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Characteristics of fads2 gene expression and putative promoter in European sea bass (Dicentrarchus labrax): Comparison with salmonid species and analysis of CpG methylation

机译:欧洲鲈鱼(Dicentrarchus labrax)中fads2基因表达和推定启动子的特征:与鲑鱼种的比较和CpG甲基化分析

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Marine fish species exhibit low capacity to biosynthesise highly unsaturated fatty acid (HUFA) in comparison to strict freshwater and anadromous species. It is admitted that the Delta(6) desaturase (FADS2) is a key enzyme in the HUFA biosynthetic pathway. We investigated by quantitative PCR the relative amounts of FADS2 mRNA in European sea bass (Dicentrarchus labrax) in comparison with a salmonid species, the rainbow trout (Oncorhynchus mykiss L.). The analysis of the expression data was performed regarding the difference of the characteristics of a critical fragment of the fads2 gene promoter between sea bass and Atlantic salmon. The lower level of fads2 gene expression observed in sea bass suggested that fads2 gene putative promoter, which exhibited an E-box like Sterol Regulatory Element (SRE) site but lacked a Sp1 site, is less active in this marine species. The cytosine methylation of CpG sites in the putative promoter region including E-box like SRE and NF-Y binding sites of sea bass fads2 gene was also investigated following a nutritional conditioning of larvae. However, no significant difference of CpG methylation could be found for any of the 28 CpGs analysed between larvae fed diet with high or low HUFA contents. In conclusion, the present data revealed lower constitutive expression of the fads2 gene possibly related to different characteristics of gene promoter in sea bass in comparison with salmonid species, and indicated that long-term conditioning of fads2 gene expression did not influence the methylation of the gene promoter at potential SRE binding site.
机译:与严格的淡水和淡水鱼类相比,海水鱼类生物合成高不饱和脂肪酸(HUFA)的能力较低。公认的是,Delta(6)去饱和酶(FADS2)是HUFA生物合成途径中的关键酶。我们通过定量PCR调查了欧洲鲈鱼(Dicentrarchus labrax)与鲑鱼物种虹鳟(Oncorhynchus mykiss L.)相比,FADS2 mRNA的相对含量。关于鲈鱼和大西洋鲑鱼之间的fads2基因启动子的关键片段的特征的差异,进行了表达数据的分析。在鲈鱼中观察到的fads2基因表达水平较低,这表明fads2基因推定的启动子在这种海洋物种中的活性较低,该启动子表现出类似Sterol调控元件(SRE)位点的E-box,但缺少Sp1位点。在幼虫的营养条件下,还研究了推定的启动子区域(包括E-box样的SRE和海鲈fads2基因的NF-Y结合位点)中CpG位点的胞嘧啶甲基化。但是,在HUFA含量高或低的幼虫饲喂日粮之间分析的28种CpG中,没有发现CpG甲基化有显着差异。总之,目前的数据表明,与鲑鱼种类相比,fads2基因的组成型表达可能与鲈鱼中基因启动子的不同特征有关,并且表明fads2基因表达的长期调节不会影响该基因的甲基化。在潜在的SRE结合位点的启动子。

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