Suppr超能文献

[八肋游仆虫rab基因家族一个新成员的克隆与序列分析]

[Cloning and sequence analysis of a novel member of the rab gene family from Euplotes octocarinatus].

作者信息

Li Ling-Yan, Chai Bao-Feng, Liang Ai-Hua, Sun Yong-Hua, Wang Wei

机构信息

Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Biotechnology, Shanxi University, Taiyuan 030006, China.

出版信息

Yi Chuan. 2006 Apr;28(4):437-42.

Abstract

Rab proteins belong to a subfamily of small GTP-binding proteins of the Ras superfamily, which play an important role in intracellular vesicular traffic. In this study, a rab gene was obtained from Euplotes octocarinatus by polymerase chain reaction (PCR) and RT-PCR. The rab gene from macronucleic DNA was 884 bp in length, including non-coding regions and telomeric sequences at both ends. The rab gene from micronuclear DNA (723 bp), lacking of internal eliminated sequences, was identical to rab gene from macronuclear DNA. RT-PCR showed that the opening reading frame of the rab gene was 663 bp long. The rab gene from macronuclear DNA contained an intron of 60 bp at the position from 153 bp to 212 bp of macronuclear DNA. The rab gene had two in-frame TGAs encoding for cysteine in Euplotes octocarinatus. The rab gene used TAG as stop codon, which was the first report in Euplotes octocarinatus. The result of BLAST in NCBI demonstrates that the Rab shares a homology of 49-52% at the amino acid level with Rab1 proteins from a number of other eukaryote, which suggesting that the Rab is a Rab1 homolog. The rab gene was therefore designated Eo-rab-1N (GenBank accession number: DQ105562). The evolution of Eo-rab-1N was analyzed using phylogenetic tree of amino acids sequences of Rab1 obtained from GenBank.

摘要

Rab蛋白属于Ras超家族中小GTP结合蛋白的一个亚家族,在细胞内囊泡运输中起重要作用。在本研究中,通过聚合酶链反应(PCR)和逆转录聚合酶链反应(RT-PCR)从八肋游仆虫中获得了一个rab基因。来自大核DNA的rab基因长度为884 bp,包括两端的非编码区和端粒序列。来自小核DNA的rab基因(723 bp),缺乏内部消除序列,与来自大核DNA的rab基因相同。RT-PCR显示rab基因的开放阅读框长663 bp。来自大核DNA的rab基因在大核DNA的153 bp至212 bp位置含有一个60 bp的内含子。在八肋游仆虫中,rab基因有两个编码半胱氨酸的框内TGA。rab基因使用TAG作为终止密码子,这在八肋游仆虫中是首次报道。NCBI中的BLAST结果表明,该Rab与许多其他真核生物的Rab1蛋白在氨基酸水平上具有49 - 52%的同源性,这表明该Rab是Rab1的同源物。因此,将该rab基因命名为Eo-rab-1N(GenBank登录号:DQ105562)。使用从GenBank获得的Rab1氨基酸序列的系统发育树分析了Eo-rab-1N的进化。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验