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Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress

The Kelp grouper Epinephelus moara is one of the most widely consumed and economically important marine fish in China. The species can tolerate a wide range of salinity, but genomic resources are not available, and the molecular mechanisms underlying adaptation to salinity at the transcriptomic leve...

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Autores principales: Gao, Quanxin, Yue, Yanfeng, Min, Minghua, Peng, Shiming, Shi, Zhaohong, Wang, Jinbo, Zhang, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138362/
https://www.ncbi.nlm.nih.gov/pubmed/30460103
http://dx.doi.org/10.1080/19768354.2018.1487335
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author Gao, Quanxin
Yue, Yanfeng
Min, Minghua
Peng, Shiming
Shi, Zhaohong
Wang, Jinbo
Zhang, Tao
author_facet Gao, Quanxin
Yue, Yanfeng
Min, Minghua
Peng, Shiming
Shi, Zhaohong
Wang, Jinbo
Zhang, Tao
author_sort Gao, Quanxin
collection PubMed
description The Kelp grouper Epinephelus moara is one of the most widely consumed and economically important marine fish in China. The species can tolerate a wide range of salinity, but genomic resources are not available, and the molecular mechanisms underlying adaptation to salinity at the transcriptomic level remain largely unclear. In this study, the transcriptomic responses of the liver of E. moara under low salinity were investigated using the Illumina digital gene expression system. After de novo assembly, 499,356 transcripts were generated and contributed 445,068 unigenes. A total of 14, 19, 33 and 3101 genes were differentially expressed following exposure to low salinity stress for 2, 6, 24 and 48 h, respectively. Only two genes were differentially expressed in all groups. Four genes related to metabolism and ambient salinity adaption were randomly selected to validate the differentially expressed genes (DEGs) by real-time PCR. Gene Ontology (GO) and Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway enrichment analysis were used to analyse the functional significance of DEGs, including those responding to salinity through diverse biological processes, cellular components, molecular functions, and pathways associated with metabolic and osmotic responses. This work provides new insight into the response to salinity challenges in E. moara, and the findings expand our knowledge of the molecular basis of metabolic regulation mechanisms in this species. Additionally, the transcriptional data provide a valuable resource for future molecular and genetic studies on E. moara.
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spelling pubmed-61383622018-11-20 Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress Gao, Quanxin Yue, Yanfeng Min, Minghua Peng, Shiming Shi, Zhaohong Wang, Jinbo Zhang, Tao Anim Cells Syst (Seoul) Articles The Kelp grouper Epinephelus moara is one of the most widely consumed and economically important marine fish in China. The species can tolerate a wide range of salinity, but genomic resources are not available, and the molecular mechanisms underlying adaptation to salinity at the transcriptomic level remain largely unclear. In this study, the transcriptomic responses of the liver of E. moara under low salinity were investigated using the Illumina digital gene expression system. After de novo assembly, 499,356 transcripts were generated and contributed 445,068 unigenes. A total of 14, 19, 33 and 3101 genes were differentially expressed following exposure to low salinity stress for 2, 6, 24 and 48 h, respectively. Only two genes were differentially expressed in all groups. Four genes related to metabolism and ambient salinity adaption were randomly selected to validate the differentially expressed genes (DEGs) by real-time PCR. Gene Ontology (GO) and Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway enrichment analysis were used to analyse the functional significance of DEGs, including those responding to salinity through diverse biological processes, cellular components, molecular functions, and pathways associated with metabolic and osmotic responses. This work provides new insight into the response to salinity challenges in E. moara, and the findings expand our knowledge of the molecular basis of metabolic regulation mechanisms in this species. Additionally, the transcriptional data provide a valuable resource for future molecular and genetic studies on E. moara. Taylor & Francis 2018-08-22 /pmc/articles/PMC6138362/ /pubmed/30460103 http://dx.doi.org/10.1080/19768354.2018.1487335 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 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 work is properly cited.
spellingShingle Articles
Gao, Quanxin
Yue, Yanfeng
Min, Minghua
Peng, Shiming
Shi, Zhaohong
Wang, Jinbo
Zhang, Tao
Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress
title Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress
title_full Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress
title_fullStr Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress
title_full_unstemmed Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress
title_short Time-series transcriptomic analysis of the kelp grouper Epinephelus moara in response to low salinity stress
title_sort time-series transcriptomic analysis of the kelp grouper epinephelus moara in response to low salinity stress
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138362/
https://www.ncbi.nlm.nih.gov/pubmed/30460103
http://dx.doi.org/10.1080/19768354.2018.1487335
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