鳜凋亡相关基因的克隆与功能研究
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摘要
鳜(Siniperca chuatsi)是我国一种重要的淡水养殖鱼类,但是各种疾病的发生严重影响着其产量,免疫防治是控制疾病的重要而有效的途径。细胞凋亡是鱼类非特异性免疫调节的一个重要方面,本文对鳜凋亡相关基因进行了克隆鉴定及功能研究。
     通过构建SMART cDNA文库并结合RACE技术首次在鳜中克隆到三个凋亡相关基因,并采用PCR和Genome Walking的方法克隆这三个基因及其启动子区域。鳜肿瘤坏死因子相关的凋亡诱导配体(ScTRAIL)基因cDNA全长1359 bp,5′和3′非翻译区分别为112 bp和395 bp,开放阅读框包含852 bp,编码283 aa,基因全长9021 bp,含有6个外显子和5个内含子。启动子区域732 bp,缺乏典型的TATA或CAAT结构,但存在Oct-1、Sp-1、NF-1、RAP-1、C/EBPalp、NF-kappaB和AP-1等潜在的转录因子结合位点。
     鳜肿瘤坏死因子相关的凋亡诱导配体的诱骗受体(ScDcTRAILR)基因,cDNA全长2494 bp,5′和3′非编码区分别为106 bp和1326 bp,开放阅读框包含1062 bp,编码353 aa,基因全长10437 bp,含有10个外显子和9个内含子。启动子区域804 bp,缺乏典型的TATA框或CAAT盒,但有一些特异的转录因子结合位点,如C/EBPalp、Sp-1、Oct-1和GATA-1等。
     鳜Mst3和SOK1相关激酶(ScMASK)基因,cDNA全长1743 bp,5′和3′非编码区分别为161 bp和364 bp,开放阅读框包含1218 bp,编码405 aa,基因全长8561 bp,包含有9个外显子和8个内含子。启动子区域1526 bp,缺乏典型的TATA框或CAAT盒,存在Oct-1、Sp-1、NF-1、RAP-1、C/EBPalp、NF-kappaB和AP-1等潜在的转录因子结合位点。Southern blotting分析表明在鳜基因组中,ScTRAIL基因为单拷贝基因,在此基础上采用荧光定量PCR方法揭示ScDcTRAILR和ScMASK基因也是单拷贝基因。
     对三个基因转录和表达产物的器官组织分布进行了详细的分析。RT-PCR表明这三个基因在健康鳜组织中呈组成型表达,且三者具有不同的组织分布模式。分别构建ScTRAIL、ScDcTRAILR和ScMASK基因的原核表达质粒,通过原核表达、表达蛋白纯化、并制备多克隆抗体,对头肾、肾脏、肝脏、脾脏、肠、皮肤、心脏、脑、鳃和心
The mandarin fish Siniperca chuatsi is an important species in China’s aquaculture. The culture of the mandarin fish has been threatened seriously by many kinds of diseases. It is thus important and necessary to develop some effective methods for the control of diseases. The understanding of immune system in this fish will provide a base for such development. The present study aimed to clone some apoptosis-related genes for the mandarin fish, with their apoptotic function analyzed in cell lines.
     Three apoptosis related genes were cloned for the first time in the mandarin fish, i.e. TNF-related apoptosis-inducing ligand (TRAIL), a TRAIL decoy receptor (DcScTRAILR) and Mst3 and SOK1-related kinase (MASK) which are named as ScTRAIL, and ScDcTRAIL, and ScMASK. ScRAIL gene with the full-length cDNA of 1359 bp contains an open reading frame coding for a 283 aa protein; it’s full length genome has 9021 bp which contains six exons and five introns. The promoter region of ScTRAIL is 732 bp, which contains some putative transcription factor binding sites such as Oct-1, Sp-1, NF-1, RAP-1, C/EBPalp, NF-kappaB and AP-1; however, it lacks typical TATA or CAAT box. The ScDcTRAILR gene with the full-length cDNA of 2494 bp contains an open reading frame coding for a 353 aa protein; its full-length genome sequence is 10437 bp which contains ten exons and nine introns. The promoter region of ScDcTRAILR is 804 bp, which contains some putative transcription factor binding sites such as C/EBPalp、Sp-1、Oct-1 and GATA-1, but it lacks
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