Wilson K L, Herskowitz I
Mol Cell Biol. 1984 Nov;4(11):2420-7. doi: 10.1128/mcb.4.11.2420-2427.1984.
The alpha 2 product of the alpha mating type locus of Saccharomyces cerevisiae is proposed to be a negative regulator of a set of dispersed genes concerned with specialized properties of a cells. This set of genes includes those, termed a-specific STE genes (STE2, STE6, and STE14), which are required for mating by a cells but not by alpha cells. We cloned the STE6 gene to determine whether its expression is limited to a cells and, if so, whether its expression is inhibited in alpha cells by the alpha 2 product. Expression of STE6 was assayed in two ways: by blot hybridization, RNA and by beta-galactosidase activity in strains carrying a STE6-lacZ hybrid gene. We found that STE6 expression was limited to a cells and was negatively regulated by the alpha 2 product. STE6 RNA was not detectable in strains containing the wild-type alpha 2 gene product. Expression of STE6 was at least 150-fold lower in alpha cells than in a cells, based on beta-galactosidase activities in a and alpha cells carrying the STE6-lacZ gene. These results confirmed that the alpha 2 product is a negative regulator of gene expression and showed that it acts at the level of RNA production. We also examined the phenotype of a mutant carrying an insertion mutation of the STE6 gene, the ste6::lacZ allele. In addition, an a-specific defect in mating, this mutant was greatly reduced (but not completely deficient) in a-factor production. Other phenotypes characteristic of a cells--Barrier activity, agglutination, and response to alpha-factor--were normal. STE6 thus appears to be necessary for biosynthesis of a-factor.
酿酒酵母α交配型位点的α2产物被认为是一组与α细胞特殊特性相关的分散基因的负调控因子。这组基因包括那些被称为α特异性STE基因(STE2、STE6和STE14)的基因,它们是α细胞交配所必需的,而α细胞则不需要。我们克隆了STE6基因,以确定其表达是否仅限于α细胞,如果是,其表达在α细胞中是否受到α2产物的抑制。通过两种方式检测STE6的表达:通过印迹杂交检测RNA,以及通过携带STE6 - lacZ杂交基因的菌株中的β - 半乳糖苷酶活性进行检测。我们发现STE6的表达仅限于α细胞,并且受到α2产物的负调控。在含有野生型α2基因产物的菌株中检测不到STE6 RNA。根据携带STE6 - lacZ基因的α细胞和α细胞中的β - 半乳糖苷酶活性,STE6在α细胞中的表达比在α细胞中至少低150倍。这些结果证实了α2产物是基因表达的负调控因子,并表明它在RNA产生水平上起作用。我们还研究了携带STE6基因插入突变(ste6::lacZ等位基因)的突变体的表型。除了α细胞交配方面的特异性缺陷外,该突变体在α因子产生方面大幅减少(但并非完全缺乏)。α细胞的其他特征性表型——屏障活性、凝集以及对α因子的反应——均正常。因此,STE6似乎是α因子生物合成所必需的。