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酵母中的葡萄糖阻遏

Glucose repression in yeast.

作者信息

Carlson M

机构信息

Departments of Genetics and Development and Microbiology, Columbia University, HHSC 922, Box 136, 701 W. 168th Street, New York, NY 10032, USA.

出版信息

Curr Opin Microbiol. 1999 Apr;2(2):202-7. doi: 10.1016/S1369-5274(99)80035-6.

DOI:10.1016/S1369-5274(99)80035-6
PMID:10322167
Abstract

The Snf1 protein kinase is a central component of the signaling pathway for glucose repression in yeast. Recent studies have addressed the regulation of Snf1 kinase activity and elucidated mechanisms by which Snf1 controls repression and activation of glucose-repressed genes. Important advances include evidence that Snf1 regulates the localization of the Mig1 repressor and that Snf1 functions at multiple points to control Cat8 and Sip4, the activators of gluconeogenic genes.

摘要

Snf1蛋白激酶是酵母中葡萄糖阻遏信号通路的核心组成部分。最近的研究探讨了Snf1激酶活性的调节,并阐明了Snf1控制葡萄糖阻遏基因的阻遏和激活的机制。重要进展包括有证据表明Snf1调节Mig1阻遏物的定位,以及Snf1在多个位点发挥作用以控制糖异生基因的激活剂Cat8和Sip4。

相似文献

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Glucose repression in yeast.酵母中的葡萄糖阻遏
Curr Opin Microbiol. 1999 Apr;2(2):202-7. doi: 10.1016/S1369-5274(99)80035-6.
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Glucose de-repression by yeast AMP-activated protein kinase SNF1 is controlled via at least two independent steps.酵母 AMP 激活的蛋白激酶 SNF1 通过至少两个独立的步骤实现葡萄糖去阻遏。
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Active Snf1 protein kinase inhibits expression of the Saccharomyces cerevisiae HXT1 glucose transporter gene.活性Snf1蛋白激酶抑制酿酒酵母HXT1葡萄糖转运蛋白基因的表达。
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Cat8 and Sip4 mediate regulated transcriptional activation of the yeast malate dehydrogenase gene MDH2 by three carbon source-responsive promoter elements.Cat8和Sip4通过三种碳源响应性启动子元件介导酵母苹果酸脱氢酶基因MDH2的调控转录激活。
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Sip4, a Snf1 kinase-dependent transcriptional activator, binds to the carbon source-responsive element of gluconeogenic genes.Sip4是一种依赖Snf1激酶的转录激活因子,它与糖异生基因的碳源响应元件结合。
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Physiological characterization of glucose repression in the strains with SNF1 and SNF4 genes deleted.缺失SNF1和SNF4基因的菌株中葡萄糖阻遏的生理学特征
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