Abstract

BackgroundSexual maturation causes loss of fish muscle mass and deterioration of fillet quality attributes that prevent market success. We recently showed that fillet yield and flesh quality recover in female trout after spawning. To gain insight into the molecular mechanisms regulating flesh quality recovery, we used an Agilent-based microarray platform to conduct a large-scale time course analysis of gene expression in female trout white muscle from spawning to 33 weeks post-spawning.ResultsIn sharp contrast to the situation at spawning, muscle transcriptome of female trout at 33 weeks after spawning was highly similar to that of female trout of the same cohort that did not spawn, which is consistent with the post-spawning flesh quality recovery. Large-scale time course analysis of gene expression in trout muscle during flesh quality recovery following spawning led to the identification of approximately 3340 unique differentially expressed genes that segregated into four major clusters with distinct temporal expression profiles and functional categories. The first cluster contained approximately 1350 genes with high expression at spawning and downregulation after spawning and was enriched with genes linked to mitochondrial ATP synthesis, fatty acid catabolism and proteolysis. A second cluster of approximately 540 genes with transient upregulation 2 to 8 weeks after spawning was enriched with genes involved in transcription, RNA processing, translation, ribosome biogenesis and protein folding. A third cluster containing approximately 300 genes upregulated 4 to 13 weeks after spawning was enriched with genes encoding ribosomal subunits or regulating protein folding. Finally, a fourth cluster that contained approximately 940 genes with upregulation 8 to 24 weeks after spawning, was dominated by genes encoding myofibrillar proteins and extracellular matrix components and genes involved in glycolysis.ConclusionOverall, our study indicates that white muscle tissue restoration and flesh quality recovery after spawning are associated with transcriptional changes promoting anaerobic ATP production, muscle fibre hypertrophic growth and extracellular matrix remodelling. The generation of the first database of genes associated with post-spawning muscle recovery may provide insights into the molecular and cellular mechanisms controlling muscle yield and fillet quality in fish and provide a useful list of potential genetic markers for these traits.

Highlights

  • Sexual maturation causes loss of fish muscle mass and deterioration of fillet quality attributes that prevent market success

  • To gain insight into the transcriptomic changes associated with flesh quality restoration after spawning we performed microarray hybridisations using RNA extracted from the muscle tissues of mature female trout sampled at 0, 2, 4, 8, 13, 16, 24, and 33 weeks after spawning (PS0, PS2, PS4, PS8, PS13, PS16, PS24, and PS33) and from the muscle tissues of immature female trout

  • We found that the muscle transcriptome of trout that had just spawned (PS0) was clearly different from that of control trout (C0), as revealed by the identification of approximately 4700 unique differentially expressed genes (DEGs) between PS0 and C0

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Summary

Introduction

Sexual maturation causes loss of fish muscle mass and deterioration of fillet quality attributes that prevent market success. We recently showed that fillet yield and flesh quality recover in female trout after spawning. Muscle growth and fillet quality are important traits that impact the profitability of the fish breeding industry. Fertile diploid female trout those that are farmed for egg production, exhibit low flesh quality and a decrease in fillet yield around the spawning period and are not suitable for the market. Flesh deterioration at spawning is due in large part to muscle atrophy associated with protein catabolism which is exacerbated in the muscle tissue of maturing female trout to provide the energy and nutrients necessary for egg development [2]. Some of the lipids mobilized during sexual maturation originate from muscle store [3,4,5]

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