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A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds

BACKGROUND: Mature sperm carry thousands of RNAs, including mRNAs, lncRNAs, tRNAs, rRNAs and sncRNAs, though their functional significance is still a matter of debate. Growing evidence suggests that sperm RNAs, especially sncRNAs, are selectively retained during spermiogenesis or specifically transf...

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Autores principales: Sellem, Eli, Marthey, Sylvain, Rau, Andrea, Jouneau, Luc, Bonnet, Aurelie, Perrier, Jean-Philippe, Fritz, Sébastien, Le Danvic, Chrystelle, Boussaha, Mekki, Kiefer, Hélène, Jammes, Hélène, Schibler, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106649/
https://www.ncbi.nlm.nih.gov/pubmed/32228651
http://dx.doi.org/10.1186/s13072-020-00340-0
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author Sellem, Eli
Marthey, Sylvain
Rau, Andrea
Jouneau, Luc
Bonnet, Aurelie
Perrier, Jean-Philippe
Fritz, Sébastien
Le Danvic, Chrystelle
Boussaha, Mekki
Kiefer, Hélène
Jammes, Hélène
Schibler, Laurent
author_facet Sellem, Eli
Marthey, Sylvain
Rau, Andrea
Jouneau, Luc
Bonnet, Aurelie
Perrier, Jean-Philippe
Fritz, Sébastien
Le Danvic, Chrystelle
Boussaha, Mekki
Kiefer, Hélène
Jammes, Hélène
Schibler, Laurent
author_sort Sellem, Eli
collection PubMed
description BACKGROUND: Mature sperm carry thousands of RNAs, including mRNAs, lncRNAs, tRNAs, rRNAs and sncRNAs, though their functional significance is still a matter of debate. Growing evidence suggests that sperm RNAs, especially sncRNAs, are selectively retained during spermiogenesis or specifically transferred during epididymis maturation, and are thus delivered to the oocyte at fertilization, providing resources for embryo development. However , a deep characterization of the sncRNA content of bull sperm and its expression profile across breeds is currently lacking. To fill this gap, we optimized a guanidinium–Trizol total RNA extraction protocol to prepare high-quality RNA from frozen bull sperm collected from 40 representative bulls from six breeds. Deep sequencing was performed (40 M single 50-bp reads per sample) to establish a comprehensive repertoire of cattle sperm sncRNA. RESULTS: Our study showed that it comprises mostly piRNAs (26%), rRNA fragments (25%), miRNAs (20%) and tRNA fragments (tsRNA, 14%). We identified 5p-halves as the predominant tsRNA subgroup in bull sperm, originating mostly from Gly and Glu isoacceptors. Our study also increased by ~ 50% the sperm repertoire of known miRNAs and identified 2022 predicted miRNAs. About 20% of sperm miRNAs were located within genomic clusters, expanding the list of known polycistronic pri-miRNA clusters and defining several networks of co-expressed miRNAs. Strikingly, our study highlighted the great diversity of isomiRs, resulting mainly from deletions and non-templated additions (A and U) at the 3p end. Substitutions within miRNA sequence accounted for 40% of isomiRs, with G>A, U>C and C>U substitutions being the most frequent variations. In addition, many sncRNAs were found to be differentially expressed across breeds. CONCLUSIONS: Our study provides a comprehensive overview of cattle sperm sncRNA, and these findings will pave the way for future work on the role of sncRNAs in embryo development and their relevance as biomarkers of semen fertility.
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spelling pubmed-71066492020-04-01 A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds Sellem, Eli Marthey, Sylvain Rau, Andrea Jouneau, Luc Bonnet, Aurelie Perrier, Jean-Philippe Fritz, Sébastien Le Danvic, Chrystelle Boussaha, Mekki Kiefer, Hélène Jammes, Hélène Schibler, Laurent Epigenetics Chromatin Research BACKGROUND: Mature sperm carry thousands of RNAs, including mRNAs, lncRNAs, tRNAs, rRNAs and sncRNAs, though their functional significance is still a matter of debate. Growing evidence suggests that sperm RNAs, especially sncRNAs, are selectively retained during spermiogenesis or specifically transferred during epididymis maturation, and are thus delivered to the oocyte at fertilization, providing resources for embryo development. However , a deep characterization of the sncRNA content of bull sperm and its expression profile across breeds is currently lacking. To fill this gap, we optimized a guanidinium–Trizol total RNA extraction protocol to prepare high-quality RNA from frozen bull sperm collected from 40 representative bulls from six breeds. Deep sequencing was performed (40 M single 50-bp reads per sample) to establish a comprehensive repertoire of cattle sperm sncRNA. RESULTS: Our study showed that it comprises mostly piRNAs (26%), rRNA fragments (25%), miRNAs (20%) and tRNA fragments (tsRNA, 14%). We identified 5p-halves as the predominant tsRNA subgroup in bull sperm, originating mostly from Gly and Glu isoacceptors. Our study also increased by ~ 50% the sperm repertoire of known miRNAs and identified 2022 predicted miRNAs. About 20% of sperm miRNAs were located within genomic clusters, expanding the list of known polycistronic pri-miRNA clusters and defining several networks of co-expressed miRNAs. Strikingly, our study highlighted the great diversity of isomiRs, resulting mainly from deletions and non-templated additions (A and U) at the 3p end. Substitutions within miRNA sequence accounted for 40% of isomiRs, with G>A, U>C and C>U substitutions being the most frequent variations. In addition, many sncRNAs were found to be differentially expressed across breeds. CONCLUSIONS: Our study provides a comprehensive overview of cattle sperm sncRNA, and these findings will pave the way for future work on the role of sncRNAs in embryo development and their relevance as biomarkers of semen fertility. BioMed Central 2020-03-30 /pmc/articles/PMC7106649/ /pubmed/32228651 http://dx.doi.org/10.1186/s13072-020-00340-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sellem, Eli
Marthey, Sylvain
Rau, Andrea
Jouneau, Luc
Bonnet, Aurelie
Perrier, Jean-Philippe
Fritz, Sébastien
Le Danvic, Chrystelle
Boussaha, Mekki
Kiefer, Hélène
Jammes, Hélène
Schibler, Laurent
A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds
title A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds
title_full A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds
title_fullStr A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds
title_full_unstemmed A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds
title_short A comprehensive overview of bull sperm-borne small non-coding RNAs and their diversity across breeds
title_sort comprehensive overview of bull sperm-borne small non-coding rnas and their diversity across breeds
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106649/
https://www.ncbi.nlm.nih.gov/pubmed/32228651
http://dx.doi.org/10.1186/s13072-020-00340-0
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