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MicroRNA Expression during Bovine Oocyte Maturation and Fertilization

Successful fertilization and subsequent embryo development rely on complex molecular processes starting with the development of oocyte competence through maturation. MicroRNAs (miRNAs) are small non-coding RNA molecules that function as gene regulators in many biological systems, including the oocyt...

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Autores principales: Gilchrist, Graham C., Tscherner, Allison, Nalpathamkalam, Thomas, Merico, Daniele, LaMarre, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4813251/
https://www.ncbi.nlm.nih.gov/pubmed/26999121
http://dx.doi.org/10.3390/ijms17030396
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author Gilchrist, Graham C.
Tscherner, Allison
Nalpathamkalam, Thomas
Merico, Daniele
LaMarre, Jonathan
author_facet Gilchrist, Graham C.
Tscherner, Allison
Nalpathamkalam, Thomas
Merico, Daniele
LaMarre, Jonathan
author_sort Gilchrist, Graham C.
collection PubMed
description Successful fertilization and subsequent embryo development rely on complex molecular processes starting with the development of oocyte competence through maturation. MicroRNAs (miRNAs) are small non-coding RNA molecules that function as gene regulators in many biological systems, including the oocyte and embryo. In order to further explore the roles of miRNAs in oocyte maturation, we employed small RNA sequencing as a screening tool to identify and characterize miRNA populations present in pools of bovine germinal vesicle (GV) oocytes, metaphase II (MII) oocytes, and presumptive zygotes (PZ). Each stage contained a defined miRNA population, some of which showed stable expression while others showed progressive changes between stages that were subsequently confirmed by quantitative reverse transcription polymerase chain reaction (RT-PCR). Bta-miR-155, bta-miR-222, bta-miR-21, bta-let-7d, bta-let-7i, and bta-miR-190a were among the statistically significant differentially expressed miRNAs (p < 0.05). To determine whether changes in specific primary miRNA (pri-miRNA) transcripts were responsible for the observed miRNA changes, we evaluated pri-miR-155, -222 and let-7d expression. Pri-miR-155 and -222 were not detected in GV oocytes but pri-miR-155 was present in MII oocytes, indicating transcription during maturation. In contrast, levels of pri-let-7d decreased during maturation, suggesting that the observed increase in let-7d expression was likely due to processing of the primary transcript. This study demonstrates that both dynamic and stable populations of miRNAs are present in bovine oocytes and zygotes and extend previous studies supporting the importance of the small RNA landscape in the maturing bovine oocyte and early embryo.
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spelling pubmed-48132512016-04-06 MicroRNA Expression during Bovine Oocyte Maturation and Fertilization Gilchrist, Graham C. Tscherner, Allison Nalpathamkalam, Thomas Merico, Daniele LaMarre, Jonathan Int J Mol Sci Article Successful fertilization and subsequent embryo development rely on complex molecular processes starting with the development of oocyte competence through maturation. MicroRNAs (miRNAs) are small non-coding RNA molecules that function as gene regulators in many biological systems, including the oocyte and embryo. In order to further explore the roles of miRNAs in oocyte maturation, we employed small RNA sequencing as a screening tool to identify and characterize miRNA populations present in pools of bovine germinal vesicle (GV) oocytes, metaphase II (MII) oocytes, and presumptive zygotes (PZ). Each stage contained a defined miRNA population, some of which showed stable expression while others showed progressive changes between stages that were subsequently confirmed by quantitative reverse transcription polymerase chain reaction (RT-PCR). Bta-miR-155, bta-miR-222, bta-miR-21, bta-let-7d, bta-let-7i, and bta-miR-190a were among the statistically significant differentially expressed miRNAs (p < 0.05). To determine whether changes in specific primary miRNA (pri-miRNA) transcripts were responsible for the observed miRNA changes, we evaluated pri-miR-155, -222 and let-7d expression. Pri-miR-155 and -222 were not detected in GV oocytes but pri-miR-155 was present in MII oocytes, indicating transcription during maturation. In contrast, levels of pri-let-7d decreased during maturation, suggesting that the observed increase in let-7d expression was likely due to processing of the primary transcript. This study demonstrates that both dynamic and stable populations of miRNAs are present in bovine oocytes and zygotes and extend previous studies supporting the importance of the small RNA landscape in the maturing bovine oocyte and early embryo. MDPI 2016-03-18 /pmc/articles/PMC4813251/ /pubmed/26999121 http://dx.doi.org/10.3390/ijms17030396 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gilchrist, Graham C.
Tscherner, Allison
Nalpathamkalam, Thomas
Merico, Daniele
LaMarre, Jonathan
MicroRNA Expression during Bovine Oocyte Maturation and Fertilization
title MicroRNA Expression during Bovine Oocyte Maturation and Fertilization
title_full MicroRNA Expression during Bovine Oocyte Maturation and Fertilization
title_fullStr MicroRNA Expression during Bovine Oocyte Maturation and Fertilization
title_full_unstemmed MicroRNA Expression during Bovine Oocyte Maturation and Fertilization
title_short MicroRNA Expression during Bovine Oocyte Maturation and Fertilization
title_sort microrna expression during bovine oocyte maturation and fertilization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4813251/
https://www.ncbi.nlm.nih.gov/pubmed/26999121
http://dx.doi.org/10.3390/ijms17030396
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