水产学杂志 ›› 2015, Vol. 28 ›› Issue (1): 11-17.

• 研究论文 • 上一篇    下一篇

镜鲤△6脂肪酸脱氢酶CDNA的克隆与表达

利用RT-PCR和RACE方法克隆得到了镜鲤Cyprinus carpio肝脏中高不饱和脂肪酸(HUFA)合成代谢的脂肪酸去饱和酶(△6FAD)基因cDNA全序列。结果表明:镜鲤△6FAD基因cDNA全长为1 446bp,开放阅读框(ORF)为1 332bp,编码444个氨基酸。编码的蛋白序列包含FAD全部特征结构区,包括1个细胞色素b5结构域、2个跨膜区和3个组氨酸簇,与其他鱼类的Δ6FAD氨基酸序列具有69.0%~92.0%的同源性。系统树分析显示:与斑马鱼Danio rerio的亲缘关系最近。实时荧光定量PCR(RT-qPCR)检测发现:脂肪酸延长酶基因在镜鲤肝脏中表达量最高,背部肌次之,在血液中表达最低。本研究结果为进一步研究镜鲤HUFA的合成途径及调控机理提供了基础资料。   

  1. 1.中国水产科学研究院黑龙江水产研究所,黑龙江 哈尔滨 150070;2.大连海洋大学水产与生命学院,辽宁 大连 116023
  • 出版日期:2015-02-15 发布日期:2015-04-21

  • Online:2015-02-15 Published:2015-04-21

摘要: 利用RT-PCR和RACE方法克隆得到了镜鲤Cyprinus carpio肝脏中高不饱和脂肪酸(HUFA)合成代谢的脂肪酸去饱和酶(△6FAD)基因cDNA全序列。结果表明:镜鲤△6FAD基因cDNA全长为1 446bp,开放阅读框(ORF)为1 332bp,编码444个氨基酸。编码的蛋白序列包含FAD全部特征结构区,包括1个细胞色素b5结构域、2个跨膜区和3个组氨酸簇,与其他鱼类的Δ6FAD氨基酸序列具有69.0%~92.0%的同源性。系统树分析显示:与斑马鱼Danio rerio的亲缘关系最近。实时荧光定量PCR(RT-qPCR)检测发现:脂肪酸延长酶基因在镜鲤肝脏中表达量最高,背部肌次之,在血液中表达最低。本研究结果为进一步研究镜鲤HUFA的合成途径及调控机理提供了基础资料。

关键词: △6脂肪酸脱氢酶, 镜鲤, 基因克隆, 表达分析

Abstract: The full-length Δ6FAD cDNA of mirror carp (Cyprinus carpio) was cloned by reverse transcript PCR (RT-PCR) and rapid amplification of cDNA ends (RACE) to study the regulatory role of Δ6 fatty acid desaturase in the biosynthesis of highly unsaturated fatty acid (HUFA). The cDNA for Δ6FAD gene was 1 446bp in full length including an ORF of 1 332 bp encoding a peptide with 444 amino acids (accession no.KJ576791). The protein sequence contained all the characteristics of microsomal fatty acid desaturases, including 3 histidine boxes, 2 transmembrane regions,and a cytochrome b5 domain.The protein sequence was characterized by microsomal fatty acid elongases and sharing 69% ~92.0% sequence identity with the Δ6 desaturase gene in other fish. The phylogenetic tree showed that it clustered closely into freshwater fishes. The expression of the enzyme gene in different tissues of mirror carp was detected by real-time quantity PCR (RT-qPCR), the maximum in the heptopancreas, followed by muscle, and the minimum in blood. There was higher expression level of Δ6FAD in liver than in other tissues, Indicating that heptopancreas is the main tissue of HUFA biosynthetic mechanism, with the minimal expression level of Δ6FAD in blood. The findings will be helpful for clarifying the HUFA biosynthetic mechanism in mirror carp and for the development of method in enhancing such ability.