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High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba)
MicroRNAs (miRNAs) play important regulatory roles by targeting mRNAs for cleavage or translational repression. Identification of miRNA targets is essential to better understanding the roles of miRNAs. miRNA targets have not been well characterized in mulberry (Morus alba). To anatomize miRNA guided...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325578/ https://www.ncbi.nlm.nih.gov/pubmed/28235056 http://dx.doi.org/10.1371/journal.pone.0172883 |
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author | Li, Ruixue Chen, Dandan Wang, Taichu Wan, Yizhen Li, Rongfang Fang, Rongjun Wang, Yuting Hu, Fei Zhou, Hong Li, Long Zhao, Weiguo |
author_facet | Li, Ruixue Chen, Dandan Wang, Taichu Wan, Yizhen Li, Rongfang Fang, Rongjun Wang, Yuting Hu, Fei Zhou, Hong Li, Long Zhao, Weiguo |
author_sort | Li, Ruixue |
collection | PubMed |
description | MicroRNAs (miRNAs) play important regulatory roles by targeting mRNAs for cleavage or translational repression. Identification of miRNA targets is essential to better understanding the roles of miRNAs. miRNA targets have not been well characterized in mulberry (Morus alba). To anatomize miRNA guided gene regulation under drought stress, transcriptome-wide high throughput degradome sequencing was used in this study to directly detect drought stress responsive miRNA targets in mulberry. A drought library (DL) and a contrast library (CL) were constructed to capture the cleaved mRNAs for sequencing. In CL, 409 target genes of 30 conserved miRNA families and 990 target genes of 199 novel miRNAs were identified. In DL, 373 target genes of 30 conserved miRNA families and 950 target genes of 195 novel miRNAs were identified. Of the conserved miRNA families in DL, mno-miR156, mno-miR172, and mno-miR396 had the highest number of targets with 54, 52 and 41 transcripts, respectively, indicating that these three miRNA families and their target genes might play important functions in response to drought stress in mulberry. Additionally, we found that many of the target genes were transcription factors. By analyzing the miRNA-target molecular network, we found that the DL independent networks consisted of 838 miRNA-mRNA pairs (63.34%). The expression patterns of 11 target genes and 12 correspondent miRNAs were detected using qRT-PCR. Six miRNA targets were further verified by RNA ligase-mediated 5’ rapid amplification of cDNA ends (RLM-5’ RACE). Gene Ontology (GO) annotations and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed that these target transcripts were implicated in a broad range of biological processes and various metabolic pathways. This is the first study to comprehensively characterize target genes and their associated miRNAs in response to drought stress by degradome sequencing in mulberry. This study provides a framework for understanding the molecular mechanisms of drought resistance in mulberry. |
format | Online Article Text |
id | pubmed-5325578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53255782017-03-09 High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba) Li, Ruixue Chen, Dandan Wang, Taichu Wan, Yizhen Li, Rongfang Fang, Rongjun Wang, Yuting Hu, Fei Zhou, Hong Li, Long Zhao, Weiguo PLoS One Research Article MicroRNAs (miRNAs) play important regulatory roles by targeting mRNAs for cleavage or translational repression. Identification of miRNA targets is essential to better understanding the roles of miRNAs. miRNA targets have not been well characterized in mulberry (Morus alba). To anatomize miRNA guided gene regulation under drought stress, transcriptome-wide high throughput degradome sequencing was used in this study to directly detect drought stress responsive miRNA targets in mulberry. A drought library (DL) and a contrast library (CL) were constructed to capture the cleaved mRNAs for sequencing. In CL, 409 target genes of 30 conserved miRNA families and 990 target genes of 199 novel miRNAs were identified. In DL, 373 target genes of 30 conserved miRNA families and 950 target genes of 195 novel miRNAs were identified. Of the conserved miRNA families in DL, mno-miR156, mno-miR172, and mno-miR396 had the highest number of targets with 54, 52 and 41 transcripts, respectively, indicating that these three miRNA families and their target genes might play important functions in response to drought stress in mulberry. Additionally, we found that many of the target genes were transcription factors. By analyzing the miRNA-target molecular network, we found that the DL independent networks consisted of 838 miRNA-mRNA pairs (63.34%). The expression patterns of 11 target genes and 12 correspondent miRNAs were detected using qRT-PCR. Six miRNA targets were further verified by RNA ligase-mediated 5’ rapid amplification of cDNA ends (RLM-5’ RACE). Gene Ontology (GO) annotations and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed that these target transcripts were implicated in a broad range of biological processes and various metabolic pathways. This is the first study to comprehensively characterize target genes and their associated miRNAs in response to drought stress by degradome sequencing in mulberry. This study provides a framework for understanding the molecular mechanisms of drought resistance in mulberry. Public Library of Science 2017-02-24 /pmc/articles/PMC5325578/ /pubmed/28235056 http://dx.doi.org/10.1371/journal.pone.0172883 Text en © 2017 Li et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited. |
spellingShingle | Research Article Li, Ruixue Chen, Dandan Wang, Taichu Wan, Yizhen Li, Rongfang Fang, Rongjun Wang, Yuting Hu, Fei Zhou, Hong Li, Long Zhao, Weiguo High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba) |
title | High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba) |
title_full | High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba) |
title_fullStr | High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba) |
title_full_unstemmed | High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba) |
title_short | High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba) |
title_sort | high throughput deep degradome sequencing reveals micrornas and their targets in response to drought stress in mulberry (morus alba) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325578/ https://www.ncbi.nlm.nih.gov/pubmed/28235056 http://dx.doi.org/10.1371/journal.pone.0172883 |
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