Pretel R, Lennon K, Bird A, Kukuruzinska M A
Department of Oral Biology, Boston University Medical Center, Massachusetts 02118, USA.
Exp Cell Res. 1995 Aug;219(2):477-86. doi: 10.1006/excr.1995.1255.
The Saccharomyces cerevisiae ALG7 gene, which functions by initiating the dolichol pathway of protein N-glycosylation, displays properties of an early growth-response gene. To initiate studies of the involvement of ALG7 in cellular proliferation, we have now more precisely analyzed ALG7 expression in the G1 phase of cell cycle. We show that the rapid rate of ALG7 mRNA accumulation following growth stimulation was attenuated soon thereafter and that ALG7 growth induction occurred irrespective of alpha-factor. ALG7 growth induction was observed in mutants conditionally defective for reentry into the cell cycle from the stationary phase, indicating that the induction occurred prior to the performance of START. In addition, the steady-state levels of ALG7 mRNAs declined four-fold in response to START-I cell division arrest brought about by alpha-factor treatment later in G1. Importantly, deregulated expression of ALG7 resulted in an aberrant alpha-factor response. Our data not only indicate that ALG7 expression is regulated at two critical control points in G1 that determine the proliferative potential of cells, but also provide a link between ALG7 and START.
酿酒酵母ALG7基因通过启动蛋白质N-糖基化的多萜醇途径发挥作用,具有早期生长反应基因的特性。为了开始研究ALG7在细胞增殖中的作用,我们现在更精确地分析了细胞周期G1期的ALG7表达。我们发现,生长刺激后ALG7 mRNA的快速积累随后很快减弱,并且ALG7的生长诱导与α因子无关。在从静止期重新进入细胞周期存在条件缺陷的突变体中观察到了ALG7的生长诱导,这表明诱导发生在START执行之前。此外,由于在G1期后期用α因子处理导致START-I细胞分裂停滞,ALG7 mRNA的稳态水平下降了四倍。重要的是,ALG7的失控表达导致了异常的α因子反应。我们的数据不仅表明ALG7的表达在G1期的两个关键控制点受到调节,这两个控制点决定了细胞的增殖潜力,而且还提供了ALG7与START之间的联系。