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Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes

BACKGROUND: Anuran metamorphosis, which is obligatorily initiated and sustained by thyroid hormone (TH), is a dramatic example of extensive morphological, biochemical and cellular changes occurring during post-embryonic development. Thus, it provides an ideal model to understand the actions of the h...

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Autores principales: Liu, Lusha, Zhu, Wei, Liu, Jiongyu, Wang, Shouhong, Jiang, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025837/
https://www.ncbi.nlm.nih.gov/pubmed/29954327
http://dx.doi.org/10.1186/s12864-018-4848-x
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author Liu, Lusha
Zhu, Wei
Liu, Jiongyu
Wang, Shouhong
Jiang, Jianping
author_facet Liu, Lusha
Zhu, Wei
Liu, Jiongyu
Wang, Shouhong
Jiang, Jianping
author_sort Liu, Lusha
collection PubMed
description BACKGROUND: Anuran metamorphosis, which is obligatorily initiated and sustained by thyroid hormone (TH), is a dramatic example of extensive morphological, biochemical and cellular changes occurring during post-embryonic development. Thus, it provides an ideal model to understand the actions of the hormone and molecular mechanisms underlying these developmental and apoptotic processes. In addition to transcriptional factors, microRNAs (miRNAs) play key roles in diverse biological processes via post-transcriptional repression of mRNAs. However, the possible role of miRNAs in anuran metamorphosis is not well understood. Screening and identification of TH-responding miRNAs are required to reveal the integrated regulatory mechanisms of TH during metamorphosis. Given the specific role of TRs during M. fissipes metamorphosis and the characteristics of M. fissipes as an ideal model, Illumina sequencing technology was employed to get a full scope of miRNA in M. fissipes metamorphosis treated by T3. RESULTS: Morphological and histological analysis revealed that 24 h T3 treatment M. fissipes tadpoles resembled that at the climax of natural metamorphosis. Thus, small RNA libraries were constructed from control and 24 h T3 treatment groups. A total of 164 conserved miRNAs and 36 predicted novel miRNAs were characterized. Furthermore, 5′ first and ninth nucleotides of miRNAs were significantly enriched in U in our study. In all, 21 miRNAs were differentially expressed between the T3 and control groups (p < 0.01). A total of 10,206 unigenes were identified as target genes of these differentially expressed miRNAs. KEGG pathway analysis indicated that the most overrepresented miRNA target genes were enriched in the “PI3k-Akt signaling pathway”. In addition, a network associated with the TH signaling pathway provides an opportunity to further understand the complex biological processes that occur in metamorphosis. CONCLUSIONS: We identified a large number of miRNAs during M. fissipes metamorphosis, and 21 of them were differentially expressed in the two groups that represented two different metamorphic stages. These miRNAs may play important roles during metamorphosis. The study gives us clues for further studies of the mechanisms of anuran metamorphosis and provides a model to study the mechanism of TH-affected biological processes in humans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4848-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-60258372018-07-09 Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes Liu, Lusha Zhu, Wei Liu, Jiongyu Wang, Shouhong Jiang, Jianping BMC Genomics Research Article BACKGROUND: Anuran metamorphosis, which is obligatorily initiated and sustained by thyroid hormone (TH), is a dramatic example of extensive morphological, biochemical and cellular changes occurring during post-embryonic development. Thus, it provides an ideal model to understand the actions of the hormone and molecular mechanisms underlying these developmental and apoptotic processes. In addition to transcriptional factors, microRNAs (miRNAs) play key roles in diverse biological processes via post-transcriptional repression of mRNAs. However, the possible role of miRNAs in anuran metamorphosis is not well understood. Screening and identification of TH-responding miRNAs are required to reveal the integrated regulatory mechanisms of TH during metamorphosis. Given the specific role of TRs during M. fissipes metamorphosis and the characteristics of M. fissipes as an ideal model, Illumina sequencing technology was employed to get a full scope of miRNA in M. fissipes metamorphosis treated by T3. RESULTS: Morphological and histological analysis revealed that 24 h T3 treatment M. fissipes tadpoles resembled that at the climax of natural metamorphosis. Thus, small RNA libraries were constructed from control and 24 h T3 treatment groups. A total of 164 conserved miRNAs and 36 predicted novel miRNAs were characterized. Furthermore, 5′ first and ninth nucleotides of miRNAs were significantly enriched in U in our study. In all, 21 miRNAs were differentially expressed between the T3 and control groups (p < 0.01). A total of 10,206 unigenes were identified as target genes of these differentially expressed miRNAs. KEGG pathway analysis indicated that the most overrepresented miRNA target genes were enriched in the “PI3k-Akt signaling pathway”. In addition, a network associated with the TH signaling pathway provides an opportunity to further understand the complex biological processes that occur in metamorphosis. CONCLUSIONS: We identified a large number of miRNAs during M. fissipes metamorphosis, and 21 of them were differentially expressed in the two groups that represented two different metamorphic stages. These miRNAs may play important roles during metamorphosis. The study gives us clues for further studies of the mechanisms of anuran metamorphosis and provides a model to study the mechanism of TH-affected biological processes in humans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4848-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-28 /pmc/articles/PMC6025837/ /pubmed/29954327 http://dx.doi.org/10.1186/s12864-018-4848-x Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article
Liu, Lusha
Zhu, Wei
Liu, Jiongyu
Wang, Shouhong
Jiang, Jianping
Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes
title Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes
title_full Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes
title_fullStr Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes
title_full_unstemmed Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes
title_short Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes
title_sort identification and differential regulation of micrornas during thyroid hormone-dependent metamorphosis in microhyla fissipes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025837/
https://www.ncbi.nlm.nih.gov/pubmed/29954327
http://dx.doi.org/10.1186/s12864-018-4848-x
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