Cargando…

When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain

BACKGROUND: During long dives, the brain of whales and seals experiences a reduced supply of oxygen (hypoxia). The brain neurons of the hooded seal (Cystophora cristata) are more tolerant towards low-oxygen conditions than those of mice, and also better survive other hypoxia-related stress condition...

Descripción completa

Detalles Bibliográficos
Autores principales: Fabrizius, Andrej, Hoff, Mariana Leivas Müller, Engler, Gerhard, Folkow, Lars P., Burmester, Thorsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979143/
https://www.ncbi.nlm.nih.gov/pubmed/27507242
http://dx.doi.org/10.1186/s12864-016-2892-y
_version_ 1782447277508395008
author Fabrizius, Andrej
Hoff, Mariana Leivas Müller
Engler, Gerhard
Folkow, Lars P.
Burmester, Thorsten
author_facet Fabrizius, Andrej
Hoff, Mariana Leivas Müller
Engler, Gerhard
Folkow, Lars P.
Burmester, Thorsten
author_sort Fabrizius, Andrej
collection PubMed
description BACKGROUND: During long dives, the brain of whales and seals experiences a reduced supply of oxygen (hypoxia). The brain neurons of the hooded seal (Cystophora cristata) are more tolerant towards low-oxygen conditions than those of mice, and also better survive other hypoxia-related stress conditions like a reduction in glucose supply and high concentrations of lactate. Little is known about the molecular mechanisms that support the hypoxia tolerance of the diving brain. RESULTS: Here we employed RNA-seq to approach the molecular basis of the unusual stress tolerance of the seal brain. An Illumina-generated transcriptome of the visual cortex of the hooded seal was compared with that of the ferret (Mustela putorius furo), which served as a terrestrial relative. Gene ontology analyses showed a significant enrichment of transcripts related to translation and aerobic energy production in the ferret but not in the seal brain. Clusterin, an extracellular chaperone, is the most highly expressed gene in the seal brain and fourfold higher than in the ferret or any other mammalian brain transcriptome. The largest difference was found for S100B, a calcium-binding stress protein with pleiotropic function, which was 38-fold enriched in the seal brain. Notably, significant enrichment of S100B mRNA was also found in the transcriptomes of whale brains, but not in the brains of terrestrial mammals. CONCLUSION: Comparative transcriptomics indicates a lower aerobic capacity of the seal brain, which may be interpreted as a general energy saving strategy. Elevated expression of stress-related genes, such as clusterin and S100B, possibly contributes to the remarkable hypoxia tolerance of the brain of the hooded seal. Moreover, high levels of S100B that possibly protect the brain appear to be the result of the convergent adaptation of diving mammals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2892-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4979143
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-49791432016-08-11 When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain Fabrizius, Andrej Hoff, Mariana Leivas Müller Engler, Gerhard Folkow, Lars P. Burmester, Thorsten BMC Genomics Research Article BACKGROUND: During long dives, the brain of whales and seals experiences a reduced supply of oxygen (hypoxia). The brain neurons of the hooded seal (Cystophora cristata) are more tolerant towards low-oxygen conditions than those of mice, and also better survive other hypoxia-related stress conditions like a reduction in glucose supply and high concentrations of lactate. Little is known about the molecular mechanisms that support the hypoxia tolerance of the diving brain. RESULTS: Here we employed RNA-seq to approach the molecular basis of the unusual stress tolerance of the seal brain. An Illumina-generated transcriptome of the visual cortex of the hooded seal was compared with that of the ferret (Mustela putorius furo), which served as a terrestrial relative. Gene ontology analyses showed a significant enrichment of transcripts related to translation and aerobic energy production in the ferret but not in the seal brain. Clusterin, an extracellular chaperone, is the most highly expressed gene in the seal brain and fourfold higher than in the ferret or any other mammalian brain transcriptome. The largest difference was found for S100B, a calcium-binding stress protein with pleiotropic function, which was 38-fold enriched in the seal brain. Notably, significant enrichment of S100B mRNA was also found in the transcriptomes of whale brains, but not in the brains of terrestrial mammals. CONCLUSION: Comparative transcriptomics indicates a lower aerobic capacity of the seal brain, which may be interpreted as a general energy saving strategy. Elevated expression of stress-related genes, such as clusterin and S100B, possibly contributes to the remarkable hypoxia tolerance of the brain of the hooded seal. Moreover, high levels of S100B that possibly protect the brain appear to be the result of the convergent adaptation of diving mammals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2892-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-09 /pmc/articles/PMC4979143/ /pubmed/27507242 http://dx.doi.org/10.1186/s12864-016-2892-y Text en © The Author(s). 2016 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
Fabrizius, Andrej
Hoff, Mariana Leivas Müller
Engler, Gerhard
Folkow, Lars P.
Burmester, Thorsten
When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain
title When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain
title_full When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain
title_fullStr When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain
title_full_unstemmed When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain
title_short When the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain
title_sort when the brain goes diving: transcriptome analysis reveals a reduced aerobic energy metabolism and increased stress proteins in the seal brain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979143/
https://www.ncbi.nlm.nih.gov/pubmed/27507242
http://dx.doi.org/10.1186/s12864-016-2892-y
work_keys_str_mv AT fabriziusandrej whenthebraingoesdivingtranscriptomeanalysisrevealsareducedaerobicenergymetabolismandincreasedstressproteinsinthesealbrain
AT hoffmarianaleivasmuller whenthebraingoesdivingtranscriptomeanalysisrevealsareducedaerobicenergymetabolismandincreasedstressproteinsinthesealbrain
AT englergerhard whenthebraingoesdivingtranscriptomeanalysisrevealsareducedaerobicenergymetabolismandincreasedstressproteinsinthesealbrain
AT folkowlarsp whenthebraingoesdivingtranscriptomeanalysisrevealsareducedaerobicenergymetabolismandincreasedstressproteinsinthesealbrain
AT burmesterthorsten whenthebraingoesdivingtranscriptomeanalysisrevealsareducedaerobicenergymetabolismandincreasedstressproteinsinthesealbrain