Lampi Mirka, Gregorova Pavlina, Qasim M Suleman, Ahlblad Niklas C V, Sarin L Peter
RNAcious Laboratory, Molecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, FI-00014 Helsinki, Finland.
Doctoral Programme in Integrative Life Science, University of Helsinki, FI-00014 Helsinki, Finland.
Microorganisms. 2023 Jan 31;11(2):355. doi: 10.3390/microorganisms11020355.
Viruses are obligate intracellular parasites that, throughout evolution, have adapted numerous strategies to control the translation machinery, including the modulation of post-transcriptional modifications (PTMs) on transfer RNA (tRNA). PTMs are critical translation regulators used to further host immune responses as well as the expression of viral proteins. Yet, we lack critical insight into the temporal dynamics of infection-induced changes to the tRNA modification landscape (i.e., 'modificome'). In this study, we provide the first comprehensive quantitative characterization of the tRNA modificome in the marine bacterium during Shewanella phage 1/4 infection. Specifically, we show that PTMs can be grouped into distinct categories based on modification level changes at various infection stages. Furthermore, we observe a preference for the UAC codon in viral transcripts expressed at the late stage of infection, which coincides with an increase in queuosine modification. Queuosine appears exclusively on tRNAs with GUN anticodons, suggesting a correlation between phage codon usage and PTM modification. Importantly, this work provides the basis for further studies into RNA-based regulatory mechanisms employed by bacteriophages to control the prokaryotic translation machinery.
病毒是专性细胞内寄生虫,在整个进化过程中,它们采用了多种策略来控制翻译机制,包括调节转运RNA(tRNA)上的转录后修饰(PTM)。PTM是关键的翻译调节因子,用于进一步调节宿主免疫反应以及病毒蛋白的表达。然而,我们对感染诱导的tRNA修饰图谱(即“修饰组”)变化的时间动态缺乏关键认识。在本研究中,我们首次全面定量表征了海洋细菌在感染希瓦氏菌噬菌体1/4期间的tRNA修饰组。具体而言,我们表明PTM可根据不同感染阶段的修饰水平变化分为不同类别。此外,我们观察到在感染后期表达的病毒转录本中对UAC密码子有偏好,这与queuosine修饰的增加相吻合。Queuosine仅出现在带有GUN反密码子的tRNA上,表明噬菌体密码子使用与PTM修饰之间存在关联。重要的是,这项工作为进一步研究噬菌体用于控制原核翻译机制的基于RNA的调控机制提供了基础。