The maternal-to-zygotic transition in bovine in vitro-fertilized embryos is associated with marked changes in small non-coding RNAs†.


Journal

Biology of reproduction
ISSN: 1529-7268
Titre abrégé: Biol Reprod
Pays: United States
ID NLM: 0207224

Informations de publication

Date de publication:
01 02 2019
Historique:
received: 18 05 2018
revised: 25 07 2018
accepted: 23 08 2018
pubmed: 31 8 2018
medline: 31 3 2020
entrez: 31 8 2018
Statut: ppublish

Résumé

In mammals, small non-coding RNAs (sncRNAs) have been reported to be important during early embryo development. However, a comprehensive assessment of the inventory of sncRNAs during the maternal-to-zygotic transition (MZT) has not been performed in an animal model that better represents the sncRNA biogenesis pathway in human oocytes and embryos. The objective of this study was to examine dynamic changes in expression of sncRNAs during the MZT in bovine embryos produced by in vitro fertilization (IVF), which occurs at the 8-cell stage. An unbiased, discovery-based approach was employed using small RNAseq to profile sncRNAs in bovine oocytes, 8-cell stage embryos and blastocyst stage embryos followed by network and ontology analyses to explore the functional relevance of differentially expressed micro-RNAS (miRNAs). The relative abundance of miRNAs was markedly higher in 8-cell stage embryos compared to oocytes or blastocyst stage embryos. This shift in miRNA population was largely associated with upregulation of miRNAs predicted to target genes involved in the biological processes of cell development, cell division, Wnt signaling, and pluripotency, among others. Distinct populations of piwi-interacting-like RNAs (pilRNAs) were identified in bovine oocytes and blastocyst stage embryos, though pilRNAs were nearly absent in 8-cell stage embryos. Also, small nucleolar RNAs were highly expressed in 8-cell stage embryos. Overall, these data reveal a strong dynamic shift in the relative abundance of sncRNAs associated with the MZT in bovine oocytes and embryos, suggesting that these molecules may play important roles in the shift from maternal to zygotic control of gene expression.

Identifiants

pubmed: 30165428
pii: 5079635
doi: 10.1093/biolre/ioy190
doi:

Substances chimiques

MicroRNAs 0
RNA, Small Untranslated 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

331-350

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press on behalf of Society for the Study of Reproduction.

Auteurs

Jocelyn M Cuthbert (JM)

Department of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, Utah, USA.

Stewart J Russell (SJ)

CReATe Fertility Centre, Toronto, Ontario, Canada.

Kenneth L White (KL)

Department of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, Utah, USA.
School of Veterinary Medicine, Utah State University, Logan, Utah, USA.

Abby D Benninghoff (AD)

Department of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, Utah, USA.
School of Veterinary Medicine, Utah State University, Logan, Utah, USA.

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Classifications MeSH