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庚型肝炎病毒重叠基因中特征序列的检测及一个新重叠基因的预测

Detection of signature sequences in overlapping genes and prediction of a novel overlapping gene in hepatitis G virus.

作者信息

Pavesi A

机构信息

Department of Evolutionary and Functional Biology, University of Parma, Parco Area delle Scienze 11/A, I-43100 Parma, Italy.

出版信息

J Mol Evol. 2000 Mar;50(3):284-95. doi: 10.1007/s002399910033.

Abstract

In viruses an increased coding ability is provided by overlapping genes, in which two alternative open reading frames (ORFs) may be translated to yield two distinct proteins. The identification of signature sequences in overlapping genes is a topic of particular interest, since additional out-of-frame coding regions can be nested within known genes. In this work, a novel feature peculiar to overlapping coding regions is presented. It was detected by analysis of a sample set of 21 virus genomic sequences and consisted in the repeated occurrence of a cluster of basic amino acid residues, encoded by a frame, combined to a stretch of acidic residues, encoded by the corresponding overlapping frame. A computer scan of an additional set of virus sequences demonstrated that this feature is common to several other known overlapping ORFs and led to prediction of a novel overlapping gene in hepatitis G virus (HGV). The occurrence of a bifunctional coding region in HGV was also supported by its extremely lower rate of synonymous nucleotide substitutions compared to that observed in the other gene regions of the HGV genome. Analysis of the amino acid sequence that was deduced from the putative overlapping gene revealed a high content of basic residues and the presence of a nuclear targeting signal; these characteristics suggest that a core-like protein may be expressed by this novel ORF.

摘要

在病毒中,重叠基因可增强编码能力,即两个不同的开放阅读框(ORF)可被翻译产生两种不同的蛋白质。重叠基因中特征序列的识别是一个特别有趣的话题,因为额外的移码编码区域可能嵌套在已知基因内。在这项研究中,我们展示了重叠编码区域特有的一个新特征。通过对21个病毒基因组序列样本集的分析检测到了该特征,它表现为一个由某一阅读框编码的碱性氨基酸残基簇与相应重叠阅读框编码的一段酸性残基重复出现。对另一组病毒序列的计算机扫描表明,这一特征在其他几个已知的重叠ORF中也很常见,并由此预测丙型肝炎病毒(HGV)中存在一个新的重叠基因。与HGV基因组的其他基因区域相比,HGV中双功能编码区域的同义核苷酸替换率极低,这也支持了该区域的存在。对从假定的重叠基因推导的氨基酸序列的分析显示,碱性残基含量很高且存在核定位信号;这些特征表明,这个新的ORF可能表达一种类似核心的蛋白质。

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