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Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients

BACKGROUND: Circannual rhythms in vertebrates can influence a wide variety of physiological processes. Some notable examples include annual reproductive cycles and for poikilotherms, seasonal changes modulating growth. Increasing water temperature elevates growth rates in fishes, but increases in ph...

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Autores principales: Danzmann, Roy G., Kocmarek, Andrea L., Norman, Joseph D., Rexroad, Caird E., Palti, Yniv
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714434/
https://www.ncbi.nlm.nih.gov/pubmed/26768650
http://dx.doi.org/10.1186/s12864-016-2363-5
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author Danzmann, Roy G.
Kocmarek, Andrea L.
Norman, Joseph D.
Rexroad, Caird E.
Palti, Yniv
author_facet Danzmann, Roy G.
Kocmarek, Andrea L.
Norman, Joseph D.
Rexroad, Caird E.
Palti, Yniv
author_sort Danzmann, Roy G.
collection PubMed
description BACKGROUND: Circannual rhythms in vertebrates can influence a wide variety of physiological processes. Some notable examples include annual reproductive cycles and for poikilotherms, seasonal changes modulating growth. Increasing water temperature elevates growth rates in fishes, but increases in photoperiod regime can have similar influences even at constant temperature. Therefore, in order to understand the dynamics of growth in fish it is important to consider the background influence of photoperiod regime on gene expression differences. This study examined the influence of a declining photoperiod regime (winter solstice) compared to an increasing photoperiod regime (spring equinox) on white muscle transcriptome profiles in fast and slow-growing rainbow trout from a commercial aquaculture strain. RESULTS: Slow-growing fish could be characterized as possessing transcriptome profiles that conform in many respects to an endurance training regime in humans. They have elevated mitochondrial and cytosolic creatine kinase expression levels and appear to suppress mTOR-signaling as evidenced by elevated TSC2 expression, and they also have elevated p53 levels. Large fish display a physiological repertoire that may be consistent with strength/resistance physiology having elevated cytoskeletal gene component expression and glycogen metabolism cycling along with higher PI3K levels. In many respects small vs. large fish match eccentric vs. concentric muscle expression patterns, respectively. Lipid metabolic genes are also more elevated in larger fish, the most notable being the G0S2 switch gene. M and Z-line sarcomere remodelling appears to be more prevalent in large fish. Twenty-three out of 26 gene families with previously reported significant SNP-based growth differences were detected as having significant expression differences. CONCLUSIONS: Larger fish display a broader array of genes showing higher expression, and their profiles are more similar to those observed in December lot fish (i.e., an accelerated growth period). Conversely, small fish display gene profiles more similar to seasonal growth decline phases (i.e., September lot fish). Overall, seasonal timing was coupled to greater differences in gene expression compared to differences associated with fish size. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2363-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-47144342016-01-16 Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients Danzmann, Roy G. Kocmarek, Andrea L. Norman, Joseph D. Rexroad, Caird E. Palti, Yniv BMC Genomics Research Article BACKGROUND: Circannual rhythms in vertebrates can influence a wide variety of physiological processes. Some notable examples include annual reproductive cycles and for poikilotherms, seasonal changes modulating growth. Increasing water temperature elevates growth rates in fishes, but increases in photoperiod regime can have similar influences even at constant temperature. Therefore, in order to understand the dynamics of growth in fish it is important to consider the background influence of photoperiod regime on gene expression differences. This study examined the influence of a declining photoperiod regime (winter solstice) compared to an increasing photoperiod regime (spring equinox) on white muscle transcriptome profiles in fast and slow-growing rainbow trout from a commercial aquaculture strain. RESULTS: Slow-growing fish could be characterized as possessing transcriptome profiles that conform in many respects to an endurance training regime in humans. They have elevated mitochondrial and cytosolic creatine kinase expression levels and appear to suppress mTOR-signaling as evidenced by elevated TSC2 expression, and they also have elevated p53 levels. Large fish display a physiological repertoire that may be consistent with strength/resistance physiology having elevated cytoskeletal gene component expression and glycogen metabolism cycling along with higher PI3K levels. In many respects small vs. large fish match eccentric vs. concentric muscle expression patterns, respectively. Lipid metabolic genes are also more elevated in larger fish, the most notable being the G0S2 switch gene. M and Z-line sarcomere remodelling appears to be more prevalent in large fish. Twenty-three out of 26 gene families with previously reported significant SNP-based growth differences were detected as having significant expression differences. CONCLUSIONS: Larger fish display a broader array of genes showing higher expression, and their profiles are more similar to those observed in December lot fish (i.e., an accelerated growth period). Conversely, small fish display gene profiles more similar to seasonal growth decline phases (i.e., September lot fish). Overall, seasonal timing was coupled to greater differences in gene expression compared to differences associated with fish size. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2363-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-15 /pmc/articles/PMC4714434/ /pubmed/26768650 http://dx.doi.org/10.1186/s12864-016-2363-5 Text en © Danzmann et al. 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
Danzmann, Roy G.
Kocmarek, Andrea L.
Norman, Joseph D.
Rexroad, Caird E.
Palti, Yniv
Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients
title Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients
title_full Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients
title_fullStr Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients
title_full_unstemmed Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients
title_short Transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients
title_sort transcriptome profiling in fast versus slow-growing rainbow trout across seasonal gradients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714434/
https://www.ncbi.nlm.nih.gov/pubmed/26768650
http://dx.doi.org/10.1186/s12864-016-2363-5
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