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Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq
Thermal exposure is a serious and growing challenge facing fish species worldwide. Chinook salmon (Oncorhynchus tshawytscha) living in the southern portion of their native range are particularly likely to encounter warmer water due to a confluence of factors. River alterations have increased the lik...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502368/ https://www.ncbi.nlm.nih.gov/pubmed/25911227 http://dx.doi.org/10.1534/g3.115.017699 |
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author | Tomalty, Katharine M. H. Meek, Mariah H. Stephens, Molly R. Rincón, Gonzalo Fangue, Nann A. May, Bernie P. Baerwald, Melinda R. |
author_facet | Tomalty, Katharine M. H. Meek, Mariah H. Stephens, Molly R. Rincón, Gonzalo Fangue, Nann A. May, Bernie P. Baerwald, Melinda R. |
author_sort | Tomalty, Katharine M. H. |
collection | PubMed |
description | Thermal exposure is a serious and growing challenge facing fish species worldwide. Chinook salmon (Oncorhynchus tshawytscha) living in the southern portion of their native range are particularly likely to encounter warmer water due to a confluence of factors. River alterations have increased the likelihood that juveniles will be exposed to warm water temperatures during their freshwater life stage, which can negatively impact survival, growth, and development and pose a threat to dwindling salmon populations. To better understand how acute thermal exposure affects the biology of salmon, we performed a transcriptional analysis of gill tissue from Chinook salmon juveniles reared at 12° and exposed acutely to water temperatures ranging from ideal to potentially lethal (12° to 25°). Reverse-transcribed RNA libraries were sequenced on the Illumina HiSeq2000 platform and a de novo reference transcriptome was created. Differentially expressed transcripts were annotated using Blast2GO and relevant gene clusters were identified. In addition to a high degree of downregulation of a wide range of genes, we found upregulation of genes involved in protein folding/rescue, protein degradation, cell death, oxidative stress, metabolism, inflammation/immunity, transcription/translation, ion transport, cell cycle/growth, cell signaling, cellular trafficking, and structure/cytoskeleton. These results demonstrate the complex multi-modal cellular response to thermal stress in juvenile salmon. |
format | Online Article Text |
id | pubmed-4502368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-45023682015-07-17 Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq Tomalty, Katharine M. H. Meek, Mariah H. Stephens, Molly R. Rincón, Gonzalo Fangue, Nann A. May, Bernie P. Baerwald, Melinda R. G3 (Bethesda) Investigations Thermal exposure is a serious and growing challenge facing fish species worldwide. Chinook salmon (Oncorhynchus tshawytscha) living in the southern portion of their native range are particularly likely to encounter warmer water due to a confluence of factors. River alterations have increased the likelihood that juveniles will be exposed to warm water temperatures during their freshwater life stage, which can negatively impact survival, growth, and development and pose a threat to dwindling salmon populations. To better understand how acute thermal exposure affects the biology of salmon, we performed a transcriptional analysis of gill tissue from Chinook salmon juveniles reared at 12° and exposed acutely to water temperatures ranging from ideal to potentially lethal (12° to 25°). Reverse-transcribed RNA libraries were sequenced on the Illumina HiSeq2000 platform and a de novo reference transcriptome was created. Differentially expressed transcripts were annotated using Blast2GO and relevant gene clusters were identified. In addition to a high degree of downregulation of a wide range of genes, we found upregulation of genes involved in protein folding/rescue, protein degradation, cell death, oxidative stress, metabolism, inflammation/immunity, transcription/translation, ion transport, cell cycle/growth, cell signaling, cellular trafficking, and structure/cytoskeleton. These results demonstrate the complex multi-modal cellular response to thermal stress in juvenile salmon. Genetics Society of America 2015-04-24 /pmc/articles/PMC4502368/ /pubmed/25911227 http://dx.doi.org/10.1534/g3.115.017699 Text en Copyright © 2015 Tomalty et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article 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 the original work is properly cited. |
spellingShingle | Investigations Tomalty, Katharine M. H. Meek, Mariah H. Stephens, Molly R. Rincón, Gonzalo Fangue, Nann A. May, Bernie P. Baerwald, Melinda R. Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq |
title | Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq |
title_full | Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq |
title_fullStr | Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq |
title_full_unstemmed | Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq |
title_short | Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq |
title_sort | transcriptional response to acute thermal exposure in juvenile chinook salmon determined by rnaseq |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502368/ https://www.ncbi.nlm.nih.gov/pubmed/25911227 http://dx.doi.org/10.1534/g3.115.017699 |
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