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...

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Main Authors: Anahi Molla-Herman, Margarita T. Angelova, Maud Ginestet, Clément Carré, Christophe Antoniewski, Jean-René Huynh
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2020.518949/full
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author Anahi Molla-Herman
Margarita T. Angelova
Maud Ginestet
Clément Carré
Christophe Antoniewski
Jean-René Huynh
author_facet Anahi Molla-Herman
Margarita T. Angelova
Maud Ginestet
Clément Carré
Christophe Antoniewski
Jean-René Huynh
author_sort Anahi Molla-Herman
collection DOAJ
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.
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spelling doaj.art-27f5756565cf404dbd4ae5bb7d1398732022-12-22T00:19:44ZengFrontiers Media S.A.Frontiers in Genetics1664-80212020-10-011110.3389/fgene.2020.518949518949tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA MethylationAnahi Molla-Herman0Margarita T. Angelova1Maud Ginestet2Clément Carré3Christophe Antoniewski4Jean-René Huynh5Collège de France, CIRB, CNRS Inserm UMR 7241, PSL Research University, Paris, FranceTransgenerational Epigenetics & Small RNA Biology, Sorbonne Université, CNRS, Laboratoire de Biologie du Développement - Institut de Biologie Paris Seine, Paris, FranceCollège de France, CIRB, CNRS Inserm UMR 7241, PSL Research University, Paris, FranceTransgenerational Epigenetics & Small RNA Biology, Sorbonne Université, CNRS, Laboratoire de Biologie du Développement - Institut de Biologie Paris Seine, Paris, FranceARTbio Bioinformatics Analysis Facility, Sorbonne Université, CNRS, Institut de Biologie Paris Seine, Paris, FranceCollège de France, CIRB, CNRS Inserm UMR 7241, PSL Research University, Paris, FrancetRNA 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.https://www.frontiersin.org/article/10.3389/fgene.2020.518949/fullDrosophilaNm methylationRNase PtRNAtRFsoogenesis
spellingShingle Anahi Molla-Herman
Margarita T. Angelova
Maud Ginestet
Clément Carré
Christophe Antoniewski
Jean-René Huynh
tRNA Fragments Populations Analysis in Mutants Affecting tRNAs Processing and tRNA Methylation
Frontiers in Genetics
Drosophila
Nm methylation
RNase P
tRNA
tRFs
oogenesis
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 Drosophila
Nm methylation
RNase P
tRNA
tRFs
oogenesis
url https://www.frontiersin.org/article/10.3389/fgene.2020.518949/full
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