The ribosome-associated quality control pathway supports survival in the absence of non-stop ribosome rescue factors.

IF 5.1 1区 生物学 Q1 MICROBIOLOGY mBio Pub Date : 2024-11-13 DOI:10.1128/mbio.02322-24
Katrina Callan, Cassidy R Prince, Heather A Feaga
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Abstract

In bacteria, if a ribosome translates an mRNA lacking a stop codon it becomes stalled at the 3' end of the message. These ribosomes must be rescued by trans-translation or the alternative rescue factors (ArfA or ArfB). However, mounting evidence suggests that the ribosome quality control (RQC) pathway may also rescue non-stop ribosomes. Here, we surveyed the conservation of ribosome rescue pathways in >15,000 bacterial genomes. We found that trans-translation is conserved in >97% of bacterial genomes, while the other rescue pathways are restricted to particular phyla. We did not detect the gene encoding RqcH, the major mediator of RQC, in Proteobacteria (Pseudomonadota). In all Proteobacteria investigated to date, trans-translation is essential in the absence of the Arf proteins. Therefore, we tested whether expression of RQC components from Bacillus subtilis could rescue viability in the absence of trans-translation and ArfA in Escherichia coli. We found that the RQC pathway indeed functions in E. coli and rescues the well-documented synthetic lethal phenotype of ∆ssrAarfA. Moreover, we show that the RQC pathway in B. subtilis is essential in the absence of trans-translation and ArfA, further supporting a role for the RQC pathway in the rescue of non-stop ribosomes. Finally, we report a strong co-occurrence between RqcH and the ribosome splitting factor MutS2, but present experimental evidence that there are likely additional ribosome splitting factors beyond MutS2 in B. subtilis. Altogether, our work supports a role for RQC in non-stop ribosome rescue and provides a broad survey of ribosome rescue pathways in diverse bacteria.

Importance: In bacteria, it is estimated that 2%-4% of all translation reactions terminate with the ribosome stalled on a damaged mRNA lacking a stop codon. Mechanisms that rescue these ribosomes are essential for viability. We determined the functional overlap between the ribosome quality control pathway and the classical non-stop rescue systems [alternative rescue factor (ArfA) and trans-translation] in a representative Firmicute and Proteobacterium, phyla that are evolutionarily distinct. Furthermore, we used a bioinformatics approach to examine the conservation and overlap of various ribosome rescue systems in >15,000 species throughout the bacterial domain. These results provide key insights into ribosome rescue in diverse phyla.

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核糖体相关质量控制途径可在缺乏不间断核糖体拯救因子的情况下支持存活。
在细菌中,如果核糖体翻译缺少终止密码子的 mRNA,就会停滞在信息的 3' 端。这些核糖体必须通过转译或替代拯救因子(ArfA 或 ArfB)来拯救。然而,越来越多的证据表明,核糖体质量控制(RQC)途径也可能挽救不停止的核糖体。在这里,我们调查了超过 15,000 个细菌基因组中核糖体拯救途径的保存情况。我们发现,转译在超过 97% 的细菌基因组中是保守的,而其他拯救途径则仅限于特定的门类。我们在变形菌(假单胞菌)中没有检测到编码 RQC 主要介质 RqcH 的基因。在迄今为止调查过的所有变形菌中,在没有 Arf 蛋白的情况下,转译是必不可少的。因此,我们测试了枯草芽孢杆菌 RQC 成分的表达能否在大肠杆菌缺乏转译和 ArfA 的情况下挽救其生命力。我们发现,RQC 通路在大肠杆菌中确实起作用,并能挽救已被充分证明的 ∆ssrA∆arfA 合成致死表型。此外,我们还发现在缺乏转译和 ArfA 的情况下,枯草芽孢杆菌中的 RQC 通路也是必不可少的,这进一步支持了 RQC 通路在挽救非停止核糖体中的作用。最后,我们报告了 RqcH 与核糖体分裂因子 MutS2 之间的密切共存关系,但实验证据表明,除了 MutS2 之外,枯草杆菌中可能还有其他核糖体分裂因子。总之,我们的工作支持了 RQC 在不停顿核糖体拯救中的作用,并提供了对不同细菌中核糖体拯救途径的广泛调查:在细菌中,据估计有 2%-4% 的翻译反应因核糖体停滞在缺乏终止密码子的受损 mRNA 上而终止。挽救这些核糖体的机制对于生存至关重要。我们确定了核糖体质量控制途径与经典不停顿拯救系统 [替代拯救因子(ArfA)和转译] 在具有代表性的固氮菌和变形菌(进化过程中截然不同的门类)中的功能重叠。此外,我们还利用生物信息学方法,研究了整个细菌领域超过 15,000 个物种中各种核糖体救援系统的保护和重叠情况。这些结果为我们深入了解不同门类的核糖体拯救系统提供了重要依据。
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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
期刊最新文献
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