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溶组织内阿米巴α-微管蛋白编码基因的克隆、基因组结构及转录

Cloning, genomic organization and transcription of the Entamoeba histolytica alpha-tubulin-encoding gene.

作者信息

Sánchez M A, Peattie D A, Wirth D, Orozco E

机构信息

Department of Experimental Pathology, CINVESTAVI.P.N., Mexico, D.F., Mexico.

出版信息

Gene. 1994 Sep 2;146(2):239-44. doi: 10.1016/0378-1119(94)90299-2.

DOI:10.1016/0378-1119(94)90299-2
PMID:8076825
Abstract

We have isolated and characterized an Entamoeba histolytica alpha-tubulin (alpha Tub)-encoding gene (Eh alpha tub). A 700-bp DNA fragment was amplified by PCR using primers derived from consensus alpha- and beta-Tub amino acid (aa) sequences from different organisms and E. histolytica DNA as the template. These PCR fragments were used to screen both genomic DNA and cDNA libraries in order to isolate an Eh alpha tub structural gene. Two overlapping clones containing the complete alpha tub ORF (1392 bp) were isolated from the genome and cDNA libraries. The deduced aa sequence of Eh alpha Tub has 55.5, 50 and 52% identity to Plasmodium falciparum alpha Tub 2, Saccharomyces cerevisiae alpha Tub 2 and human alpha Tub, respectively. Interestingly, the predicted Eh alpha Tub protein lacks a poly-acidic motif at its C terminus which is involved in Tub polymerization and microtubule-associated protein binding in other organisms. This fact may indicate a difference in tubule assembly in this organism and could provide a potential key for the development of therapeutic agents. According to Southern blot experiments and the sequences of several clones, at least two non-adjacent copies of alpha tub are present in the E. histolytica genome. A 1.5-kb transcript corresponding to the alpha tub mRNA was detected in mRNA from asynchronous E. histolytica trophozoites.

摘要

我们已经分离并鉴定了一个编码溶组织内阿米巴α-微管蛋白(α Tub)的基因(Ehα tub)。使用从不同生物体的α-和β-微管蛋白氨基酸(aa)共有序列推导而来的引物以及溶组织内阿米巴DNA作为模板,通过PCR扩增出一个700 bp的DNA片段。这些PCR片段用于筛选基因组DNA文库和cDNA文库,以分离Ehα tub结构基因。从基因组文库和cDNA文库中分离出两个包含完整α tub开放阅读框(1392 bp)的重叠克隆。推导的Ehα Tub氨基酸序列与恶性疟原虫α Tub 2、酿酒酵母α Tub 2和人α Tub的同一性分别为55.5%、50%和52%。有趣的是,预测的Ehα Tub蛋白在其C末端缺乏一个多酸性基序,该基序在其他生物体中参与微管蛋白聚合和微管相关蛋白结合。这一事实可能表明该生物体中微管组装存在差异,并可能为治疗药物的开发提供潜在关键。根据Southern印迹实验和几个克隆的序列,溶组织内阿米巴基因组中至少存在两个不相邻的α tub拷贝。在来自异步生长的溶组织内阿米巴滋养体的mRNA中检测到一个与α tub mRNA相对应 的1.5 kb转录本。

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