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Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly

Insect metamorphosis is a complex process involving drastic morphological and physiological changes. microRNAs (miRNAs) are a class of endogenous small non-coding RNAs that play key roles in regulating various biological processes, including metamorphosis, by post-transcriptional repression of mRNAs...

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Autores principales: Zhang, Qiang, Dou, Wei, Pan, Deng, Chen, Er-Hu, Niu, Jin-Zhi, Smagghe, Guy, Wang, Jin-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439999/
https://www.ncbi.nlm.nih.gov/pubmed/30967796
http://dx.doi.org/10.3389/fphys.2019.00301
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author Zhang, Qiang
Dou, Wei
Pan, Deng
Chen, Er-Hu
Niu, Jin-Zhi
Smagghe, Guy
Wang, Jin-Jun
author_facet Zhang, Qiang
Dou, Wei
Pan, Deng
Chen, Er-Hu
Niu, Jin-Zhi
Smagghe, Guy
Wang, Jin-Jun
author_sort Zhang, Qiang
collection PubMed
description Insect metamorphosis is a complex process involving drastic morphological and physiological changes. microRNAs (miRNAs) are a class of endogenous small non-coding RNAs that play key roles in regulating various biological processes, including metamorphosis, by post-transcriptional repression of mRNAs. The oriental fruit fly, Bactrocera dorsalis, is one of the most destructive insect pests in many Asian countries and the Pacific Islands. The regulatory role of miRNAs in B. dorsalis metamorphosis is unclear. To better understand the molecular regulatory mechanisms of miRNAs in pupariation, Illumina sequencing of the wandering stage (WS), the late WS and the white puparium stage of B. dorsalis were performed. Two hundred forty-nine miRNAs, including 184 known miRNAs and 65 novel miRNAs, were obtained. Among these miRNAs, 19 miRNAs were differentially expressed in pupariation, and eight miRNAs showed relative high expression levels (>50 TPM), of which five differentially expressed miRNAs (DEMs) had target differentially expressed genes (DEGs) predicted by the expected miRNA–mRNA negative regulation pattern using the Illumina HiSeq data. Four sets of DEMs and their predicted target DEGs were confirmed by qPCR. Of the four miRNAs, two miRNAs were down-regulated: miR-981, which may target pdpc, and Bdo-novel-mir-55, which potentially regulates spsX1, psB/C, and chit3. The other two miRNAs were up-regulated: let-7a-3p, which possibly controls lap, and Bdo-novel-mir-24, which may regulate ipc and sp1/2. This study provides a useful resource to elucidate the regulatory role of miRNAs and understand the molecular mechanisms of metamorphosis.
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spelling pubmed-64399992019-04-09 Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly Zhang, Qiang Dou, Wei Pan, Deng Chen, Er-Hu Niu, Jin-Zhi Smagghe, Guy Wang, Jin-Jun Front Physiol Physiology Insect metamorphosis is a complex process involving drastic morphological and physiological changes. microRNAs (miRNAs) are a class of endogenous small non-coding RNAs that play key roles in regulating various biological processes, including metamorphosis, by post-transcriptional repression of mRNAs. The oriental fruit fly, Bactrocera dorsalis, is one of the most destructive insect pests in many Asian countries and the Pacific Islands. The regulatory role of miRNAs in B. dorsalis metamorphosis is unclear. To better understand the molecular regulatory mechanisms of miRNAs in pupariation, Illumina sequencing of the wandering stage (WS), the late WS and the white puparium stage of B. dorsalis were performed. Two hundred forty-nine miRNAs, including 184 known miRNAs and 65 novel miRNAs, were obtained. Among these miRNAs, 19 miRNAs were differentially expressed in pupariation, and eight miRNAs showed relative high expression levels (>50 TPM), of which five differentially expressed miRNAs (DEMs) had target differentially expressed genes (DEGs) predicted by the expected miRNA–mRNA negative regulation pattern using the Illumina HiSeq data. Four sets of DEMs and their predicted target DEGs were confirmed by qPCR. Of the four miRNAs, two miRNAs were down-regulated: miR-981, which may target pdpc, and Bdo-novel-mir-55, which potentially regulates spsX1, psB/C, and chit3. The other two miRNAs were up-regulated: let-7a-3p, which possibly controls lap, and Bdo-novel-mir-24, which may regulate ipc and sp1/2. This study provides a useful resource to elucidate the regulatory role of miRNAs and understand the molecular mechanisms of metamorphosis. Frontiers Media S.A. 2019-03-22 /pmc/articles/PMC6439999/ /pubmed/30967796 http://dx.doi.org/10.3389/fphys.2019.00301 Text en Copyright © 2019 Zhang, Dou, Pan, Chen, Niu, Smagghe and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Zhang, Qiang
Dou, Wei
Pan, Deng
Chen, Er-Hu
Niu, Jin-Zhi
Smagghe, Guy
Wang, Jin-Jun
Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly
title Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly
title_full Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly
title_fullStr Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly
title_full_unstemmed Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly
title_short Genome-Wide Analysis of MicroRNAs in Relation to Pupariation in Oriental Fruit Fly
title_sort genome-wide analysis of micrornas in relation to pupariation in oriental fruit fly
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439999/
https://www.ncbi.nlm.nih.gov/pubmed/30967796
http://dx.doi.org/10.3389/fphys.2019.00301
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