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参与酿酒酵母中碳源分解代谢物阻遏和去阻遏的新基因。

New genes involved in carbon catabolite repression and derepression in the yeast Saccharomyces cerevisiae.

作者信息

Entian K D, Zimmermann F K

出版信息

J Bacteriol. 1982 Sep;151(3):1123-8. doi: 10.1128/jb.151.3.1123-1128.1982.

Abstract

A mutation causing resistance to carbon catabolite repression in gene HEX2, mutant allele hex2-3, causes an extreme sensitivity to maltose when in combination with the genes necessary for maltose metabolism. This provided a convenient system for the selective isolation of mutations in genes specifically required for maltose metabolism and other genes involved in general carbon catabolite repression. In addition to reversion of the hex2-3 allele, mutations in three other genes were detected. These genes were called CAT1, CAT3, and MUR1 and in a mutated form abolished maltose inhibition caused by mutant allele hex2-3. Mutant alleles cat1 and cat3 also restored normal repression in the presence of the hex2-3 allele. Segregants having only mutant alleles cat1 or cat3 were obtained by tetrad analysis. These segregants could not grow on nonfermentable carbon sources. Mutant alleles of gene CAT1 were allelic to a mutant allele cat1-1 previously isolated (Zimmermann et al., Mol. Gen. Genet. 151:95-103). Such mutants prevented derepression not only of the maltose catabolizing system, the selected property, but also of glyoxylate shunt and gluconeogenic enzymes. However, respiratory activities and invertase formation were not affected under derepressing conditions. cat3 mutants had the same phenotypic properties as cat1 mutants. This showed that carbon metabolism in yeast cells is under a very complex and ramified control of repressing and derepressing genes, which are interdependent.

摘要

基因HEX2中的一个导致对碳分解代谢物阻遏产生抗性的突变,即突变等位基因hex2-3,当与麦芽糖代谢所需的基因结合时,会导致对麦芽糖极度敏感。这为选择性分离麦芽糖代谢特异性所需基因以及参与一般碳分解代谢物阻遏的其他基因中的突变提供了一个便利的系统。除了hex2-3等位基因的回复突变外,还检测到其他三个基因的突变。这些基因被称为CAT1、CAT3和MUR1,其突变形式消除了由突变等位基因hex2-3引起的麦芽糖抑制作用。突变等位基因cat1和cat3在存在hex2-3等位基因的情况下也恢复了正常的阻遏作用。通过四分体分析获得了仅具有突变等位基因cat1或cat3的分离子。这些分离子不能在不可发酵的碳源上生长。基因CAT1的突变等位基因与先前分离的突变等位基因cat1-1等位(齐默尔曼等人,《分子遗传学与普通遗传学》151:95-103)。此类突变体不仅阻止了所选特性即麦芽糖分解代谢系统的去阻遏,还阻止了乙醛酸循环和糖异生酶的去阻遏。然而,在去阻遏条件下呼吸活性和转化酶的形成不受影响。cat3突变体具有与cat1突变体相同的表型特性。这表明酵母细胞中的碳代谢受到抑制和去抑制基因的非常复杂且分支众多的控制,这些基因相互依赖。

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本文引用的文献

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