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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Molecular cloning and expression analysis on LPL of Coilia nasus
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Molecular cloning and expression analysis on LPL of Coilia nasus

机译:Co虫LPL的分子克隆和表达分析

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Coilia nasus is one important commercial anadromous species which mainly distributed in the Yangtze River in China. At present, it has been on the "National Key Protective Species List" because of its severe resource damage. Lipid metabolism is very important during its long-distance migration. To make further research on lipid metabolism of C. nasus, we cloned lipoprotein lipase gene with homologous cloning method. A full-length cDNA of LPL of C nasus was cloned from liver which covered 3537 bp with a 1519 bp open reading frame encoding 505 deduced amino acids whose molecular mass was 57.5 kDa and theoretical isoelectric point was 7.58. The deduced amino acids had high similarity with the reported LPL sequence of other species. It had typical conserved domain of LPL protein containing catalytic triad, N-linked glycosylation sites and conserved heparin-binding site, etc. We adopted quantitative real-time RT-PCR method to detect the mRNA expression of LPL of C nasus in ten tissues including mesenteric adipose, liver, muscle, stomach, spleen, heart, head kidney, trunk kidney, gill and brain with beta-actin as internal reference. LPL expressed in all the detected tissues. The highest expression was in mesenteric adipose, and followed by liver, muscle, stomach. Lipid expressed lowly in spleen, heart, head kidney, trunk kidney, gill and brain. The research on the cloning and differential expression of LPL of C. nasus will lay foundation for further research on lipid metabolism of C. nasus. (C) 2016 Elsevier B.V. All rights reserved.
机译:虫是一种重要的商业性无翅物种,主要分布在中国长江中。由于其严重的资源破坏,目前已列入“国家重点保护物种名录”。脂质代谢在其长距离迁移过程中非常重要。为了进一步研究鼻鱼的脂质代谢,我们采用同源克隆的方法克隆了脂蛋白脂肪酶基因。从肝脏克隆了鼻虫LPL的全长cDNA,其全长3537 bp,具有1519 bp的开放阅读框,编码505个推导的氨基酸,分子量为57.5 kDa,理论等电点为7.58。推导的氨基酸与报道的其他物种的LPL序列具有高度相似性。它具有典型的LPL蛋白保守结构域,该结构域包含催化三联体,N-连接的糖基化位点和保守的肝素结合位点等。我们采用定量实时RT-PCR方法检测了10个组织中C鼻的LPL mRNA表达。肠系膜脂肪,肝脏,肌肉,胃,脾脏,心脏,头部肾脏,躯干肾脏,g和大脑,以β-肌动蛋白作为内部参照。 LPL在所有检测到的组织中表达。表达最高的是肠系膜脂肪,其次是肝,肌肉,胃。脂质在脾脏,心脏,头肾,躯干肾,g和脑中表达较低。鼻虫LPL的克隆和差异表达的研究将为进一步研究鼻虫脂质代谢奠定基础。 (C)2016 Elsevier B.V.保留所有权利。

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