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Research Paper|Volume 9, Issue 4|pp 1186—1201

Expression profiles and function analysis of microRNAs in postovulatory aging mouse oocytes

Tian-Yang Wang1, Jie Zhang1, Jiang Zhu1, Hua-Yu Lian1, Hong-Jie Yuan1, Min Gao1, Ming-Jiu Luo1, Jing-He Tan1
  • 1College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City 271018, P. R. China

* * Equal contribution

Received: March 3, 2017Accepted: March 28, 2017Published: April 8, 2017

Copyright: © 2017 Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

In this study, microRNA (miRNA) profiles in postovulatory aging mouse oocytes were analyzed by microarray screening and RT-qPCR. Hierarchical cluster analysis on the microarray data and KEGG pathway enrichment analysis on the mRNAs targeted by differentially expressed (DE) miRNAs between two adjacent egg-ages suggest that while only a mild alteration in miRNA expression occurred from 13 to 18 h, a great change took place from 18 to 24 h post hCG injection. Theoretical exploration on functions of the predicted target genes suggest that KEGG pathways enriched by 13-18 h DE miRNAs are correlated with early events of oocyte aging while pathways most enriched by 18-24 h or 24-30 h DE miRNAs are correlated with the late symptoms of aged oocytes. Experimental verification on functions of the key proteins predicted by the KEGG analysis and injection of miR-98 mimics or inhibitors further confirmed that miRNAs played stimulatory/inhibitory roles in postovulatory oocyte aging. In conclusion, marked changes in miRNA expression are associated with significant alterations in function and morphology of postovulatory aging oocytes.