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

被引:60
作者
Bower, Neil I. [1 ]
Taylor, Richard G. [2 ]
Johnston, Ian A. [1 ]
机构
[1] Univ St Andrews, Sch Biol, Gatty Marine Lab, St Andrews KY16 8LB, Fife, Scotland
[2] EWOS Innovat, N-4335 Dirdal, Norway
关键词
SKELETAL-MUSCLE; REGULATORY FACTORS; ENERGY-METABOLISM; UBIQUITIN LIGASES; ENZYME-ACTIVITIES; BODY-COMPOSITION; PROTEIN; TROUT; INSULIN; ADIPONECTIN;
D O I
10.1186/1742-9994-6-18
中图分类号
Q95 [动物学];
学科分类号
071002 [动物学];
摘要
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.
引用
收藏
页数:13
相关论文
共 78 条
[11]
BONE Q, 1978, FISH B-NOAA, V76, P691
[12]
BOSS GR, 1985, J BIOL CHEM, V260, P6054
[13]
The cellular fate of glucose and its relevance in type 2 diabetes [J].
Bouché, C ;
Serdy, S ;
Kahn, CR ;
Goldfine, AB .
ENDOCRINE REVIEWS, 2004, 25 (05) :807-830
[14]
Switching to fast growth: the insulin-like growth factor (IGF) system in skeletal muscle of Atlantic salmon [J].
Bower, Neil I. ;
Li, Xuejun ;
Taylor, Richard ;
Johnston, Ian A. .
JOURNAL OF EXPERIMENTAL BIOLOGY, 2008, 211 (24) :3859-3870
[16]
The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments [J].
Bustin, Stephen A. ;
Benes, Vladimir ;
Garson, Jeremy A. ;
Hellemans, Jan ;
Huggett, Jim ;
Kubista, Mikael ;
Mueller, Reinhold ;
Nolan, Tania ;
Pfaffl, Michael W. ;
Shipley, Gregory L. ;
Vandesompele, Jo ;
Wittwer, Carl T. .
CLINICAL CHEMISTRY, 2009, 55 (04) :611-622
[17]
Effect of refeeding on IGFI, IGFII, IGF receptors, FGF2, FGF6, and myostatin mRNA expression in rainbow trout myotomal muscle [J].
Chauvigné, F ;
Gabillard, JC ;
Weil, C ;
Rescan, PY .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2003, 132 (02) :209-215
[18]
The E3 ligase MuRF1 degrades myosin heavy chain protein in dexamethasone-treated skeletal muscle [J].
Clarke, Brian A. ;
Drujan, Doreen ;
Willis, Monte S. ;
Murphy, Leon O. ;
Corpina, Richard A. ;
Burova, Elena ;
Rakhilin, Sergey V. ;
Stitt, Trevor N. ;
Patterson, Cam ;
Latres, Esther ;
Glass, David J. .
CELL METABOLISM, 2007, 6 (05) :376-385
[19]
Cyclic AMP signaling and gene regulation [J].
Daniel, PB ;
Walker, WH ;
Habener, JF .
ANNUAL REVIEW OF NUTRITION, 1998, 18 :353-383
[20]
Open source clustering software [J].
de Hoon, MJL ;
Imoto, S ;
Nolan, J ;
Miyano, S .
BIOINFORMATICS, 2004, 20 (09) :1453-1454