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Transcriptomic profiles of Dunaliella salina in response to hypersaline stress
BACKGROUND: Dunaliella salina is a good model organism for studying salt stress. In order to have a global understanding of the expression profiles of Dunaliella salina in response to hypersaline stress, we performed quantitative transcriptomic analysis of Dunaliella salina under hypersaline stress...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998148/ https://www.ncbi.nlm.nih.gov/pubmed/32013861 http://dx.doi.org/10.1186/s12864-020-6507-2 |
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author | He, Qinghua Lin, Yaqiu Tan, Hong Zhou, Yu Wen, Yongli Gan, Jiajia Li, Ruiwen Zhang, Qinglian |
author_facet | He, Qinghua Lin, Yaqiu Tan, Hong Zhou, Yu Wen, Yongli Gan, Jiajia Li, Ruiwen Zhang, Qinglian |
author_sort | He, Qinghua |
collection | PubMed |
description | BACKGROUND: Dunaliella salina is a good model organism for studying salt stress. In order to have a global understanding of the expression profiles of Dunaliella salina in response to hypersaline stress, we performed quantitative transcriptomic analysis of Dunaliella salina under hypersaline stress (2.5 M NaCl) of different time duration by the second and third generation sequencing method. RESULTS: Functional enrichment of the up-regulated genes was used to analyze the expression profiles. The enrichment of photosynthesis was observed, accompanied by enrichments of carbon fixation, pigment biosynthetic process and heme biosynthetic process, which also imply the enhancement of photosynthesis. Genes responsible for starch hydrolysis and glycerol synthesis were significantly up-regulated. The enrichment of biosynthesis of unsaturated fatty acids implies the plasma membrane undergoes changes in desaturation pattern. The enrichment of endocytosis implies the degradation of plasma membrane and might help the synthesis of new glycerophospholipid with unsaturated fatty acids. Co-enrichments of protein synthesis and degradation imply a higher protein turnover rate. The enrichments of spliceosome and protein processing in endoplasmic reticulum imply the enhancement of regulations at post-transcriptional and post-translational level. No up-regulation of any Na(+) or Cl(−) channels or transporters was detected, which implies that the extra exclusion of the ions by membrane transporters is possibly not needed. Voltage gated Na(+) and Cl(−) channels, mechanosensitive ion channel are possible signal receptors of salt stress, and Ca(2+) and MAP kinase pathways might play a role in signal transduction. CONCLUSION: At global transcriptomic level, the response of Dunaliella salina to hypersaline stress is a systematic work, possibly involving enhancements of photosynthesis, carbon fixation, and heme biosynthetic process, acceleration of protein turnover, spliceosome, protein processing in endoplasmic reticulum, and endocytosis, as well as degradation of starch, synthesis of glycerol, membrane lipid desaturation. Altogether, the changes of these biological processes occurred at trancriptomic level will help understand how a new intracellular balance achieved in Dunaliella salina to adapt to hypersaline environment, which are worth being confirmed at the physiological levels. |
format | Online Article Text |
id | pubmed-6998148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69981482020-02-05 Transcriptomic profiles of Dunaliella salina in response to hypersaline stress He, Qinghua Lin, Yaqiu Tan, Hong Zhou, Yu Wen, Yongli Gan, Jiajia Li, Ruiwen Zhang, Qinglian BMC Genomics Research Article BACKGROUND: Dunaliella salina is a good model organism for studying salt stress. In order to have a global understanding of the expression profiles of Dunaliella salina in response to hypersaline stress, we performed quantitative transcriptomic analysis of Dunaliella salina under hypersaline stress (2.5 M NaCl) of different time duration by the second and third generation sequencing method. RESULTS: Functional enrichment of the up-regulated genes was used to analyze the expression profiles. The enrichment of photosynthesis was observed, accompanied by enrichments of carbon fixation, pigment biosynthetic process and heme biosynthetic process, which also imply the enhancement of photosynthesis. Genes responsible for starch hydrolysis and glycerol synthesis were significantly up-regulated. The enrichment of biosynthesis of unsaturated fatty acids implies the plasma membrane undergoes changes in desaturation pattern. The enrichment of endocytosis implies the degradation of plasma membrane and might help the synthesis of new glycerophospholipid with unsaturated fatty acids. Co-enrichments of protein synthesis and degradation imply a higher protein turnover rate. The enrichments of spliceosome and protein processing in endoplasmic reticulum imply the enhancement of regulations at post-transcriptional and post-translational level. No up-regulation of any Na(+) or Cl(−) channels or transporters was detected, which implies that the extra exclusion of the ions by membrane transporters is possibly not needed. Voltage gated Na(+) and Cl(−) channels, mechanosensitive ion channel are possible signal receptors of salt stress, and Ca(2+) and MAP kinase pathways might play a role in signal transduction. CONCLUSION: At global transcriptomic level, the response of Dunaliella salina to hypersaline stress is a systematic work, possibly involving enhancements of photosynthesis, carbon fixation, and heme biosynthetic process, acceleration of protein turnover, spliceosome, protein processing in endoplasmic reticulum, and endocytosis, as well as degradation of starch, synthesis of glycerol, membrane lipid desaturation. Altogether, the changes of these biological processes occurred at trancriptomic level will help understand how a new intracellular balance achieved in Dunaliella salina to adapt to hypersaline environment, which are worth being confirmed at the physiological levels. BioMed Central 2020-02-03 /pmc/articles/PMC6998148/ /pubmed/32013861 http://dx.doi.org/10.1186/s12864-020-6507-2 Text en © The Author(s). 2020 Open AccessThis 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 He, Qinghua Lin, Yaqiu Tan, Hong Zhou, Yu Wen, Yongli Gan, Jiajia Li, Ruiwen Zhang, Qinglian Transcriptomic profiles of Dunaliella salina in response to hypersaline stress |
title | Transcriptomic profiles of Dunaliella salina in response to hypersaline stress |
title_full | Transcriptomic profiles of Dunaliella salina in response to hypersaline stress |
title_fullStr | Transcriptomic profiles of Dunaliella salina in response to hypersaline stress |
title_full_unstemmed | Transcriptomic profiles of Dunaliella salina in response to hypersaline stress |
title_short | Transcriptomic profiles of Dunaliella salina in response to hypersaline stress |
title_sort | transcriptomic profiles of dunaliella salina in response to hypersaline stress |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998148/ https://www.ncbi.nlm.nih.gov/pubmed/32013861 http://dx.doi.org/10.1186/s12864-020-6507-2 |
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