Communication Analysis of tRNA-Derived Fragment Uptake and Signalling in Neurons

Transfer RNAs (tRNAs) are a family of non-coding ribonucleic acids (RNAs) that are involved in protein translation. Cleavage of tRNA through stress-induced ribonucleases results in the production of short tRNA-derived small RNAs (tsRNAs), such as tRNA-derived fragments (tRFs). Recent studies have identified three tRFs-5'AlaTGC, 5'GluCTC, and 5'GlyGCC-to be released from neurons and significantly elevated in epilepsy patients. Extracellular 5 'tRFs are taken up by neurons and act in paracrine to inhibit protein translation. We hereby explored a molecular communications (MC) approach to investigate biological effects of tRFs in neurons. Temporal dynamics and biophysical interactions of tRFs across the neuronal microdomain were expressed mathematically, and system communications performances were evaluated. The devised MC tool may aid in the interpretation of tRFs and their uptake and activities in neurons relevant to their potential as seizure biomarkers and neurotherapeutics.

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Published
2025-02-27
DOI
https://doi.org/10.1109/icbcb64873.2025.11197993
Primary Topic
RNA modifications and cancer
Type
article
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article

Communication Analysis of tRNA-Derived Fragment Uptake and Signalling in Neurons

Rachel L. Stewart, Steven G. Fagan, Daniel P. Martins, Jochen H.M. Prehn et al.
RNA modifications and cancer
article

Communication Analysis of tRNA-Derived Fragment Uptake and Signalling in Neurons

Rachel L. Stewart, Steven G. Fagan, Daniel P. Martins, Jochen H.M. Prehn, Deirdre Kilbane, Kurt J. A. Pumares
article en

Abstract

Transfer RNAs (tRNAs) are a family of non-coding ribonucleic acids (RNAs) that are involved in protein translation. Cleavage of tRNA through stress-induced ribonucleases results in the production of short tRNA-derived small RNAs (tsRNAs), such as tRNA-derived fragments (tRFs). Recent studies have identified three tRFs-5'AlaTGC, 5'GluCTC, and 5'GlyGCC-to be released from neurons and significantly elevated in epilepsy patients. Extracellular 5 'tRFs are taken up by neurons and act in paracrine to inhibit protein translation. We hereby explored a molecular communications (MC) approach to investigate biological effects of tRFs in neurons. Temporal dynamics and biophysical interactions of tRFs across the neuronal microdomain were expressed mathematically, and system communications performances were evaluated. The devised MC tool may aid in the interpretation of tRFs and their uptake and activities in neurons relevant to their potential as seizure biomarkers and neurotherapeutics.

University of Essex (GB), Royal College of Surgeons in Ireland (IE), Waterford Institute of Technology (IE)
Openalex Percentile: Top 74%
RNA modifications and cancer
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