首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Long-chain polyunsaturated fatty acid synthesis in fish: Comparative analysis of Atlantic salmon (Salmo salar L.) and Atlantic cod (Gadus morhua L.) Δ6 fatty acyl desaturase gene promoters
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Long-chain polyunsaturated fatty acid synthesis in fish: Comparative analysis of Atlantic salmon (Salmo salar L.) and Atlantic cod (Gadus morhua L.) Δ6 fatty acyl desaturase gene promoters

机译:鱼中长链多不饱和脂肪酸的合成:大西洋鲑(Salmo salar L.)和大西洋鳕(Gadus morhua L.)Δ6脂肪酰基去饱和酶基因启动子的比较分析

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摘要

Fish vary in the ability to biosynthesise n-3 long-chain polyunsaturated fatty acids (LC-PUFA), with marine fish such as cod being inefficient in comparison to freshwater and salmonid fish. We investigated differences in the gene promoters of Δ6 fatty acyl desaturase (Δ6 FAD), a critical enzyme in LC-PUFA biosynthesis, in cod and salmon. Progressive deletions and targeted mutations of the promoters were tested for activity in a transfected Atlantic salmon (AS) cell line under low or high LC-PUFA treatment, and regions sufficient to direct transcription were identified. Comparison of these regions with sequences of corresponding regions of Δ6 FAD genes from mammals, amphibians and fish indicated a remarkable conservation of binding sites for SREBPs and NF-Y. In addition to these sites, a site was identified in salmon with similarity to that recognised by Sp1 transcription factor, and which was required for full expression of the salmon Δ6 FAD gene. The cod promoter was less active and lacked the Sp1 site. Eicosapentaenoic acid suppressed LC-PUFA synthesis in AS cells and also suppressed activity of the salmon Δ6 FAD promoter although this activity was likely mediated through sites other than Sp1, possibly similar to those recognised by NF-Y and SREBP transcription factors.
机译:鱼的生物合成n-3长链多不饱和脂肪酸(LC-PUFA)的能力各不相同,与鳕鱼等海水鱼相比,淡水和鲑鱼鱼效率低。我们在鳕鱼和鲑鱼中研究了LC-PUFA生物合成中的关键酶Δ6脂肪酰基去饱和酶(Δ6FAD)的基因启动子的差异。在低或高LC-PUFA处理下,在转染的大西洋鲑鱼(AS)细胞系中测试了启动子的进行性缺失和靶向突变的活性,并鉴定出足以指导转录的区域。将这些区域与来自哺乳动物,两栖动物和鱼类的Δ6FAD基因的相应区域的序列进行比较表明,SREBP和NF-Y的结合位点显着保守。除了这些位点外,在鲑鱼中还发现了一个与Sp1转录因子识别的相似的位点,这是鲑鱼Δ6FAD基因完整表达所必需的。鳕鱼启动子活性较低,缺少Sp1位点。二十碳五烯酸抑制了AS细胞中LC-PUFA的合成,并且还抑制了鲑鱼Δ6FAD启动子的活性,尽管这种活性可能是通过Sp1以外的位点介导的,可能与NF-Y和SREBP转录因子识别的位点相似。

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