Tocher Douglas R, Zheng Xiaozhong, Schlechtriem Christian, Hastings Nicola, Dick James R, Teale Alan J
Institute of Aquaculture, University of Stirling, Stirling FK9 4LA, Scotland, United Kingdom.
Lipids. 2006 Nov;41(11):1003-16. doi: 10.1007/s11745-006-5051-4.
This study reports the cloning, functional characterization, tissue expression, and nutritional regulation of a delta6 fatty acyl desaturase of Atlantic cod (Gadus morhua). PCR primers were designed based on the sequences of conserved motifs in available fish desaturases and used to isolate a cDNA fragment from cod liver, with full-length cDNA obtained by rapid amplification of cDNA ends. The cDNA for the putative desaturase was shown to comprise 1980 bp, including a 261-bp 5'-UTR, a 375-bp 3'-UTR, and an ORF of 1344 bp that specified a protein of 447 amino acids. The protein sequence included three histidine boxes, two transmembrane regions, and an N-terminal cytochrome b5 domain containing the heme-binding motif HPGG, all characteristic of microsomal fatty acyl desaturases. The cDNA displayed delta6 desaturase activity in a yeast expression system. Quantitative real-time PCR assay of gene expression in cod showed that the delta6 desaturase gene was expressed highly in brain, to a slightly lesser extent in liver, kidney, intestine, red muscle, and gill, and at much lower levels in white muscle, spleen, and heart. The expression of the delta6 desaturase gene did not appear to be under significant nutritional regulation, with levels in liver and intestine being barely altered in fish fed a vegetable oil blend, in comparison with levels in fish fed fish oil. This was reflected in enzyme activity, as hepatocytes or enterocytes showed very little highly unsaturated FA biosynthesis activity irrespective of diet. Further studies are required to determine why the delta6 desaturase appears to be barely functional in cod under the conditions tested.
本研究报告了大西洋鳕鱼(Gadus morhua)δ6脂肪酸去饱和酶的克隆、功能特性、组织表达及营养调控。基于现有鱼类去饱和酶保守基序的序列设计了PCR引物,并用于从鳕鱼肝脏中分离出一个cDNA片段,通过cDNA末端快速扩增获得全长cDNA。推测的去饱和酶的cDNA显示为1980 bp,包括一个261 bp的5'-UTR、一个375 bp的3'-UTR和一个1344 bp的开放阅读框,该开放阅读框编码一个447个氨基酸的蛋白质。蛋白质序列包括三个组氨酸盒、两个跨膜区域以及一个含有血红素结合基序HPGG的N端细胞色素b5结构域,这些都是微粒体脂肪酸去饱和酶的特征。该cDNA在酵母表达系统中显示出δ6去饱和酶活性。对鳕鱼基因表达的定量实时PCR分析表明,δ6去饱和酶基因在脑中高表达,在肝脏、肾脏、肠道、红肌和鳃中的表达程度稍低,而在白肌、脾脏和心脏中的表达水平则低得多。δ6去饱和酶基因的表达似乎不受显著的营养调控,与喂食鱼油的鱼相比,喂食植物油混合物的鱼肝脏和肠道中的水平几乎没有变化。这在酶活性中得到体现,因为无论饮食如何,肝细胞或肠细胞显示出非常少的高度不饱和脂肪酸生物合成活性。需要进一步研究以确定为什么在测试条件下δ6去饱和酶在鳕鱼中似乎几乎没有功能。