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tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation
tRNA fragments (tRFs) are a class of small non-coding RNAs (sncRNAs) derived from tRNAs. tRFs are highly abundant in many cell types including stem cells and cancer cells, and are found in all domains of life. Beyond translation control, tRFs have several functions ranging from transposon silencing...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586317/ https://www.ncbi.nlm.nih.gov/pubmed/33193603 http://dx.doi.org/10.3389/fgene.2020.518949 |
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author | Molla-Herman, Anahi Angelova, Margarita T. Ginestet, Maud Carré, Clément Antoniewski, Christophe Huynh, Jean-René |
author_facet | Molla-Herman, Anahi Angelova, Margarita T. Ginestet, Maud Carré, Clément Antoniewski, Christophe Huynh, Jean-René |
author_sort | Molla-Herman, Anahi |
collection | PubMed |
description | tRNA fragments (tRFs) are a class of small non-coding RNAs (sncRNAs) derived from tRNAs. tRFs are highly abundant in many cell types including stem cells and cancer cells, and are found in all domains of life. Beyond translation control, tRFs have several functions ranging from transposon silencing to cell proliferation control. However, the analysis of tRFs presents specific challenges and their biogenesis is not well understood. They are very heterogeneous and highly modified by numerous post-transcriptional modifications. Here we describe a bioinformatic pipeline (tRFs-Galaxy) to study tRFs populations and shed light onto tRNA fragments biogenesis in Drosophila melanogaster. Indeed, we used small RNAs Illumina sequencing datasets extracted from wild type and mutant ovaries affecting two different highly conserved steps of tRNA biogenesis: 5′pre-tRNA processing (RNase-P subunit Rpp30) and tRNA 2′-O-methylation (dTrm7_34 and dTrm7_32). Using our pipeline, we show how defects in tRNA biogenesis affect nuclear and mitochondrial tRFs populations and other small non-coding RNAs biogenesis, such as small nucleolar RNAs (snoRNAs). This tRF analysis workflow will advance the current understanding of tRFs biogenesis, which is crucial to better comprehend tRFs roles and their implication in human pathology. |
format | Online Article Text |
id | pubmed-7586317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75863172020-11-13 tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation Molla-Herman, Anahi Angelova, Margarita T. Ginestet, Maud Carré, Clément Antoniewski, Christophe Huynh, Jean-René Front Genet Genetics tRNA fragments (tRFs) are a class of small non-coding RNAs (sncRNAs) derived from tRNAs. tRFs are highly abundant in many cell types including stem cells and cancer cells, and are found in all domains of life. Beyond translation control, tRFs have several functions ranging from transposon silencing to cell proliferation control. However, the analysis of tRFs presents specific challenges and their biogenesis is not well understood. They are very heterogeneous and highly modified by numerous post-transcriptional modifications. Here we describe a bioinformatic pipeline (tRFs-Galaxy) to study tRFs populations and shed light onto tRNA fragments biogenesis in Drosophila melanogaster. Indeed, we used small RNAs Illumina sequencing datasets extracted from wild type and mutant ovaries affecting two different highly conserved steps of tRNA biogenesis: 5′pre-tRNA processing (RNase-P subunit Rpp30) and tRNA 2′-O-methylation (dTrm7_34 and dTrm7_32). Using our pipeline, we show how defects in tRNA biogenesis affect nuclear and mitochondrial tRFs populations and other small non-coding RNAs biogenesis, such as small nucleolar RNAs (snoRNAs). This tRF analysis workflow will advance the current understanding of tRFs biogenesis, which is crucial to better comprehend tRFs roles and their implication in human pathology. Frontiers Media S.A. 2020-10-09 /pmc/articles/PMC7586317/ /pubmed/33193603 http://dx.doi.org/10.3389/fgene.2020.518949 Text en Copyright © 2020 Molla-Herman, Angelova, Ginestet, Carré, Antoniewski and Huynh. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Molla-Herman, Anahi Angelova, Margarita T. Ginestet, Maud Carré, Clément Antoniewski, Christophe Huynh, Jean-René tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation |
title | tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation |
title_full | tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation |
title_fullStr | tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation |
title_full_unstemmed | tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation |
title_short | tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation |
title_sort | trna fragments populations analysis in mutants affecting trnas processing and trna methylation |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586317/ https://www.ncbi.nlm.nih.gov/pubmed/33193603 http://dx.doi.org/10.3389/fgene.2020.518949 |
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