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Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos
Embryos utilize oocyte-donated RNAs until they become capable of producing RNAs through embryonic genome activation (EGA). The sperm’s influence over pre-EGA RNA content of embryos remains unknown. Recent studies have revealed that sperm donate non-genomic components upon fertilization. Thus, sperm...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937301/ https://www.ncbi.nlm.nih.gov/pubmed/31889064 http://dx.doi.org/10.1038/s41598-019-55868-3 |
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author | Gross, Nicole Strillacci, Maria Giuseppina Peñagaricano, Francisco Khatib, Hasan |
author_facet | Gross, Nicole Strillacci, Maria Giuseppina Peñagaricano, Francisco Khatib, Hasan |
author_sort | Gross, Nicole |
collection | PubMed |
description | Embryos utilize oocyte-donated RNAs until they become capable of producing RNAs through embryonic genome activation (EGA). The sperm’s influence over pre-EGA RNA content of embryos remains unknown. Recent studies have revealed that sperm donate non-genomic components upon fertilization. Thus, sperm may also contribute to RNA presence in pre-EGA embryos. The first objective of this study was to investigate whether male fertility status is associated with the RNAs present in the bovine embryo prior to EGA. A total of 65 RNAs were found to be differentially expressed between 2–4 cell bovine embryos derived from high and low fertility sires. Expression patterns were confirmed for protein phosphatase 1 regulatory subunit 36 (PPP1R36) and ataxin 2 like (ATXN2L) in three new biological replicates. The knockdown of ATXN2L led to a 22.9% increase in blastocyst development. The second objective of this study was to characterize the parental origin of RNAs present in pre-EGA embryos. Results revealed 472 sperm-derived RNAs, 2575 oocyte-derived RNAs, 2675 RNAs derived from both sperm and oocytes, and 663 embryo-exclusive RNAs. This study uncovers an association of male fertility with developmentally impactful RNAs in 2–4 cell embryos. This study also provides an initial characterization of paternally-contributed RNAs to pre-EGA embryos. Furthermore, a subset of 2–4 cell embryo-specific RNAs was identified. |
format | Online Article Text |
id | pubmed-6937301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69373012020-01-06 Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos Gross, Nicole Strillacci, Maria Giuseppina Peñagaricano, Francisco Khatib, Hasan Sci Rep Article Embryos utilize oocyte-donated RNAs until they become capable of producing RNAs through embryonic genome activation (EGA). The sperm’s influence over pre-EGA RNA content of embryos remains unknown. Recent studies have revealed that sperm donate non-genomic components upon fertilization. Thus, sperm may also contribute to RNA presence in pre-EGA embryos. The first objective of this study was to investigate whether male fertility status is associated with the RNAs present in the bovine embryo prior to EGA. A total of 65 RNAs were found to be differentially expressed between 2–4 cell bovine embryos derived from high and low fertility sires. Expression patterns were confirmed for protein phosphatase 1 regulatory subunit 36 (PPP1R36) and ataxin 2 like (ATXN2L) in three new biological replicates. The knockdown of ATXN2L led to a 22.9% increase in blastocyst development. The second objective of this study was to characterize the parental origin of RNAs present in pre-EGA embryos. Results revealed 472 sperm-derived RNAs, 2575 oocyte-derived RNAs, 2675 RNAs derived from both sperm and oocytes, and 663 embryo-exclusive RNAs. This study uncovers an association of male fertility with developmentally impactful RNAs in 2–4 cell embryos. This study also provides an initial characterization of paternally-contributed RNAs to pre-EGA embryos. Furthermore, a subset of 2–4 cell embryo-specific RNAs was identified. Nature Publishing Group UK 2019-12-30 /pmc/articles/PMC6937301/ /pubmed/31889064 http://dx.doi.org/10.1038/s41598-019-55868-3 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gross, Nicole Strillacci, Maria Giuseppina Peñagaricano, Francisco Khatib, Hasan Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos |
title | Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos |
title_full | Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos |
title_fullStr | Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos |
title_full_unstemmed | Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos |
title_short | Characterization and functional roles of paternal RNAs in 2–4 cell bovine embryos |
title_sort | characterization and functional roles of paternal rnas in 2–4 cell bovine embryos |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937301/ https://www.ncbi.nlm.nih.gov/pubmed/31889064 http://dx.doi.org/10.1038/s41598-019-55868-3 |
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