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首页> 外文期刊>Nucleic Acids Research >Comparative genomic analysis of translation initiation mechanisms for genes lacking the Shine-Dalgarno sequence in prokaryotes
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Comparative genomic analysis of translation initiation mechanisms for genes lacking the Shine-Dalgarno sequence in prokaryotes

机译:缺乏原基中缺乏Shine-Dalgarno序列的基因翻译起始机制的比较基因组分析

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In prokaryotes, translation initiation is believed to occur through an interaction between the 3' tail of a 16S rRNA and a corresponding Shine-Dalgarno (SD) sequence in the 5' untranslated region (UTR) of an mRNA. However, some genes lack SD sequences (non-SD genes), and the fraction of non-SD genes in a genome varies depending on the prokaryotic species. To elucidate non-SD translation initiation mechanisms in prokaryotes from an evolutionary perspective, we statistically examined the nucleotide frequencies around the initiation codons in non-SD genes from 260 prokaryotes (235 bacteria and 25 archaea). We identified distinct nucleotide frequency biases upstream of the initiation codon in bacteria and archaea, likely because of the presence of leaderless mRNAs lacking a 5' UTR. Moreover, we observed overall similarities in the nucleotide patterns between upstream and downstream regions of the initiation codon in all examined phyla. Symmetric nucleotide frequency biases might facilitate translation initiation by preventing the formation of secondary structures around the initiation codon. These features are more prominent in species' genomes that harbor large fractions of non-SD sequences, suggesting that a reduced stability around the initiation codon is important for efficient translation initiation in prokaryotes.
机译:在原核生物中,据信通过16S rRNA的3'尾部的相互作用和mRNA的5'未翻译区域(UTR)中的3'尾部的相互作用相互作用。然而,一些基因缺乏SD序列(非SD基因),并且基因组中的非SD基因的级分根据原核物种而变化。为了从进化的角度来阐明原核生物中的非SD翻译起始机制,我们在260个原核生物(235个细菌和25个古亚eA)中,统计研究了非SD基因的初始核苷酸频率。我们在细菌和古亚亚群中鉴定了初始核苷酸上游的不同的核苷酸频率偏差,可能是由于不含5英尺UTR的无领导MRNA的存在。此外,我们观察到在所有检查的植物中引发密码子的上游和下游区域之间的核苷酸模式中的总体相似性。对称核苷酸频率偏置可以通过防止在发起密码子周围形成二次结构来促进翻译开始。这些特征在物种的基因组中更加突出,这些特征在涉及大部分非SD序列的物种的基因组中,表明引发密码子周围的稳定性降低对于在原核生物中有效的翻译开始是重要的。

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