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5’-Terminal AUGs in Escherichia coli mRNAs with Shine-Dalgarno Sequences: Identification and Analysis of Their Roles in Non-Canonical Translation Initiation

机译:具有Shine-Dalgarno序列的大肠杆菌mRNA中的5末端AUG:在非规范翻译起始中的鉴定和作用分析

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摘要

Analysis of the Escherichia coli transcriptome identified a unique subset of messenger RNAs (mRNAs) that contain a conventional untranslated leader and Shine-Dalgarno (SD) sequence upstream of the gene’s start codon while also containing an AUG triplet at the mRNA’s 5’- terminus (5’-uAUG). Fusion of the coding sequence specified by the 5’-terminal putative AUG start codon to a lacZ reporter gene, as well as primer extension inhibition assays, reveal that the majority of the 5’-terminal upstream open reading frames (5’-uORFs) tested support some level of lacZ translation, indicating that these mRNAs can function both as leaderless and canonical SD-leadered mRNAs. Although some of the uORFs were expressed at low levels, others were expressed at levels close to that of the respective downstream genes and as high as the naturally leaderless cI mRNA of bacteriophage λ. These 5’-terminal uORFs potentially encode peptides of varying lengths, but their functions, if any, are unknown. In an effort to determine whether expression from the 5’-terminal uORFs impact expression of the immediately downstream cistron, we examined expression from the downstream coding sequence after mutations were introduced that inhibit efficient 5’-uORF translation. These mutations were found to affect expression from the downstream cistrons to varying degrees, suggesting that some 5’-uORFs may play roles in downstream regulation. Since the 5’-uAUGs found on these conventionally leadered mRNAs can function to bind ribosomes and initiate translation, this indicates that canonical mRNAs containing 5’-uAUGs should be examined for their potential to function also as leaderless mRNAs.
机译:大肠杆菌转录组的分析确定了信使RNA(mRNA)的独特子集,该信使RNA(mRNA)在该基因起始密码子上游包含一个常规的非翻译前导序列和Shine-Dalgarno(SD)序列,同时在mRNA的5'-末端还包含一个AUG三联体( 5'-uAUG)。由5'-末端推定的AUG起始密码子指定的编码序列与lacZ报告基因的融合以及引物延伸抑制试验表明,大多数5'-末端上游开放阅读框(5'-uORF)被测试的蛋白支持一定水平的lacZ翻译,表明这些mRNA既可以充当无领导者,又可以作为标准的SD领导者mRNA。尽管某些uORF的表达水平很低,但其他uORF的表达水平却与相应下游基因的表达水平接近,并且与噬菌体λ的自然无前导cI mRNA一样高。这些5'端uORF可能编码长度不同的肽,但其功能(如果有)尚不清楚。为了确定5'-末端uORF的表达是否影响紧邻下游顺反子的表达,我们在引入抑制5'-uORF有效翻译的突变后检查了下游编码序列的表达。发现这些突变可不同程度地影响下游顺反子的表达,表明某些5'-uORF可能在下游调控中发挥作用。由于在这些传统的先导mRNA上发现的5'-uAUGs可以结合核糖体并启动翻译,因此,这表明应检查含有5'-uAUGs的规范性mRNAs发挥无导子mRNAs的潜力。

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