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Regulation of conditional gene expression by coupled transcription repression and RNA degradation

机译:通过偶联转录抑制和RNA降解调节条件基因表达

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摘要

Gene expression is determined by a combination of transcriptional and post-transcriptional regulatory events that were thought to occur independently. This report demonstrates that the genes associated with the Snf3p–Rgt2p glucose-sensing pathway are regulated by interconnected transcription repression and RNA degradation. Deletion of the dsRNA-specific ribonuclease III Rnt1p increased the expression of Snf3p–Rgt2p-associated transcription factors in vivo and the recombinant enzyme degraded their messenger RNA in vitro. Surprisingly, Rnt1ps effect on gene expression in vivo was both RNA and promoter dependent, thus linking RNA degradation to transcription. Strikingly, deletion of RNT1-induced promoter-specific transcription of the glucose sensing genes even in the absence of RNA cleavage signals. Together, the results presented here support a model in which co-transcriptional RNA degradation increases the efficiency of gene repression, thereby allowing an effective cellular response to the continuous changes in nutrient concentrations.
机译:基因表达是由转录和转录后调控事件(被认为独立发生)的组合决定的。该报告表明,与Snf3p–Rgt2p葡萄糖感测途径相关的基因受到相互关联的转录抑制和RNA降解的调控。 dsRNA特异性核糖核酸酶III Rnt1p的缺失增加了体内Snf3p–Rgt2p相关转录因子的表达,重组酶在体外降解了其信使RNA。出人意料的是,Rnt1ps对体内基因表达的影响是RNA和启动子依赖性的,因此将RNA降解与转录联系起来。令人惊讶的是,即使没有RNA裂解信号,RNT1诱导的葡萄糖传感基因的启动子特异性转录的缺失。总之,这里给出的结果支持了一种模型,其中共转录RNA降解提高了基因阻抑的效率,从而允许对营养物浓度的连续变化进行有效的细胞反应。

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