Cargando…

Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis

BACKGROUND: MicroRNAs (miRNAs) are a class of noncoding small RNAs (sRNAs) that are 20–24 nucleotides (nt) in length. Extensive studies have indicated that miRNAs play versatile roles in plants, functioning in processes such as growth, development and stress responses. Chilling is a common abiotic s...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Xue, Wu, Zhen, Jiang, Fangling, Zhou, Rong, Yang, Zeen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377850/
https://www.ncbi.nlm.nih.gov/pubmed/25519760
http://dx.doi.org/10.1186/1471-2164-15-1130
_version_ 1782363970800189440
author Cao, Xue
Wu, Zhen
Jiang, Fangling
Zhou, Rong
Yang, Zeen
author_facet Cao, Xue
Wu, Zhen
Jiang, Fangling
Zhou, Rong
Yang, Zeen
author_sort Cao, Xue
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) are a class of noncoding small RNAs (sRNAs) that are 20–24 nucleotides (nt) in length. Extensive studies have indicated that miRNAs play versatile roles in plants, functioning in processes such as growth, development and stress responses. Chilling is a common abiotic stress that seriously affects plants growth and development. Recently, chilling-responsive miRNAs have been detected in several plant species. However, little is known about the miRNAs in the model plant tomato. ‘LA1777’ (Solanum habrochaites) has been shown to survive chilling stress due to its various characteristics. RESULTS: Here, two small RNA libraries and two degradome libraries were produced from chilling-treated (CT) and non-chilling-treated (NT) leaves of S. habrochaites seedlings. Following high-throughput sequencing and filtering, 161 conserved and 236 novel miRNAs were identified in the two libraries. Of these miRNAs, 192 increased in the response to chilling stress while 205 decreased. Furthermore, the target genes of the miRNAs were predicted using a degradome sequencing approach. It was found that 62 target genes were cleaved by 42 conserved miRNAs, while nine target genes were cleaved by nine novel miRNAs. Additionally, nine miRNAs and six target genes were validated by quantitative real-time PCR (qRT-PCR). Target gene functional analysis showed that most target genes played positive roles in the chilling response, primarily by regulating the expression of anti-stress proteins, antioxidant enzyme and genes involved in cell wall formation. CONCLUSIONS: Tomato is an important model plant for basic biological research. In this study, numerous conserved and novel miRNAs involved in the chilling response were identified using high-throughput sequencing, and the target genes were analyzed by degradome sequencing. The work helps identify chilling-responsive miRNAs in tomato and increases the number of identified miRNAs involved in chilling stress. Furthermore, the work provides a foundation for further study of the regulation of miRNAs in the plant response to chilling stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-1130) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4377850
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-43778502015-03-31 Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis Cao, Xue Wu, Zhen Jiang, Fangling Zhou, Rong Yang, Zeen BMC Genomics Research Article BACKGROUND: MicroRNAs (miRNAs) are a class of noncoding small RNAs (sRNAs) that are 20–24 nucleotides (nt) in length. Extensive studies have indicated that miRNAs play versatile roles in plants, functioning in processes such as growth, development and stress responses. Chilling is a common abiotic stress that seriously affects plants growth and development. Recently, chilling-responsive miRNAs have been detected in several plant species. However, little is known about the miRNAs in the model plant tomato. ‘LA1777’ (Solanum habrochaites) has been shown to survive chilling stress due to its various characteristics. RESULTS: Here, two small RNA libraries and two degradome libraries were produced from chilling-treated (CT) and non-chilling-treated (NT) leaves of S. habrochaites seedlings. Following high-throughput sequencing and filtering, 161 conserved and 236 novel miRNAs were identified in the two libraries. Of these miRNAs, 192 increased in the response to chilling stress while 205 decreased. Furthermore, the target genes of the miRNAs were predicted using a degradome sequencing approach. It was found that 62 target genes were cleaved by 42 conserved miRNAs, while nine target genes were cleaved by nine novel miRNAs. Additionally, nine miRNAs and six target genes were validated by quantitative real-time PCR (qRT-PCR). Target gene functional analysis showed that most target genes played positive roles in the chilling response, primarily by regulating the expression of anti-stress proteins, antioxidant enzyme and genes involved in cell wall formation. CONCLUSIONS: Tomato is an important model plant for basic biological research. In this study, numerous conserved and novel miRNAs involved in the chilling response were identified using high-throughput sequencing, and the target genes were analyzed by degradome sequencing. The work helps identify chilling-responsive miRNAs in tomato and increases the number of identified miRNAs involved in chilling stress. Furthermore, the work provides a foundation for further study of the regulation of miRNAs in the plant response to chilling stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-1130) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-17 /pmc/articles/PMC4377850/ /pubmed/25519760 http://dx.doi.org/10.1186/1471-2164-15-1130 Text en © Cao et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. 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 Article
Cao, Xue
Wu, Zhen
Jiang, Fangling
Zhou, Rong
Yang, Zeen
Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis
title Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis
title_full Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis
title_fullStr Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis
title_full_unstemmed Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis
title_short Identification of chilling stress-responsive tomato microRNAs and their target genes by high-throughput sequencing and degradome analysis
title_sort identification of chilling stress-responsive tomato micrornas and their target genes by high-throughput sequencing and degradome analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377850/
https://www.ncbi.nlm.nih.gov/pubmed/25519760
http://dx.doi.org/10.1186/1471-2164-15-1130
work_keys_str_mv AT caoxue identificationofchillingstressresponsivetomatomicrornasandtheirtargetgenesbyhighthroughputsequencinganddegradomeanalysis
AT wuzhen identificationofchillingstressresponsivetomatomicrornasandtheirtargetgenesbyhighthroughputsequencinganddegradomeanalysis
AT jiangfangling identificationofchillingstressresponsivetomatomicrornasandtheirtargetgenesbyhighthroughputsequencinganddegradomeanalysis
AT zhourong identificationofchillingstressresponsivetomatomicrornasandtheirtargetgenesbyhighthroughputsequencinganddegradomeanalysis
AT yangzeen identificationofchillingstressresponsivetomatomicrornasandtheirtargetgenesbyhighthroughputsequencinganddegradomeanalysis