Dataset Information

Estimation of genetic parameters for growth and carcass traits in turbot (Scophthalmus maximus).

ABSTRACT: Information on phenotypic and genetic (co)variance for production traits in turbot is required to improve breeding programs. So far, information on morphometric growth traits is sparse and completely lacking on quality carcass traits like fillet weight or fillet yield for turbot. As part of a long-term study we explored the phenotypic and genetic (co)variance of 16 biometrical and carcass traits of three different European turbot strains. Fish were reared under commercial grow-out conditions, including size grading. We used molecular relatedness (MR) methods based on genotyping with 96 microsatellite markers and animal models. We included an adapted condition factor for Pleuronectiformes (FCI PLN ) and average daily weight gain (ADG) between the ages of 300 and 500?d post-hatch (dph) for their potential correlation with body weight at harvest. Heritability estimates for all traits were low to medium (0.04-0.29) when strains were jointly analyzed. Separate analysis of strains yielded higher heritability estimates (0.12-0.43). Genetic correlations between weight-related traits were highly positive (0.70-0.99), while runs with yield and ratio traits often resulted in unreliable estimates of genetic correlation due to high standard errors. Body weight ( h2=0.19 ), fillet yield ( h2=0.1 5), and dressing percentage ( h2=0.17 ) are particularly promising selection traits for turbot breeding.

SUBMITTER: Schlicht K

PROVIDER: S-EPMC6852839 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Estimation of genetic parameters for growth and carcass traits in turbot (<i>Scophthalmus maximus</i>).

Schlicht Kristina K Krattenmacher Nina N Lugert Vincent V Schulz Carsten C Thaller Georg G Tetens Jens J

Archives animal breeding 20190506 1

Information on phenotypic and genetic (co)variance for production traits in turbot is required to improve breeding programs. So far, information on morphometric growth traits is sparse and completely lacking on quality carcass traits like fillet weight or fillet yield for turbot. As part of a long-term study we explored the phenotypic and genetic (co)variance of 16 biometrical and carcass traits of three different European turbot strains. Fish were reared under commercial grow-out conditions, in ...[more]

PMID: 31807637

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Project description:In mammals, forkhead box O3 (foxo3) plays important roles in liver immune system. The foxo3 can regulate cell cycle, DNA repair, hypoxia, apoptosis and so on. However, as such an important transcription factor, few studies on foxo3 in fish have been reported. The present study characterized the foxo3 in turbot (Scophthalmus maximus L.). Lipopolysaccharide (LPS) incubated in vitro (hepatocytes) and injected in vivo (turbot liver) were used to construct inflammatory models. The foxo3 was interfered and overexpressed to investigate its functions in liver inflammation. The open reading frame (ORF) of foxo3 was 1998 bp (base pair), encoding 665 amino acids. Sequence analysis showed that foxo3 of turbot was highly homologous to other fishes. Tissue distribution analysis revealed that the highest expression of foxo3 was in muscle. Immunofluorescence result showed that foxo3 was expressed in cytoplasm and nucleus. Knockdown of foxo3 significantly increased mRNA levels of tumor necrosis factor-α (tnf-α), interleukin-1β (il-1β), interleukin-6 (il-6), myeloid-differentiation factor 88 (myd88), cd83, toll-like receptor 2 (tlr-2) and protein level of c-Jun N-terminal kinase (JNK) in sifoxo3 + LPS (siRNA of foxo3+ LPS) group compared with NC + LPS (negative control + LPS) group in turbot hepatocytes. Overexpressed foxo3 significantly decreased mRNA levels of tnf-α, il-6, nuclear transcription factor-kappa B (nf-κb), cd83, tlr-2 and the protein level of JNK in vitro. In vivo analysis, foxo3 knockdown significantly increased levels of GOT in serum after LPS injection compared with NC+LPS group. Overexpressed foxo3 significantly decreased levels of GPT and GOT in pcDNA3.1-foxo3+LPS group compared with pcDNA3.1+LPS group in vivo. Foxo3 knockdown significantly increased mRNA levels of tnf-α, il-1β, il-6, nf-κb, myd88 and protein level of JNK in vivo in sifoxo3+LPS group compared with NC+LPS group in turbot liver. Overexpressed foxo3 significantly decreased mRNA levels of il-1β, il-6, myd88, cd83, jnk and protein level of JNK in pcDNA3.1-foxo3+LPS group compared with pcDNA3.1+LPS group in turbot liver. The results indicated that foxo3 might modulate LPS-activated hepatic inflammation in turbot by decreasing the proinflammatory cytokines, the levels of GOT and GPT as well as activating JNK/caspase-3 and tlr-2/myd88/nf-κb pathways. Taken together, these findings indicated that FoxO3 may play important roles in liver immune responses to LPS in turbot and the research of FoxO3 in liver immunity enriches the studies on immune regulation, and provides theoretical basis and molecular targets for solving liver inflammation and liver injury in fish.

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Dataset Information

Estimation of genetic parameters for growth and carcass traits in turbot (Scophthalmus maximus).

Publications

Estimation of genetic parameters for growth and carcass traits in turbot (<i>Scophthalmus maximus</i>).

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