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Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm
BACKGROUND: During epididymal transit, spermatozoa go through several functional maturation steps, resulting from interactions with epididymal secretomes specific to each region. In particular, the sperm membrane is under constant remodeling, with sequential attachment and shedding of various molecu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146655/ https://www.ncbi.nlm.nih.gov/pubmed/34030709 http://dx.doi.org/10.1186/s13072-021-00397-5 |
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author | Sellem, Eli Marthey, Sylvain Rau, Andrea Jouneau, Luc Bonnet, Aurelie Le Danvic, Chrystelle Guyonnet, Benoît Kiefer, Hélène Jammes, Hélène Schibler, Laurent |
author_facet | Sellem, Eli Marthey, Sylvain Rau, Andrea Jouneau, Luc Bonnet, Aurelie Le Danvic, Chrystelle Guyonnet, Benoît Kiefer, Hélène Jammes, Hélène Schibler, Laurent |
author_sort | Sellem, Eli |
collection | PubMed |
description | BACKGROUND: During epididymal transit, spermatozoa go through several functional maturation steps, resulting from interactions with epididymal secretomes specific to each region. In particular, the sperm membrane is under constant remodeling, with sequential attachment and shedding of various molecules provided by the epididymal lumen fluid and epididymosomes, which also deliver sncRNA cargo to sperm. As a result, the payload of sperm sncRNAs changes during the transit from the epididymis caput to the cauda. This work was designed to study the dynamics of cattle sperm sncRNAs from spermatogenesis to final maturation. RESULTS: Comprehensive catalogues of sperm sncRNAs were obtained from testicular parenchyma, epididymal caput, corpus and cauda, as well as ejaculated semen from three Holstein bulls. The primary cattle sncRNA sperm content is markedly remodeled as sperm mature along the epididymis. Expression of piRNAs, which are abundant in testis parenchyma, decreases dramatically at epididymis. Conversely, sperm progressively acquires miRNAs, rsRNAs, and tsRNAs along epididymis, with regional specificities. For instance, miRNAs and tsRNAs are enriched in epididymis cauda and ejaculated sperm, while rsRNA expression peaks at epididymis corpus. In addition, epididymis corpus contains mainly 20 nt long piRNAs, instead of 30 nt in all other locations. Beyond the bulk differences in abundance of sncRNAs classes, K-means clustering was performed to study their spatiotemporal expression profile, highlighting differences in specific sncRNAs and providing insights into their putative biological role at each maturation stage. For instance, Gene Ontology analyses using miRNA targets highlighted enriched processes such as cell cycle regulation, response to stress and ubiquitination processes in testicular parenchyma, protein metabolism in epididymal sperm, and embryonic morphogenesis in ejaculated sperm. CONCLUSIONS: Our findings confirm that the sperm sncRNAome does not simply reflect a legacy of spermatogenesis. Instead, sperm sncRNA expression shows a remarkable level of plasticity resulting probably from the combination of multiple factors such as loss of the cytoplasmic droplet, interaction with epididymosomes, and more surprisingly, the putative in situ production and/or modification of sncRNAs by sperm. Given the suggested role of sncRNA in epigenetic trans-generational inheritance, our detailed spatiotemporal analysis may pave the way for a study of sperm sncRNAs role in embryo development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13072-021-00397-5. |
format | Online Article Text |
id | pubmed-8146655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81466552021-05-25 Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm Sellem, Eli Marthey, Sylvain Rau, Andrea Jouneau, Luc Bonnet, Aurelie Le Danvic, Chrystelle Guyonnet, Benoît Kiefer, Hélène Jammes, Hélène Schibler, Laurent Epigenetics Chromatin Research BACKGROUND: During epididymal transit, spermatozoa go through several functional maturation steps, resulting from interactions with epididymal secretomes specific to each region. In particular, the sperm membrane is under constant remodeling, with sequential attachment and shedding of various molecules provided by the epididymal lumen fluid and epididymosomes, which also deliver sncRNA cargo to sperm. As a result, the payload of sperm sncRNAs changes during the transit from the epididymis caput to the cauda. This work was designed to study the dynamics of cattle sperm sncRNAs from spermatogenesis to final maturation. RESULTS: Comprehensive catalogues of sperm sncRNAs were obtained from testicular parenchyma, epididymal caput, corpus and cauda, as well as ejaculated semen from three Holstein bulls. The primary cattle sncRNA sperm content is markedly remodeled as sperm mature along the epididymis. Expression of piRNAs, which are abundant in testis parenchyma, decreases dramatically at epididymis. Conversely, sperm progressively acquires miRNAs, rsRNAs, and tsRNAs along epididymis, with regional specificities. For instance, miRNAs and tsRNAs are enriched in epididymis cauda and ejaculated sperm, while rsRNA expression peaks at epididymis corpus. In addition, epididymis corpus contains mainly 20 nt long piRNAs, instead of 30 nt in all other locations. Beyond the bulk differences in abundance of sncRNAs classes, K-means clustering was performed to study their spatiotemporal expression profile, highlighting differences in specific sncRNAs and providing insights into their putative biological role at each maturation stage. For instance, Gene Ontology analyses using miRNA targets highlighted enriched processes such as cell cycle regulation, response to stress and ubiquitination processes in testicular parenchyma, protein metabolism in epididymal sperm, and embryonic morphogenesis in ejaculated sperm. CONCLUSIONS: Our findings confirm that the sperm sncRNAome does not simply reflect a legacy of spermatogenesis. Instead, sperm sncRNA expression shows a remarkable level of plasticity resulting probably from the combination of multiple factors such as loss of the cytoplasmic droplet, interaction with epididymosomes, and more surprisingly, the putative in situ production and/or modification of sncRNAs by sperm. Given the suggested role of sncRNA in epigenetic trans-generational inheritance, our detailed spatiotemporal analysis may pave the way for a study of sperm sncRNAs role in embryo development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13072-021-00397-5. BioMed Central 2021-05-24 /pmc/articles/PMC8146655/ /pubmed/34030709 http://dx.doi.org/10.1186/s13072-021-00397-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Le Danvic, Chrystelle Guyonnet, Benoît Kiefer, Hélène Jammes, Hélène Schibler, Laurent Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm |
title | Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm |
title_full | Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm |
title_fullStr | Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm |
title_full_unstemmed | Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm |
title_short | Dynamics of cattle sperm sncRNAs during maturation, from testis to ejaculated sperm |
title_sort | dynamics of cattle sperm sncrnas during maturation, from testis to ejaculated sperm |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146655/ https://www.ncbi.nlm.nih.gov/pubmed/34030709 http://dx.doi.org/10.1186/s13072-021-00397-5 |
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