cell using a mutant haploid strain containing the disrupted ORC1 gene on the chromosome and a galactose-inducible gene coding for HA-tagged ORC1 protein on a single copy plasmid. The HA-tagged protein was expressed during growth in the presence of galactose but began to decrease rapidly upon depletion of galactose. Analysis of the cell cycle progression of the mutant cells by FACS after the removal of galactose from the medium, and microscope observations of cells and their nuclei revealed that the normal progression of 2N cells was immediately impeded as the ORC1 protein started to decrease. This was blocked completely in the cells that had progressed to the S phase under conditions deficient in ORC1 protein followed by cell death. Two-dimensional gel analysis of the replication intermediates after the galactose removal revealed that the depletion of ORC1 protein caused a decrease in the frequency of initiation of chromosomal replication, eventually resulting in the inhibition of replication as a whole. The function of the ORC1 protein in the cell cycle progression of S. cerevisiae is discussed in light of current information on ORC.
通过计算机搜索部分同源于已知CDC基因(酿酒酵母的CDC6和粟酒裂殖酵母的CDC18)的基因,利用酵母测序计划产生的酿酒酵母核苷酸序列数据库,鉴定出一个新的细胞周期基因。发现克隆基因编码的蛋白质序列与纯化的ORC1蛋白相同。该基因的破坏及随后的四分体分析表明该基因对生长至关重要。利用一个在染色体上含有破坏的ORC1基因的突变单倍体菌株和一个在单拷贝质粒上编码HA标签ORC1蛋白的半乳糖诱导基因,从细胞中去除该蛋白,分析该基因产物的功能。在半乳糖存在下生长期间表达HA标签蛋白,但在半乳糖耗尽后开始迅速减少。从培养基中去除半乳糖后,通过FACS分析突变细胞的细胞周期进程,以及对细胞及其细胞核的显微镜观察表明,随着ORC1蛋白开始减少,2N细胞的正常进程立即受到阻碍。在ORC1蛋白缺乏的条件下进入S期的细胞中,这一进程被完全阻断,随后细胞死亡。去除半乳糖后对复制中间体的二维凝胶分析表明,ORC1蛋白的耗尽导致染色体复制起始频率降低,最终导致整体复制受到抑制。根据关于ORC的当前信息,讨论了ORC1蛋白在酿酒酵母细胞周期进程中的功能。