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酿酒酵母中调控基因GAL80的破坏:对半乳糖/蜜二糖途径基因碳控制调节的影响。

Disruption of regulatory gene GAL80 in Saccharomyces cerevisiae: effects on carbon-controlled regulation of the galactose/melibiose pathway genes.

作者信息

Torchia T E, Hamilton R W, Cano C L, Hopper J E

出版信息

Mol Cell Biol. 1984 Aug;4(8):1521-7. doi: 10.1128/mcb.4.8.1521-1527.1984.

DOI:10.1128/mcb.4.8.1521-1527.1984
PMID:6092916
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC368943/
Abstract

In Saccharomyces cerevisiae, the transcriptional expression of the galactose-melibiose catabolic pathway genes is under the control of at least three regulatory genes, GAL4, GAL80, and GAL3. We have isolated the GAL80 gene and have studied the effect of a null mutation on the carbon-controlled regulation of the MEL1 and GAL cluster genes. The null mutation was achieved in vivo by replacing the chromosomal wild-type GAL80 allele with an in vitro-created GAL80 deletion-disruption mutation. Enzyme activities and RNA levels for the GAL cluster and MEL1 genes were constitutively expressed in the null mutant strain grown on glycerol-lactate and were higher than in the isogenic wild-type yeast strain when compared after growth on galactose. Carbon catabolite repression of the GAL cluster and MEL1 genes, which occurs at the level of transcription, is retained in the null mutant. Deletion of the GAL80 gene in a gal4 cell does not restore GAL cluster and MEL1 gene expression. The data demonstrate that (i) the GAL80 protein is a purely negative regulator, (ii) the GAL80 protein does not mediate carbon catabolite repression, and (iii) the GAL4 protein is not simply an antagonizer of GAL80-mediated repression.

摘要

在酿酒酵母中,半乳糖 - 蜜二糖分解代谢途径基因的转录表达受至少三个调控基因GAL4、GAL80和GAL3的控制。我们分离出了GAL80基因,并研究了无效突变对MEL1和GAL基因簇碳调控的影响。通过用体外构建的GAL80缺失 - 破坏突变体取代染色体野生型GAL80等位基因,在体内实现了无效突变。在甘油 - 乳酸培养基上生长的无效突变体菌株中,GAL基因簇和MEL1基因的酶活性和RNA水平组成型表达,并且在半乳糖上生长后与同基因野生型酵母菌株相比更高。GAL基因簇和MEL1基因的碳分解代谢物阻遏发生在转录水平,在无效突变体中仍然存在。在gal4细胞中缺失GAL80基因并不能恢复GAL基因簇和MEL1基因的表达。这些数据表明:(i)GAL80蛋白是一种纯粹的负调控因子;(ii)GAL80蛋白不介导碳分解代谢物阻遏;(iii)GAL4蛋白不仅仅是GAL80介导的阻遏的拮抗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcf/368943/fa45679c2b47/molcellb00150-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcf/368943/a30bc3a0d39a/molcellb00150-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcf/368943/9ad466ed4836/molcellb00150-0104-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcf/368943/fa45679c2b47/molcellb00150-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcf/368943/a30bc3a0d39a/molcellb00150-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcf/368943/9ad466ed4836/molcellb00150-0104-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcf/368943/fa45679c2b47/molcellb00150-0105-a.jpg

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