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Adaptor Molecules Epitranscriptome Reprograms Bacterial Pathogenicity

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2021 Aug 27
PMID 34445114
Citations 1
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Abstract

The strong decoration of tRNAs with post-transcriptional modifications provides an unprecedented adaptability of this class of non-coding RNAs leading to the regulation of bacterial growth and pathogenicity. Accumulating data indicate that tRNA post-transcriptional modifications possess a central role in both the formation of bacterial cell wall and the modulation of transcription and translation fidelity, but also in the expression of virulence factors. Evolutionary conserved modifications in tRNA nucleosides ensure the proper folding and stability redounding to a totally functional molecule. However, environmental factors including stress conditions can cause various alterations in tRNA modifications, disturbing the pathogen homeostasis. Post-transcriptional modifications adjacent to the anticodon stem-loop, for instance, have been tightly linked to bacterial infectivity. Currently, advances in high throughput methodologies have facilitated the identification and functional investigation of such tRNA modifications offering a broader pool of putative alternative molecular targets and therapeutic avenues against bacterial infections. Herein, we focus on tRNA epitranscriptome shaping regarding modifications with a key role in bacterial infectivity including opportunistic pathogens of the human microbiome.

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References
1.
Wright J, Keffer-Wilkes L, Dobing S, Kothe U . Pre-steady-state kinetic analysis of the three Escherichia coli pseudouridine synthases TruB, TruA, and RluA reveals uniformly slow catalysis. RNA. 2011; 17(12):2074-84. PMC: 3222121. DOI: 10.1261/rna.2905811. View

2.
Thiaville P, Iwata-Reuyl D, de Crecy-Lagard V . Diversity of the biosynthesis pathway for threonylcarbamoyladenosine (t(6)A), a universal modification of tRNA. RNA Biol. 2015; 11(12):1529-39. PMC: 4615747. DOI: 10.4161/15476286.2014.992277. View

3.
Behrens A, Rodschinka G, Nedialkova D . High-resolution quantitative profiling of tRNA abundance and modification status in eukaryotes by mim-tRNAseq. Mol Cell. 2021; 81(8):1802-1815.e7. PMC: 8062790. DOI: 10.1016/j.molcel.2021.01.028. View

4.
cavuzic M, Liu Y . Biosynthesis of Sulfur-Containing tRNA Modifications: A Comparison of Bacterial, Archaeal, and Eukaryotic Pathways. Biomolecules. 2017; 7(1). PMC: 5372739. DOI: 10.3390/biom7010027. View

5.
Li D, Shibata Y, Takeshita T, Yamashita Y . A novel gene involved in the survival of Streptococcus mutans under stress conditions. Appl Environ Microbiol. 2013; 80(1):97-103. PMC: 3910998. DOI: 10.1128/AEM.02549-13. View