Rodriguez L, Lampen J O, MacKay V L
Waksman Institute of Microbiology, Rutgers University, Piscataway, New Jersey 08854.
Mol Cell Biol. 1981 May;1(5):469-74. doi: 10.1128/mcb.1.5.469-474.1981.
Saccharomyces cerevisiae revertant strain D10-ER1 has been shown to contain thermosensitive forms of the large (glycoprotein) and small (carbohydrate-free) invertases and a very low level of the small enzyme, along with a wild-type level of the large form (T. Mizunaga et al., Mol. Cell. Biol. 1:460-468, 1981). These characteristics cosegregated in crosses of the revertant strain with wild-type sucrose-fermenting (SUC1) or nonfermenting (suc0) strains. In addition, there is tight linkage between sucrose and maltose fermentation in revertant D10-ER1 (characteristic of the SUC1 and MAL1 genes). From this we infer that a single reversion event is responsible for the several changes observed in D10-ER1, and that this mutation maps within or very close to the SUC1 gene present in the ancestor strain 4059-358D. The revertant SUC1 allele in D10-ER1 (termed SUC1-R1) was expressed independently of the wild-type SUC1 gene when both were present in diploid cells. Diploids carrying only the wild-type or the mutant genes synthesized invertases with the characteristics of the parental Suc+ haploids. The possibility that a modifier gene was responsible for the alterations in the invertases of revertant D10-ER1 was ruled out by appropriate crosses. We conclude that SUC1 is a structural gene that codes for both the large and the small forms of invertase and suggest that SUC2 through SUC5 are structural genes as well.
酿酒酵母回复突变株D10 - ER1已被证明含有热敏形式的大(糖蛋白)和小(无糖)转化酶,以及极低水平的小酶,同时大形式的转化酶水平为野生型(T. Mizunaga等人,《分子细胞生物学》1:460 - 468,1981年)。这些特征在回复突变株与野生型蔗糖发酵(SUC1)或非发酵(suc0)菌株的杂交中共同分离。此外,回复突变株D10 - ER1中蔗糖和麦芽糖发酵之间存在紧密连锁(这是SUC1和MAL1基因的特征)。由此我们推断,单个回复事件导致了在D10 - ER1中观察到的几种变化,并且该突变位于祖先菌株4059 - 358D中存在的SUC1基因内部或非常接近该基因。当二倍体细胞中同时存在野生型SUC1基因和D10 - ER1中的回复突变SUC1等位基因(称为SUC1 - R1)时,SUC1 - R1独立表达。仅携带野生型或突变基因的二倍体合成具有亲本Suc +单倍体特征的转化酶。通过适当的杂交排除了修饰基因导致回复突变株D10 - ER1转化酶改变的可能性。我们得出结论,SUC1是一个结构基因,编码大、小两种形式的转化酶,并推测SUC2至SUC5也是结构基因。