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Polyadenylation of a functional mRNA controls gene expression in Escherichia coli

机译:功能性mRNA的聚腺苷酸化控制大肠杆菌中的基因表达

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Although usually implicated in the stabilization of mRNAs in eukaryotes, polyadenylation was initially shown to destabilize RNA in bacteria. All the data are consistent with polyadenylation being part of a quality control process targeting folded RNA fragments and non-functional RNA molecules to degradation. We report here an example in Escherichia coli, where polyadenylation directly controls the level of expression of a gene by modulating the stability of a functional transcript. Inactivation of poly(A) polymerase I causes overexpression of glucosamine-6-phosphate synthase (GlmS) and both the accumulation and stabilization of the glmS transcript. Moreover, we show that the glmS mRNA results from the processing of the glmU-glmS cotranscript by RNase E. Interestingly, the glmU-glmS cotranscript and the mRNA fragment encoding GlmU only slightly accumulated in the absence of poly(A) polymerase, suggesting that the endonucleolytically generated glmS mRNA harbouring a 50 monophosphate and a 30 stable hairpin is highly susceptible to poly(A)-dependent degradation.
机译:尽管通常牵涉真核生物中mRNA的稳定化,但聚腺苷酸化最初显示出使细菌中的RNA不稳定。所有数据均与聚腺苷酸化一致,后者是针对折叠的RNA片段和非功能性RNA分子进行降解的质量控制过程的一部分。我们在这里报告一个大肠杆菌的例子,其中聚腺苷酸化通过调节功能性转录物的稳定性直接控制基因的表达水平。聚(A)聚合酶I的失活导致葡萄糖胺-6-磷酸合酶(GlmS)的过表达以及glmS转录物的积累和稳定。此外,我们显示glmS mRNA是由RNase E处理glmU-glmS共转录物而产生的。有趣的是,在不存在poly(A)聚合酶的情况下,glmU-glmS共转录物和编码GlmU的mRNA片段仅略有积累,这表明内切核酸生成的带有50个单磷酸和30个稳定发夹的glmS mRNA非常容易受到poly(A)依赖性降解的影响。

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