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首页> 外文期刊>Aquaculture Reports >Comparative transcriptome analysis reveals the potential influencing mechanism of dietary astaxanthin on growth and metabolism in Litopenaeus vannamei
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Comparative transcriptome analysis reveals the potential influencing mechanism of dietary astaxanthin on growth and metabolism in Litopenaeus vannamei

机译:比较转录组分析揭示了膳食虾青素对Litopenaeus Vannamei的生长和代谢的潜在影响机制

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The Pacific white shrimp ( Litopenaeus vannamei ), as one of the most valuable crustaceans, is widely distributed in China. Dietary astaxanthin has multiple functions in L. vannamei , such as promoting growth and antioxidant production. In the current study, shrimps were fed a diet which was supplemented with 0, 50, or 100 ppm astaxanthin for 4 weeks, and the specific growth rate (SGR) and weight gain were significantly greater in treatment groups compared to control group. We performed the transcriptome analysis of hepatopancreas of L. vannamei and detected 14,336, 14,780, and 14,400 genes, respectively. 598 and 285 genes were significant differentially expressed compared with the control group, under supplementation with 50 and 100 ppm astaxanthin, respectively, of which 434 and 104 were up-regulated and 164 and 181 were down-regulated. Through the KEGG pathway analysis, we found that the significant differentially expressed genes were mainly enriched in metabolic-related pathways, such as metabolic pathway, pyruvate metabolism, and glycolysis/gluconeogenesis pathway. Twelve genes were chosen to validate the results of RNA-Seq by qRT-PCR. This study provides valuable information about the effect of astaxanthin on L. vannamei . The genes and pathways, which are identified in the current study, can help to reveal the molecular mechanism responsible for the effect of astaxanthin on metabolism.
机译:太平洋白虾(Litopenaeus Vannamei)是最有价值的甲壳类动物之一,广泛分布在中国。饮食虾青素在L.Vannamei中具有多种功能,例如促进生长和抗氧化生产。在目前的研究中,虾喂养饮食,其补充有0,50或100ppm虾青素4周,与对照组相比,治疗组的特定生长速率(SGR)和体重增加显着更大。我们分别进行了L.Vannamei的肝癌和检测到14,336,14,780和14,400个基因的转录组分析。与对照组相比,598和285基因与对照组相比,在补充有50和100ppm虾青蛋白的补充,其中434和104被上调,164和181被下调。通过Kegg途径分析,我们发现显着的差异表达基因主要富集在代谢相关的途径中,例如代谢途径,丙酮酸代谢和糖酵解/葡糖基因途径。选择12个基因以通过QRT-PCR验证RNA-SEQ的结果。本研究提供了有关虾青素对L. Vannamei的影响的有价值的信息。在目前的研究中鉴定的基因和途径可以有助于揭示负责虾青素对代谢作用的分子机制。

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