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酿酒酵母翻译延伸因子3的序列分析。

Sequence analysis of the translational elongation factor 3 from Saccharomyces cerevisiae.

作者信息

Qin S L, Xie A G, Bonato M C, McLaughlin C S

机构信息

Department of Biological Chemistry, University of California, Irvine 92717.

出版信息

J Biol Chem. 1990 Feb 5;265(4):1903-12.

PMID:2404974
Abstract

The gene YEF-3 encoding the elongation factor for protein synthesis in Saccharomyces cerevisiae is an essential gene as shown by one-step gene disruption and is located on chromosome XII as determined by orthogonal field alternation gel electrophoresis. The nucleotide sequence of the gene was determined from a sequential series of subclones generated from the YEF-3 gene cloned into bacteriophage M13. The HOMOL1 sequence and the RPG box, which are considered to be enhancer elements involved in coordinate regulation of transcription of the genes coding for yeast ribosomal proteins and protein synthesis factors, are found in the 5'-flanking region of the gene. A dyad symmetry that enables hairpin loop formation in the DNA molecule is found in the 3'-terminal at the termination site of transcription. An open reading frame of 3132 nucleotides codes for a deduced protein of 115,860 Da. A striking feature of the elongation factor 3 deduced polypeptide is the internal repeat of a region with approximately 200 amino acids which includes an ATP-binding site and shares similarity with some transport and drug-resistant proteins. Another characteristic is the presence of a highly charged C-terminal region composed of three basic polylysine blocks, suggesting interaction with RNA. The sequence supports the hypothesis that YEF-3 encodes a protein synthesis factor and suggests that its main role may be to transduce nucleoside triphosphate energy into mechanical energy for translocation during translation.

摘要

编码酿酒酵母蛋白质合成延伸因子的基因YEF-3是一个必需基因,一步基因敲除实验证明了这一点,正交交变电场凝胶电泳确定该基因位于第十二号染色体上。该基因的核苷酸序列是从克隆到噬菌体M13中的YEF-3基因产生的一系列连续亚克隆中测定的。在该基因的5'侧翼区域发现了HOMOL1序列和RPG框,它们被认为是参与酵母核糖体蛋白和蛋白质合成因子编码基因转录协同调控的增强子元件。在转录终止位点的3'末端发现了一个能使DNA分子形成发夹环的二元对称结构。一个3132个核苷酸的开放阅读框编码一个推导分子量为115,860 Da的蛋白质。延伸因子3推导多肽的一个显著特征是一个约200个氨基酸区域的内部重复,该区域包括一个ATP结合位点,并且与一些转运蛋白和耐药蛋白具有相似性。另一个特征是存在由三个碱性多聚赖氨酸块组成的高度带电的C末端区域,提示其与RNA相互作用。该序列支持YEF-3编码一种蛋白质合成因子的假说,并表明其主要作用可能是在翻译过程中将核苷三磷酸能量转化为用于转位的机械能。

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