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Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes
Chrysanthemum crassum is a decaploid species of Chrysanthemum with high stress tolerance that allows survival under salinity stress while maintaining a relatively ideal growth rate. We previously recorded morphological changes after salt treatment, such as the expansion of leaf cells. To explore the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402956/ https://www.ncbi.nlm.nih.gov/pubmed/28437448 http://dx.doi.org/10.1371/journal.pone.0175972 |
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author | Guan, Zhiyong Feng, Yitong Song, Aiping Shi, Xiaomeng Mao, Yachao Chen, Sumei Jiang, Jiafu Ding, Lian Chen, Fadi |
author_facet | Guan, Zhiyong Feng, Yitong Song, Aiping Shi, Xiaomeng Mao, Yachao Chen, Sumei Jiang, Jiafu Ding, Lian Chen, Fadi |
author_sort | Guan, Zhiyong |
collection | PubMed |
description | Chrysanthemum crassum is a decaploid species of Chrysanthemum with high stress tolerance that allows survival under salinity stress while maintaining a relatively ideal growth rate. We previously recorded morphological changes after salt treatment, such as the expansion of leaf cells. To explore the underlying salinity tolerance mechanisms, we used an Illumina platform and obtained three sequencing libraries from samples collected after 0 h, 12 h and 24 h of salt treatment. Following de novo assembly, 154,944 transcripts were generated, and 97,833 (63.14%) transcripts were annotated, including 55 Gene Ontology (GO) terms and 128 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. The expression profile of C. crassum was globally altered after salt treatment. We selected functional genes and pathways that may contribute to salinity tolerance and identified some factors involved in the salinity tolerance strategies of C. crassum, such as signal transduction, transcription factors and plant hormone regulation, enhancement of energy metabolism, functional proteins and osmolyte synthesis, reactive oxygen species (ROS) scavenging, photosystem protection and recovery, and cell wall protein modifications. Forty-six genes were selected for quantitative real-time polymerase chain reaction detection, and their expression patterns were shown to be consistent with the changes in their transcript abundance determined by RNA sequencing. |
format | Online Article Text |
id | pubmed-5402956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54029562017-05-12 Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes Guan, Zhiyong Feng, Yitong Song, Aiping Shi, Xiaomeng Mao, Yachao Chen, Sumei Jiang, Jiafu Ding, Lian Chen, Fadi PLoS One Research Article Chrysanthemum crassum is a decaploid species of Chrysanthemum with high stress tolerance that allows survival under salinity stress while maintaining a relatively ideal growth rate. We previously recorded morphological changes after salt treatment, such as the expansion of leaf cells. To explore the underlying salinity tolerance mechanisms, we used an Illumina platform and obtained three sequencing libraries from samples collected after 0 h, 12 h and 24 h of salt treatment. Following de novo assembly, 154,944 transcripts were generated, and 97,833 (63.14%) transcripts were annotated, including 55 Gene Ontology (GO) terms and 128 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. The expression profile of C. crassum was globally altered after salt treatment. We selected functional genes and pathways that may contribute to salinity tolerance and identified some factors involved in the salinity tolerance strategies of C. crassum, such as signal transduction, transcription factors and plant hormone regulation, enhancement of energy metabolism, functional proteins and osmolyte synthesis, reactive oxygen species (ROS) scavenging, photosystem protection and recovery, and cell wall protein modifications. Forty-six genes were selected for quantitative real-time polymerase chain reaction detection, and their expression patterns were shown to be consistent with the changes in their transcript abundance determined by RNA sequencing. Public Library of Science 2017-04-24 /pmc/articles/PMC5402956/ /pubmed/28437448 http://dx.doi.org/10.1371/journal.pone.0175972 Text en © 2017 Guan 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 Guan, Zhiyong Feng, Yitong Song, Aiping Shi, Xiaomeng Mao, Yachao Chen, Sumei Jiang, Jiafu Ding, Lian Chen, Fadi Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes |
title | Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes |
title_full | Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes |
title_fullStr | Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes |
title_full_unstemmed | Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes |
title_short | Expression profiling of Chrysanthemum crassum under salinity stress and the initiation of morphological changes |
title_sort | expression profiling of chrysanthemum crassum under salinity stress and the initiation of morphological changes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402956/ https://www.ncbi.nlm.nih.gov/pubmed/28437448 http://dx.doi.org/10.1371/journal.pone.0175972 |
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