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A tRNA-derived fragment present in E. coli OMVs regulates host cell gene expression and proliferation. | LitMetric

A tRNA-derived fragment present in E. coli OMVs regulates host cell gene expression and proliferation.

PLoS Pathog

CHU de Québec-Université Laval Research Center/CHUL Pavilion, Department of Microbiology, Infectious Diseases and Immunology, Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada.

Published: September 2022

AI Article Synopsis

  • Scientists have discovered a lot more about small RNAs (sRNAs) in bacteria thanks to a method called RNA-sequencing.
  • These tiny RNAs can be found in outer membrane vesicles (OMVs), which could affect how bacteria interact with their hosts, like humans, but not many studies have looked into this.
  • One specific small RNA called Ile-tRF-5X was found in E. coli and changes with stress, and it can move to human cells where it helps express a certain protein.

Article Abstract

RNA-sequencing has led to a spectacular increase in the repertoire of bacterial sRNAs and improved our understanding of their biological functions. Bacterial sRNAs have also been found in outer membrane vesicles (OMVs), raising questions about their potential involvement in bacteria-host relationship, but few studies have documented this issue. Recent RNA-Sequencing analyses of bacterial RNA unveiled the existence of abundant very small RNAs (vsRNAs) shorter than 16 nt. These especially include tRNA fragments (tRFs) that are selectively loaded in OMVs and are predicted to target host mRNAs. Here, in Escherichia coli (E. coli), we report the existence of an abundant vsRNA, Ile-tRF-5X, which is selectively modulated by environmental stress, while remaining unaffected by inhibition of transcription or translation. Ile-tRF-5X is released through OMVs and can be transferred to human HCT116 cells, where it promoted MAP3K4 expression. Our findings provide a novel perspective and paradigm on the existing symbiosis between bacteria and human cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9514646PMC
http://dx.doi.org/10.1371/journal.ppat.1010827DOI Listing

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