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含铅和无铅基因结构对耻垢分枝杆菌翻译效率、转录本稳定性和预测转录率的影响。

The Impact of Leadered and Leaderless Gene Structures on Translation Efficiency, Transcript Stability, and Predicted Transcription Rates in Mycobacterium smegmatis.

机构信息

Department of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.

Department of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, Massachusetts, USA

出版信息

J Bacteriol. 2020 Apr 9;202(9). doi: 10.1128/JB.00746-19.

Abstract

Regulation of gene expression is critical for to tolerate stressors encountered during infection and for nonpathogenic mycobacteria such as to survive environmental stressors. Unlike better-studied models, mycobacteria express ∼14% of their genes as leaderless transcripts. However, the impacts of leaderless transcript structures on mRNA half-life and translation efficiency in mycobacteria have not been directly tested. For leadered transcripts, the contributions of 5' untranslated regions (UTRs) to mRNA half-life and translation efficiency are similarly unknown. In and , the essential sigma factor, SigA, is encoded by a transcript with a relatively short half-life. We hypothesized that the long 5' UTR of causes this instability. To test this, we constructed fluorescence reporters and measured protein abundance, mRNA abundance, and mRNA half-life and calculated relative transcript production rates. The 5' UTR conferred an increased transcript production rate, shorter mRNA half-life, and decreased apparent translation rate compared to a synthetic 5' UTR commonly used in mycobacterial expression plasmids. Leaderless transcripts appeared to be translated with similar efficiency as those with the 5' UTR but had lower predicted transcript production rates. A global comparison of mRNA and protein abundances failed to reveal systematic differences in protein/mRNA ratios for leadered and leaderless transcripts, suggesting that variability in translation efficiency is largely driven by factors other than leader status. Our data are also discussed in light of an alternative model that leads to different conclusions and suggests leaderless transcripts may indeed be translated less efficiently. Tuberculosis, caused by , is a major public health problem killing 1.5 million people globally each year. During infection, must alter its gene expression patterns to adapt to the stress conditions it encounters. Understanding how regulates gene expression may provide clues for ways to interfere with the bacterium's survival. Gene expression encompasses transcription, mRNA degradation, and translation. Here, we used as a model organism to study how 5' untranslated regions affect these three facets of gene expression in multiple ways. We furthermore provide insight into the expression of leaderless mRNAs, which lack 5' untranslated regions and are unusually prevalent in mycobacteria.

摘要

基因表达的调控对于应对感染期间遇到的应激源以及对于非致病性分枝杆菌(如 )在环境应激源下的存活至关重要。与研究更为充分的模型不同,分枝杆菌约有 14%的基因以无 5' 端引导序列的转录本形式表达。然而,无 5' 端引导序列转录本结构对分枝杆菌中 mRNA 半衰期和翻译效率的影响尚未被直接测试。对于有 5' 端引导序列的转录本,5' 非翻译区(UTR)对 mRNA 半衰期和翻译效率的贡献也同样未知。在 和 中,必需的 sigma 因子 SigA 由半衰期相对较短的转录本编码。我们假设 长的 5'UTR 导致了这种不稳定性。为了验证这一点,我们构建了荧光报告物并测量了蛋白丰度、mRNA 丰度、mRNA 半衰期和相对转录物产生率。与分枝杆菌表达质粒中常用的合成 5'UTR 相比, 5'UTR 赋予了更高的转录物产生率、更短的 mRNA 半衰期和更低的表观翻译速率。无 5' 端引导序列的转录本似乎以与有 5'UTR 的转录本相似的效率进行翻译,但预测的转录物产生率较低。对 mRNA 和蛋白丰度的全局比较未能揭示有 5' 端引导序列和无 5' 端引导序列的转录本的蛋白/mRNA 比值的系统差异,这表明翻译效率的可变性主要是由除了 5' 端引导序列之外的因素驱动的。我们的数据也根据另一种导致不同结论的替代模型进行了讨论,并表明无 5' 端引导序列的转录本可能确实翻译效率较低。由 引起的结核病是每年导致全球 150 万人死亡的主要公共卫生问题。在感染期间, 必须改变其基因表达模式以适应它遇到的应激条件。了解 如何调节基因表达可能为干扰细菌生存的方法提供线索。基因表达包括转录、mRNA 降解和翻译。在这里,我们使用 作为模型生物,从多个方面研究了 5'UTR 如何影响这三个方面的基因表达。我们还提供了对缺乏 5'UTR 且在分枝杆菌中异常普遍的无 5' 端引导序列 mRNA 表达的深入了解。

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