Cross F R, Tinkelenberg A H
Rockefeller University, New York, New York 10021.
Cell. 1991 May 31;65(5):875-83. doi: 10.1016/0092-8674(91)90394-e.
The CLN1, CLN2, and CLN3 genes of S. cerevisiae form a redundant family essential for the G1-to-S phase transition. CLN1 and CLN2 mRNAs were previously shown to be negatively regulated by mating pheromone and by cell cycle progression out of G1, whereas CLN3 mRNA is not. The CLN3-2 (DAF1-1) allele prevents both cell cycle arrest and the turnoff of CLN1 and CLN2 mRNAs in response to mating pheromone, but only in the presence of an active CDC28 gene. An internally deleted nonfunctional cln2 gene was used as a reporter gene to demonstrate that in the absence of mating pheromone, efficient expression of cln2 mRNA requires both an active CDC28 gene and at least one functional CLN gene. mRNA from a nonfunctional cln1 gene was regulated similarly. Thus, CLN function and CDC28 activity jointly stimulate CLN1 and CLN2 mRNA levels, potentially forming a positive feedback loop for CLN1 and CLN2 expression.
酿酒酵母的CLN1、CLN2和CLN3基因形成了一个对G1期到S期转换至关重要的冗余家族。先前研究表明,CLN1和CLN2 mRNA受交配信息素以及G1期之后的细胞周期进程的负调控,而CLN3 mRNA则不受此调控。CLN3-2(DAF1-1)等位基因可防止细胞周期停滞以及CLN1和CLN2 mRNA因交配信息素而关闭,但这仅在存在活性CDC28基因的情况下发生。一个内部缺失的无功能cln2基因被用作报告基因,以证明在不存在交配信息素的情况下,cln2 mRNA的有效表达既需要活性CDC28基因,也需要至少一个功能性CLN基因。来自无功能cln1基因的mRNA也受到类似的调控。因此,CLN功能和CDC28活性共同刺激CLN1和CLN2 mRNA水平,可能形成CLN1和CLN2表达的正反馈回路。