Liao H, Thorner J
Proc Natl Acad Sci U S A. 1980 Apr;77(4):1898-902. doi: 10.1073/pnas.77.4.1898.
The pheromone alpha factor, secreted by Saccharomyces cerevisiae cells of the alpha mating type, serves to synchronize the opposite mating type (a cells) at G1 as a prelude to fusion of the two cell types. We found that, in vitro, alpha factor inhibited the membrane-bound adenylate cyclase of these cells in a dose-dependent manner. Moreover, one class (ste5) of a cell mutants that grow normally at either 23 degrees or 34 degrees C but that are unable to respond to alpha factor or to mate at the higher temperature possessed an adenylate cyclase activity that was not inhibited by alpha factor at 34 degrees C but was fully sensitive to inhibition at 23 degrees C. Furthermore, addition of cyclic AMP to a cell culture medium shortened the period of pheromone-induced G1 arrest. We conclude that inhibition of adenylate cyclase activity by alpha factor may constitute, at least in part, the biochemical mode of action of the pheromone in vivo.
α交配型的酿酒酵母细胞分泌的信息素α因子,可使相反交配型(a细胞)在G1期同步,作为两种细胞类型融合的前奏。我们发现,在体外,α因子以剂量依赖的方式抑制这些细胞的膜结合腺苷酸环化酶。此外,一类(ste5)a细胞突变体在23℃或34℃下均能正常生长,但在较高温度下无法对α因子作出反应或进行交配,其腺苷酸环化酶活性在34℃时不受α因子抑制,但在23℃时对抑制作用完全敏感。此外,向a细胞培养基中添加环磷酸腺苷可缩短信息素诱导的G1期停滞时间。我们得出结论,α因子对腺苷酸环化酶活性的抑制可能至少部分构成了信息素在体内的生化作用模式。