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大肠杆菌中密码子的使用和信使 RNA 编码区与小 RNA 之间的模块相互作用。

Codon usage and modular interactions between messenger RNA coding regions and small RNAs in Escherichia coli.

机构信息

Centro de Biotecnología Acuícola, Departamento de Biología, Universidad de Santiago de Chile, Alameda 3363, 9170022, Estación Central, Chile.

Programa de Biología Celular y Molecular, Instituto de Ciencias Biomédicas, Facultad de Medicina Universidad de Chile. Independencia 1027, 8380453, Santiago, Chile.

出版信息

BMC Genomics. 2018 Sep 6;19(1):657. doi: 10.1186/s12864-018-5038-6.

Abstract

BACKGROUND

Small RNAs (sRNAs) are key regulators of gene expression in bacteria. In addition to modulating translation initiation, sRNAs can interact with mRNA coding regions to regulate mRNA stability and translation efficiency, enhancing or impeding progression of the ribosome along the mRNA. Since most amino acids are decoded by more than one codon (synonymous) we asked as to whether there is a codon bias in the interaction of sRNAs with coding regions of mRNAs. Therefore, we explored whether there are differences in codon usage or tRNA availability according to whether an mRNA is regulated by sRNAs or not. We also explored these parameters in the coding interaction regions in mRNAs. We focused our analysis on sRNAs that regulate multiple mRNAs.

RESULTS

We found differences in codon adaptation index and tRNA adaptation index between sRNA-regulated and non-sRNA-regulated mRNAs. Interestingly, the sRNA-mRNA interacting regions tended to be enriched in unpreferred codons decoded by scarce tRNAs. We also found that sRNAs with multiple targets often contained modular segments capable of recognizing conserved motifs among these mRNAs.

CONCLUSIONS

Our results show that sRNAs in E. coli tend to recognize mRNA coding regions in which the ribosome is predicted to advance at low speeds. Identified motifs in interacting regions are conserved among mRNAs that are recognized by the same sRNA.

摘要

背景

小分子 RNA(sRNAs)是细菌中基因表达的关键调节剂。除了调节翻译起始外,sRNAs 还可以与 mRNA 编码区相互作用,调节 mRNA 的稳定性和翻译效率,从而促进或阻碍核糖体在 mRNA 上的前进。由于大多数氨基酸都由不止一个密码子(同义密码子)编码,我们想知道 sRNA 与 mRNA 编码区的相互作用是否存在密码子偏好。因此,我们探讨了是否根据 mRNA 是否被 sRNA 调控,存在密码子使用或 tRNA 可用性的差异。我们还在 mRNA 的编码相互作用区域中探讨了这些参数。我们的分析重点放在调控多个 mRNA 的 sRNA 上。

结果

我们发现 sRNA 调控和非 sRNA 调控的 mRNA 在密码子适应指数和 tRNA 适应指数上存在差异。有趣的是,sRNA-mRNA 相互作用区域倾向于富含由稀有 tRNA 解码的非偏好密码子。我们还发现,具有多个靶标的 sRNAs 通常包含能够识别这些 mRNA 之间保守模体的模块化片段。

结论

我们的结果表明,大肠杆菌中的 sRNA 倾向于识别核糖体预测速度较慢的 mRNA 编码区。在被相同 sRNA 识别的相互作用区域中,鉴定出的基序在被识别的 mRNA 之间是保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeb4/6127932/2653986dce08/12864_2018_5038_Fig1_HTML.jpg

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