Suppr超能文献

克氏锥虫TcRjl基因座的特征分析及其转录本分析

Characterization of Trypanosoma cruzi TcRjl locus and analysis of its transcript.

作者信息

Nepomuceno-Silva J L, De Melo L D B, Mendonça S M, Paixão J C, Lopes U G

机构信息

Laboratório de Parasitologia Molecular, Instituto de Biofisica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, RJ, 21949-900, Brazil.

出版信息

Parasitology. 2004 Sep;129(Pt 3):325-33. doi: 10.1017/s0031182004005621.

Abstract

RJLs represent a recently described family of the Ras-related GTP-binding proteins. The Trypanosoma cruzi orthologue, TeRjl, was isolated and its locus was characterized in a region of almost 5 kb. Its 660 bp orf, predicting a protein of 24.13 kDa, is present as a single copy gene in T. cruzi I lineage, and from 1-2 copies in T. cruzi II lineage. TcRjl shares 73% aa sequence similarity with its closest identified orthologue, T. brucei TbRjl. RT-PCR experiments revealed that TcRjl is transcribed in mRNA in the 3 main life forms of the parasite, while Northern hybridization demonstrated that TcRjl is transcribed in T. cruzi epimastigotes as at least 2 transcripts, one of around 950 nt and the other of 1500 nt. Splice-leader addition was mapped to a single site at -69 bp upstream of TcRjl orf indicating that the two mRNA types may derive in differences at the 3' of TcRjl mRNA. TcRjl locus presents considerable synteny with Rjl loci from Trypanosoma brucei and Leishmania major as available from their respective genome projects.

摘要

RJLs代表最近描述的一类与Ras相关的GTP结合蛋白。分离出了克氏锥虫的直系同源物TeRjl,并对其在一个近5 kb的区域内的基因座进行了表征。其660 bp的开放阅读框预测编码一个24.13 kDa的蛋白质,在克氏锥虫I系中作为单拷贝基因存在,在克氏锥虫II系中有1至2个拷贝。TcRjl与其最接近的已鉴定直系同源物布氏锥虫TbRjl的氨基酸序列相似度为73%。逆转录聚合酶链反应实验表明,TcRjl在该寄生虫的3种主要生命形式中均转录为信使核糖核酸,而Northern杂交显示,TcRjl在克氏锥虫前鞭毛体中转录为至少2种转录本,一种约950 nt,另一种为1500 nt。剪接前导序列添加被定位到TcRjl开放阅读框上游-69 bp处的单个位点,这表明这两种信使核糖核酸类型可能源于TcRjl信使核糖核酸3'端的差异。根据来自布氏锥虫和硕大利什曼原虫各自基因组计划的信息,TcRjl基因座与它们的Rjl基因座具有相当程度的同线性。

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