双齿围沙蚕Cu/Zn-SOD cDNA基因的克隆及序列分析  

Cloning and sequence analysis of Cu /Zn- SOD cDNA from sandworm Perinereis aibuhitensis

作　　者：岳宗豪[1] 樊鑫[1] 赵欢[1] 任洪伟[1] 张旭峰[1] 周一兵[1] 

机构地区：[1]大连海洋大学辽宁省海洋生物资源恢复与生境修复重点实验室,辽宁大连116023

出　　处：《大连海洋大学学报》2014年第4期354-359,共6页Journal of Dalian Ocean University

基　　金：国家海洋公益性行业科研专项(201305002;201305043);国家海洋局重点实验室开放基金资助项目(201217);国家自然科学基金资助项目(41306138)

摘　　要：根据已知多毛类Alitta succinea铜锌超氧化物歧化酶(Cu/Zn-SOD)基因序列设计引物,利用同源克隆及RACE方法首次从双齿围沙蚕Perinereis aibuhitensis中克隆得到Cu/Zn-SOD基因全长cDNA序列。结果表明:双齿围沙蚕Cu/Zn-SOD基因cDNA全长870 bp,其中包括156 bp的5'端非编码区,261 bp 3'端非翻译区和453 bp开放阅读框,编码150个氨基酸;该蛋白序列具有典型的Cu2+和Zn2+结合位点,并具有两处Cu/Zn-SOD蛋白家族标签序列。通过生物信息学分析表明,该蛋白属于胞内Cu/Zn-SOD,理论相对分子质量为15 249 900,等电点为5.66,无信号肽和跨膜区,推测为亲水性蛋白。同源性分析表明,双齿围沙蚕Cu/Zn-SOD氨基酸序列与部分软体动物、鱼类和昆虫的Cu/Zn-SOD蛋白序列具有很高的相似性。该研究结果为后续研究Cu/Zn-SOD与环境污染物之间的剂量效应关系奠定了基础,为研究双齿围沙蚕机体的防御机制提供了基础资料。A full length cDNA of Cu/Zn-SOD was firstly cloned in sandworm Perinereis aibuhitensis by homology cloning and RACE techniques based on the partial copper-zinc superoxide dismutase （ Cu/Zn-SOD） gene from pol-ychaete Alitta succinea. The full length of the cDNA was found to be 870 bp including a 156 bp 5′untranslated re-gion,a 261 bp 3′untranslated region and 453 bp open reading frame encoding 150 amino acids. There were typical Cu2＋ and Zn2＋ binding sites as well as two Cu/Zn-SOD protein family tag sequences in the deduced protein which was within the intracellular Cu/Zn-SOD with relative molecular mass of 15 249 900 and the isoelectric point of 5. 66 by bioinformatic analysis. No signal peptide and transmembrane domain were observed in the deduced pro-tein, indicating that it belonged to the hydrophilic protein. Multiple sequences alignment analysis revealed that the deduced amino acids had high homology to the proteins of partial molluscs, fishes and insects. The findings will provide basis for research of dose-response between gene expression and environmental pollutants, and defense mechanism of the sandworm.

关 键 词：双齿围沙蚕 铜锌超氧化物歧化酶 生物信息学分析 同源性分析 

分 类 号：Q78[生物学—分子生物学] S917[农业科学—水产科学]