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首页> 外文期刊>RNA >Inhibition of 5 ' to 3 ' mRNA degradation under stress conditions in Saccharomyces cerevisiae: from GCN4 to MET16
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Inhibition of 5 ' to 3 ' mRNA degradation under stress conditions in Saccharomyces cerevisiae: from GCN4 to MET16

机译:酿酒酵母在胁迫条件下5'至3'mRNA降解的抑制:从GCN4到MET16

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After deadenylation, most cytoplasmic mRNAs are decapped and digested by 5' to 3' exonucleases in Saccharomyces cerevisiae. Capped and deadenylated mRNAs are degraded to a lesser extent by 3' to 5' exonucleases. We have used a method, based on the electroporation of in vitro synthetised mRNAs, to study the relative importance of these two exonucleolytic pathways under stress conditions. We show that derepression of GCN4 upon amino acid starvation specifically limits the 5'-to-3'-degradation pathway. Because adenosine 3'-5' biphosphate (pAp), which is produced by Met16p, inhibits this degradation pathway to a comparable extent, we were prompted to analyse the role of Met16p in this phenomenon. We show that the inhibitory effects of amino acid limitation on 5' to 3' mRNA degradation are absent in a met16 mutant. We therefore conclude that the GCN4 dependence of MET16 expression is responsible for the decrease in 5' to 3' digestion under stress conditions and that cells use pAp as a signal to limit 5' to 3' RNA degradation under stress conditions. Because 3' to 5' mRNA degradation is unaffected, the relative importance of this pathway in the decay of certain RNAs may be increased under stress conditions. [References: 51]
机译:腺苷酸化后,在酿酒酵母中,大多数细胞质mRNA均被脱盖并被5'至3'核酸外切酶消化。 3'至5'核酸外切酶将加帽和去甲腺苷酸化的mRNA降解程度较小。我们已经使用了一种基于体外合成的mRNA的电穿孔的方法,来研究这两种核酸外切途径在压力条件下的相对重要性。我们表明,GCN4在氨基酸饥饿时的抑制作用特别限制了5'至3'降解途径。由于Met16p产生的3'-5'磷酸腺苷(pAp)在相当程度上抑制了该降解途径,因此提示我们分析Met16p在此现象中的作用。我们表明,在met16突变体中不存在氨基酸限制对5'至3'mRNA降解的抑制作用。因此,我们得出结论,MET16表达的GCN4依赖性是造成应激条件下5'至3'消化减少的原因,并且细胞利用pAp作为信号来限制应激条件下5'至3'RNA降解。由于3'至5'mRNA的降解不受影响,因此在胁迫条件下该途径在某些RNA降解中的相对重要性可能会增加。 [参考:51]

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