Back to Search Start Over

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

Authors :
Chrystelle Le Danvic
Eli Sellem
Mekki Boussaha
Hélène Kiefer
Laurent Schibler
Hélène Jammes
Luc Jouneau
Sébastien Fritz
Sylvain Marthey
Jean-Philippe Perrier
Aurelie Bonnet
Andrea Rau
Biologie de la Reproduction, Environnement, Epigénétique & Développement (BREED)
École nationale vétérinaire d'Alfort (ENVA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Saclay-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Allice
Génétique Animale et Biologie Intégrative (GABI)
Université Paris-Saclay-AgroParisTech-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
ANR-14-LAB3-0008,SeQuaMol,Qualité de la semence et fertilité chez les bovins: développement de nouveaux outils moléculaires de diagnostic(2014)
Université Paris-Saclay-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-École nationale vétérinaire d'Alfort (ENVA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Source :
Epigenetics & Chromatin, Epigenetics & Chromatin, BioMed Central, 2020, 13 (1), ⟨10.1186/s13072-020-00340-0⟩, Epigenetics & Chromatin, Vol 13, Iss 1, Pp 1-28 (2020)
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

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.

Details

Language :
English
ISSN :
17568935
Database :
OpenAIRE
Journal :
Epigenetics & Chromatin, Epigenetics & Chromatin, BioMed Central, 2020, 13 (1), ⟨10.1186/s13072-020-00340-0⟩, Epigenetics & Chromatin, Vol 13, Iss 1, Pp 1-28 (2020)
Accession number :
edsair.doi.dedup.....d206f1edb19d3ee18a14c522757b8091
Full Text :
https://doi.org/10.1186/s13072-020-00340-0⟩