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Identification of miRNAs during mouse postnatal ovarian development and superovulation

BACKGROUND: MicroRNAs are small noncoding RNAs that play critical roles in regulation of gene expression in wide array of tissues including the ovary through sequence complementarity at post-transcriptional level. Tight regulation of multitude of genes involved in ovarian development and folliculoge...

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Autores principales: Khan, Hamid Ali, Zhao, Yi, Wang, Li, Li, Qian, Du, Yu-Ai, Dan, Yi, Huo, Li-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499447/
https://www.ncbi.nlm.nih.gov/pubmed/26152307
http://dx.doi.org/10.1186/s13048-015-0170-2
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author Khan, Hamid Ali
Zhao, Yi
Wang, Li
Li, Qian
Du, Yu-Ai
Dan, Yi
Huo, Li-Jun
author_facet Khan, Hamid Ali
Zhao, Yi
Wang, Li
Li, Qian
Du, Yu-Ai
Dan, Yi
Huo, Li-Jun
author_sort Khan, Hamid Ali
collection PubMed
description BACKGROUND: MicroRNAs are small noncoding RNAs that play critical roles in regulation of gene expression in wide array of tissues including the ovary through sequence complementarity at post-transcriptional level. Tight regulation of multitude of genes involved in ovarian development and folliculogenesis could be regulated at transcription level by these miRNAs. Therefore, tissue specific miRNAs identification is considered a key step towards understanding the role of miRNAs in biological processes. METHODS: To investigate the role of microRNAs during ovarian development and folliculogenesis we sequenced eight different libraries using Illumina deep sequencing technology. Different developmental stages were selected to explore miRNAs expression pattern at different stages of gonadal maturation with/without treatment of PMSG/hCG for superovulation. RESULTS: From massive sequencing reads, clean reads of 16–26 bp were selected for further analysis of differential expression analysis and novel microRNA annotation. Expression analysis of all miRNAs at different developmental stages showed that some miRNAs were present ubiquitously while others were differentially expressed at different stages. Among differentially expressed miRNAs we reported 61 miRNAs with a fold change of more than 2 at different developmental stages among all libraries. Among the up-regulated miRNAs, mmu-mir-1298 had the highest fold change with 4.025 while mmu-mir-150 was down-regulated more than 3 fold. Furthermore, we found 2659 target genes for 20 differentially expressed microRNAs using seven different target predictions programs (DIANA-mT, miRanda, miRDB, miRWalk, RNAhybrid, PICTAR5, TargetScan). Analysis of the predicted targets showed certain ovary specific genes targeted by single or multiple microRNAs. Furthermore, pathway annotation and Gene ontology showed involvement of these microRNAs in basic cellular process. CONCLUSIONS: These results suggest the presence of different miRNAs at different stages of ovarian development and superovulation. Potential role of these microRNAs was elucidated using bioinformatics tools in regulation of different pathways, biological functions and cellular components underlying ovarian development and superovulation. These results provide a framework for extended analysis of miRNAs and their roles during ovarian development and superovulation. Furthermore, this study provides a base for characterization of individual miRNAs to discover their role in ovarian development and female fertility. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13048-015-0170-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-44994472015-07-13 Identification of miRNAs during mouse postnatal ovarian development and superovulation Khan, Hamid Ali Zhao, Yi Wang, Li Li, Qian Du, Yu-Ai Dan, Yi Huo, Li-Jun J Ovarian Res Research BACKGROUND: MicroRNAs are small noncoding RNAs that play critical roles in regulation of gene expression in wide array of tissues including the ovary through sequence complementarity at post-transcriptional level. Tight regulation of multitude of genes involved in ovarian development and folliculogenesis could be regulated at transcription level by these miRNAs. Therefore, tissue specific miRNAs identification is considered a key step towards understanding the role of miRNAs in biological processes. METHODS: To investigate the role of microRNAs during ovarian development and folliculogenesis we sequenced eight different libraries using Illumina deep sequencing technology. Different developmental stages were selected to explore miRNAs expression pattern at different stages of gonadal maturation with/without treatment of PMSG/hCG for superovulation. RESULTS: From massive sequencing reads, clean reads of 16–26 bp were selected for further analysis of differential expression analysis and novel microRNA annotation. Expression analysis of all miRNAs at different developmental stages showed that some miRNAs were present ubiquitously while others were differentially expressed at different stages. Among differentially expressed miRNAs we reported 61 miRNAs with a fold change of more than 2 at different developmental stages among all libraries. Among the up-regulated miRNAs, mmu-mir-1298 had the highest fold change with 4.025 while mmu-mir-150 was down-regulated more than 3 fold. Furthermore, we found 2659 target genes for 20 differentially expressed microRNAs using seven different target predictions programs (DIANA-mT, miRanda, miRDB, miRWalk, RNAhybrid, PICTAR5, TargetScan). Analysis of the predicted targets showed certain ovary specific genes targeted by single or multiple microRNAs. Furthermore, pathway annotation and Gene ontology showed involvement of these microRNAs in basic cellular process. CONCLUSIONS: These results suggest the presence of different miRNAs at different stages of ovarian development and superovulation. Potential role of these microRNAs was elucidated using bioinformatics tools in regulation of different pathways, biological functions and cellular components underlying ovarian development and superovulation. These results provide a framework for extended analysis of miRNAs and their roles during ovarian development and superovulation. Furthermore, this study provides a base for characterization of individual miRNAs to discover their role in ovarian development and female fertility. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13048-015-0170-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-08 /pmc/articles/PMC4499447/ /pubmed/26152307 http://dx.doi.org/10.1186/s13048-015-0170-2 Text en © Khan et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Khan, Hamid Ali
Zhao, Yi
Wang, Li
Li, Qian
Du, Yu-Ai
Dan, Yi
Huo, Li-Jun
Identification of miRNAs during mouse postnatal ovarian development and superovulation
title Identification of miRNAs during mouse postnatal ovarian development and superovulation
title_full Identification of miRNAs during mouse postnatal ovarian development and superovulation
title_fullStr Identification of miRNAs during mouse postnatal ovarian development and superovulation
title_full_unstemmed Identification of miRNAs during mouse postnatal ovarian development and superovulation
title_short Identification of miRNAs during mouse postnatal ovarian development and superovulation
title_sort identification of mirnas during mouse postnatal ovarian development and superovulation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499447/
https://www.ncbi.nlm.nih.gov/pubmed/26152307
http://dx.doi.org/10.1186/s13048-015-0170-2
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