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来自溶组织内阿米巴的一种异常延伸因子-1α cDNA的克隆与特性分析

Cloning and characterization of an unusual elongation factor-1 alpha cDNA from Entamoeba histolytica.

作者信息

De Meester F, Bracha R, Huber M, Keren Z, Rozenblatt S, Mirelman D

机构信息

MacArthur Center for Molecular Biology of Parasitic Diseases, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Mol Biochem Parasitol. 1991 Jan;44(1):23-32. doi: 10.1016/0166-6851(91)90217-t.

Abstract

The coding sequence deduced from two overlapping cDNA inserts obtained from a pathogenic strain of Entamoeba histolytica revealed a striking homology (greater than 85%) with elongation factor EF-1 alpha from Saccharomyces cerevisiae and Artemia salina. The deduced amino acid sequence predicted a size of 49 kDa, and antibodies raised against the S. cerevisiae EF-1 alpha cross-reacted with an amoebic protein of similar size (45-47 kDa). Sequence analysis of the cDNA revealed that the 5' untranslated region contained a stretch of 190 nucleotides which was perfectly complementary to a segment of the 3' terminal coding region situated 1015 bases downstream of the methionine initiation codon. Electron microscopy of self-renatured cDNA confirmed the potential of such molecules to form a stem-loop secondary structure. The presence of the complementary sequences was confirmed at the genomic level by sequence analysis of polymerase chain reaction-amplified segments which span both the 3' and 5' terminal complementary regions. Comparison of the deduced amino acid sequence of E. histolytica EF-1 alpha with Ef-Tu from Escherichia coli and EF-1 alpha from different sources, suggested that the major functional domains of the protein are located within the loop structure.

摘要

从溶组织内阿米巴致病菌株获得的两个重叠cDNA插入片段推导的编码序列,与酿酒酵母和卤虫的延伸因子EF-1α显示出显著的同源性(大于85%)。推导的氨基酸序列预测大小为49 kDa,针对酿酒酵母EF-1α产生的抗体与大小相似(45-47 kDa)的阿米巴蛋白发生交叉反应。cDNA的序列分析表明,5'非翻译区包含一段190个核苷酸的序列,该序列与位于甲硫氨酸起始密码子下游1015个碱基处的3'末端编码区的一段序列完全互补。对自身复性的cDNA进行电子显微镜观察证实了此类分子形成茎环二级结构的可能性。通过对跨越3'和5'末端互补区域的聚合酶链反应扩增片段进行序列分析,在基因组水平上证实了互补序列的存在。将溶组织内阿米巴EF-1α推导的氨基酸序列与大肠杆菌的Ef-Tu以及不同来源的EF-1α进行比较,表明该蛋白的主要功能域位于环结构内。

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