Background: Many fish species experience long periods of fasting in nature often associated with seasonal reductions in water temperature and prey availability or spawning migrations. During periods of nutrient restriction, changes in metabolism occur to provide cellular energy via catabolic processes. Muscle is particularly affected by prolonged fasting as myofibrillar proteins act as a major energy source. To investigate the mechanisms of metabolic reorganisation with fasting and refeeding in a saltwater stage of Atlantic salmon (Salmo salar L.) we analysed the expression of genes involved in myogenesis, growth signalling, lipid biosynthesis and myofibrillar protein degradation and synthesis pathways using qPCR. Results: Hierarchical clustering of gene expression data revealed three clusters. The first cluster comprised genes involved in lipid metabolism and triacylglycerol synthesis (ALDOB, DGAT1 and LPL) which had peak expression 3-14d after refeeding. The second cluster comprised ADIPOQ, MLC2, IGF-I and TALDO1, with peak expression 14-32d after refeeding. Cluster III contained genes strongly down regulated as an initial response to feeding and included the ubiquitin ligases MuRF1 and MAFbx, myogenic regulatory factors and some metabolic genes. Conclusion: Early responses to refeeding in fasted salmon included the synthesis of triacylglycerols and activation of the adipogenic differentiation program. Inhibition of MuRF1 and MAFbx respectively may result in decreased degradation and concomitant increased production of myofibrillar proteins. Both of these processes preceded any increase in expression of myogenic regulatory factors and IGF-I. These responses could be a necessary strategy for an animal adapted to long periods of food deprivation whereby energy reserves are replenished prior to the resumption of myogenesis.
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Barts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, EnglandBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Bustin, Stephen A.
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Benes, Vladimir
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EMBL Heidelberg, Genom Core Facil, Heidelberg, GermanyBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Benes, Vladimir
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Garson, Jeremy A.
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UCL, Dept Infect, Ctr Virol, London, England
UCL Hosp, NHS Fdn Trust, Dept Virol, London, EnglandBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Garson, Jeremy A.
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Hellemans, Jan
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Huggett, Jim
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UCL, Ctr Infect Dis, London, EnglandBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Huggett, Jim
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Kubista, Mikael
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TATAA Bioctr, Gothenburg, Sweden
Inst Biotechnol AS CR, Prague, Czech RepublicBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Kubista, Mikael
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Mueller, Reinhold
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Sequenom, San Diego, CA USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Mueller, Reinhold
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Nolan, Tania
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Sigma Aldrich, Haverhill, MA USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Nolan, Tania
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Pfaffl, Michael W.
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Tech Univ Munich, D-8050 Freising Weihenstephan, GermanyBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Pfaffl, Michael W.
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Shipley, Gregory L.
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Univ Texas Houston, Hlth Sci Ctr, Dept Integrat Biol & Pharmacol, Quantitat Genom Core Lab, Houston, TX USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Shipley, Gregory L.
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Vandesompele, Jo
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Wittwer, Carl T.
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Univ Utah, Dept Pathol, Salt Lake City, UT USA
ARUP Inst Clin & Expt Pathol, Salt Lake City, UT USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
机构:
Barts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, EnglandBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Bustin, Stephen A.
;
Benes, Vladimir
论文数: 0引用数: 0
h-index: 0
机构:
EMBL Heidelberg, Genom Core Facil, Heidelberg, GermanyBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Benes, Vladimir
;
Garson, Jeremy A.
论文数: 0引用数: 0
h-index: 0
机构:
UCL, Dept Infect, Ctr Virol, London, England
UCL Hosp, NHS Fdn Trust, Dept Virol, London, EnglandBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Garson, Jeremy A.
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Hellemans, Jan
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Huggett, Jim
论文数: 0引用数: 0
h-index: 0
机构:
UCL, Ctr Infect Dis, London, EnglandBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Huggett, Jim
;
Kubista, Mikael
论文数: 0引用数: 0
h-index: 0
机构:
TATAA Bioctr, Gothenburg, Sweden
Inst Biotechnol AS CR, Prague, Czech RepublicBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Kubista, Mikael
;
Mueller, Reinhold
论文数: 0引用数: 0
h-index: 0
机构:
Sequenom, San Diego, CA USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Mueller, Reinhold
;
Nolan, Tania
论文数: 0引用数: 0
h-index: 0
机构:
Sigma Aldrich, Haverhill, MA USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Nolan, Tania
;
Pfaffl, Michael W.
论文数: 0引用数: 0
h-index: 0
机构:
Tech Univ Munich, D-8050 Freising Weihenstephan, GermanyBarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Pfaffl, Michael W.
;
Shipley, Gregory L.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Texas Houston, Hlth Sci Ctr, Dept Integrat Biol & Pharmacol, Quantitat Genom Core Lab, Houston, TX USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England
Shipley, Gregory L.
;
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h-index:
机构:
Vandesompele, Jo
;
Wittwer, Carl T.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Utah, Dept Pathol, Salt Lake City, UT USA
ARUP Inst Clin & Expt Pathol, Salt Lake City, UT USABarts & London Queen Marys Sch Med & Dent, Inst Cell & Mol Sci, Ctr Acad Surg, London, England