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Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs

BACKGROUND: MicroRNAs (miRNAs) exist pervasively across viruses, plants and animals and play important roles in the post-transcriptional regulation of genes. In the common carp, miRNA targets have not been investigated. In model species, single-nucleotide polymorphisms (SNPs) have been reported to i...

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Autores principales: Zhu, Ya-Ping, Xue, Wei, Wang, Jin-Tu, Wan, Yu-Mei, Wang, Shao-Lin, Xu, Peng, Zhang, Yan, Li, Jiong-Tang, Sun, Xiao-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478155/
https://www.ncbi.nlm.nih.gov/pubmed/22908890
http://dx.doi.org/10.1186/1471-2164-13-413
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author Zhu, Ya-Ping
Xue, Wei
Wang, Jin-Tu
Wan, Yu-Mei
Wang, Shao-Lin
Xu, Peng
Zhang, Yan
Li, Jiong-Tang
Sun, Xiao-Wen
author_facet Zhu, Ya-Ping
Xue, Wei
Wang, Jin-Tu
Wan, Yu-Mei
Wang, Shao-Lin
Xu, Peng
Zhang, Yan
Li, Jiong-Tang
Sun, Xiao-Wen
author_sort Zhu, Ya-Ping
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) exist pervasively across viruses, plants and animals and play important roles in the post-transcriptional regulation of genes. In the common carp, miRNA targets have not been investigated. In model species, single-nucleotide polymorphisms (SNPs) have been reported to impair or enhance miRNA regulation as well as to alter miRNA biogenesis. SNPs are often associated with diseases or traits. To date, no studies into the effects of SNPs on miRNA biogenesis and regulation in the common carp have been reported. RESULTS: Using homology-based prediction combined with small RNA sequencing, we have identified 113 common carp mature miRNAs, including 92 conserved miRNAs and 21 common carp specific miRNAs. The conserved miRNAs had significantly higher expression levels than the specific miRNAs. The miRNAs were clustered into three phylogenetic groups. Totally 394 potential miRNA binding sites in 206 target mRNAs were predicted for 83 miRNAs. We identified 13 SNPs in the miRNA precursors. Among them, nine SNPs had the potential to either increase or decrease the energy of the predicted secondary structures of the precursors. Further, two SNPs in the 3’ untranslated regions of target genes were predicted to either disturb or create miRNA-target interactions. CONCLUSIONS: The common carp miRNAs and their target genes reported here will help further our understanding of the role of miRNAs in gene regulation. The analysis of the miRNA-related SNPs and their effects provided insights into the effects of SNPs on miRNA biogenesis and function. The resource data generated in this study will help advance the study of miRNA function and phenotype-associated miRNA identification.
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spelling pubmed-34781552012-10-23 Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs Zhu, Ya-Ping Xue, Wei Wang, Jin-Tu Wan, Yu-Mei Wang, Shao-Lin Xu, Peng Zhang, Yan Li, Jiong-Tang Sun, Xiao-Wen BMC Genomics Research Article BACKGROUND: MicroRNAs (miRNAs) exist pervasively across viruses, plants and animals and play important roles in the post-transcriptional regulation of genes. In the common carp, miRNA targets have not been investigated. In model species, single-nucleotide polymorphisms (SNPs) have been reported to impair or enhance miRNA regulation as well as to alter miRNA biogenesis. SNPs are often associated with diseases or traits. To date, no studies into the effects of SNPs on miRNA biogenesis and regulation in the common carp have been reported. RESULTS: Using homology-based prediction combined with small RNA sequencing, we have identified 113 common carp mature miRNAs, including 92 conserved miRNAs and 21 common carp specific miRNAs. The conserved miRNAs had significantly higher expression levels than the specific miRNAs. The miRNAs were clustered into three phylogenetic groups. Totally 394 potential miRNA binding sites in 206 target mRNAs were predicted for 83 miRNAs. We identified 13 SNPs in the miRNA precursors. Among them, nine SNPs had the potential to either increase or decrease the energy of the predicted secondary structures of the precursors. Further, two SNPs in the 3’ untranslated regions of target genes were predicted to either disturb or create miRNA-target interactions. CONCLUSIONS: The common carp miRNAs and their target genes reported here will help further our understanding of the role of miRNAs in gene regulation. The analysis of the miRNA-related SNPs and their effects provided insights into the effects of SNPs on miRNA biogenesis and function. The resource data generated in this study will help advance the study of miRNA function and phenotype-associated miRNA identification. BioMed Central 2012-08-21 /pmc/articles/PMC3478155/ /pubmed/22908890 http://dx.doi.org/10.1186/1471-2164-13-413 Text en Copyright ©2012 Zhu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhu, Ya-Ping
Xue, Wei
Wang, Jin-Tu
Wan, Yu-Mei
Wang, Shao-Lin
Xu, Peng
Zhang, Yan
Li, Jiong-Tang
Sun, Xiao-Wen
Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs
title Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs
title_full Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs
title_fullStr Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs
title_full_unstemmed Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs
title_short Identification of common carp (Cyprinus carpio) microRNAs and microRNA-related SNPs
title_sort identification of common carp (cyprinus carpio) micrornas and microrna-related snps
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478155/
https://www.ncbi.nlm.nih.gov/pubmed/22908890
http://dx.doi.org/10.1186/1471-2164-13-413
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