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A Saccharomyces cerevisiae UAS element controlled by protein kinase A activates transcription in response to a variety of stress conditions.

机译:由蛋白激酶A控制的酿酒酵母UAS元件响应于多种应激条件而激活转录。

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摘要

Transcription of the Saccharomyces cerevisiae CTT1 gene encoding the cytosolic catalase T is activated by a variety of stress conditions: it is derepressed by nitrogen starvation and induced by heat shock. Furthermore, it is activated by osmotic and oxidative stress. This study shows that a CTT1 upstream region previously found to be involved in nitrogen, cAMP and heat control (base pairs -382 to -325) contains a UAS element (STRE, -368 to -356), which is sufficient for the activation of a reporter gene by all types of stress acting on CTT1. Gel retardation experiments demonstrated the existence of a factor specifically binding to STRE, but to a lesser extent to mutated elements having partly or entirely lost the ability to mediate stress control. Heat activation of STRE, but not of a canonical heat shock element, is enhanced by a ras2 defect mutation, which enhances thermotolerance, and is dramatically reduced by a bcy1 disruption mutation, which decreases thermotolerance. It can be hypothesized, therefore, that the novel stress control element is important for the establishment of induced stress tolerance.
机译:酿酒酵母CTT1基因的转录编码胞质过氧化氢酶T被多种应激条件所激活:氮饥饿使其抑制并由热激诱导。此外,它被渗透和氧化应激激活。这项研究表明,先前发现参与氮,cAMP和热控制(碱基对-382至-325)的CTT1上游区域包含一个UAS元素(STRE,-368至-356),足以激活CTT1。各种压力作用于CTT1的报告基因。凝胶阻滞实验证明存在与STRE特异性结合的因子,但对部分或完全丧失介导压力控制能力的突变元素的结合程度较小。 ras2缺陷突变增强了STRE的热激活,但典范的热激元件则没有,因此增强了耐热性,而bcy1破坏突变显着降低了STRE的热激活,而bcy1破坏突变降低了耐热性。因此,可以假设,新颖的应力控制元件对于建立诱导的应力耐受性是重要的。

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