Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon

Abstract 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...

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Main Authors: Bower, Neil I, Taylor, Richard G, Johnston, Ian A
Format: Other/Unknown Material
Language:English
Published: BioMed Central Ltd. 2009
Subjects:
Online Access:http://www.frontiersinzoology.com/content/6/1/18
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spelling ftbiomed:oai:biomedcentral.com:1742-9994-6-18 2023-05-15T15:31:44+02:00 Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon Bower, Neil I Taylor, Richard G Johnston, Ian A 2009-08-24 http://www.frontiersinzoology.com/content/6/1/18 en eng BioMed Central Ltd. http://www.frontiersinzoology.com/content/6/1/18 Copyright 2009 Bower et al; licensee BioMed Central Ltd. Research 2009 ftbiomed 2009-09-25T23:23:16Z Abstract 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. Other/Unknown Material Atlantic salmon Salmo salar BioMed Central
institution Open Polar
collection BioMed Central
op_collection_id ftbiomed
language English
description Abstract 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.
format Other/Unknown Material
author Bower, Neil I
Taylor, Richard G
Johnston, Ian A
spellingShingle Bower, Neil I
Taylor, Richard G
Johnston, Ian A
Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon
author_facet Bower, Neil I
Taylor, Richard G
Johnston, Ian A
author_sort Bower, Neil I
title Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon
title_short Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon
title_full Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon
title_fullStr Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon
title_full_unstemmed Phasing of muscle gene expression with fasting-induced recovery growth in Atlantic salmon
title_sort phasing of muscle gene expression with fasting-induced recovery growth in atlantic salmon
publisher BioMed Central Ltd.
publishDate 2009
url http://www.frontiersinzoology.com/content/6/1/18
genre Atlantic salmon
Salmo salar
genre_facet Atlantic salmon
Salmo salar
op_relation http://www.frontiersinzoology.com/content/6/1/18
op_rights Copyright 2009 Bower et al; licensee BioMed Central Ltd.
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