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禽逆转录病毒的env基因:核苷酸序列和分子重组体确定宿主范围决定因素

env genes of avian retroviruses: nucleotide sequence and molecular recombinants define host range determinants.

作者信息

Bova C A, Manfredi J P, Swanstrom R

出版信息

Virology. 1986 Jul 30;152(2):343-54. doi: 10.1016/0042-6822(86)90137-6.

Abstract

The env gene of avian sarcoma and leukosis retroviruses is allelic in the virus population permitting the virus to use different host cell receptors. This polymorphism has allowed the classification of these viruses into different subgroups. In order to understand further the role of viral sequences involved in determining this host range phenomenon, we constructed molecular recombinants between subgroup A, B, and E viruses and showed that the host range determinant defining subgroup specificity was located within a 1.1-kb region of the genome that included most of the coding region for the env gene product gp85. We also determined the nucleotide sequence of the region of the env gene encoding gp85 for virus isolates representing subgroup A and B viruses. We compared the predicted amino acid sequences of gp85 to themselves and to the previously published sequences of subgroup B, C, and E env genes. Based on these comparisons, we draw the following conclusions: Within the gp85 coding domain, there are four variable regions (VR-1 to VR-4) ranging in size from 9 to 52 amino acids. The variable regions are located in the same relative positions for each of the env gene alleles compared. The variable regions range in homology from 42% (A compared to B) to 57% (C compared to E) in pairwise comparisons; the flanking conserved domains are on average 95% homologous. The sequences of three different subgroup B virus isolates are highly homologous in both the conserved and variable regions. Secondary structure predictions suggest that gp85 is composed mostly of beta sheet topology. Hydrophilic loops within the variable regions may define sites of receptor interaction and binding sites for subgroup specific neutralizing antibodies.

摘要

禽肉瘤和白血病逆转录病毒的env基因在病毒群体中是等位基因,这使得病毒能够利用不同的宿主细胞受体。这种多态性使得这些病毒能够被分为不同的亚组。为了进一步了解参与决定这种宿主范围现象的病毒序列的作用,我们构建了A、B和E亚组病毒之间的分子重组体,并表明定义亚组特异性的宿主范围决定因素位于基因组的一个1.1 kb区域内,该区域包括env基因产物gp85的大部分编码区。我们还确定了代表A和B亚组病毒的病毒分离株中编码gp85的env基因区域的核苷酸序列。我们将gp85的预测氨基酸序列与其自身以及先前发表的B、C和E亚组env基因序列进行了比较。基于这些比较,我们得出以下结论:在gp85编码域内,有四个可变区(VR-1至VR-4),大小从9到52个氨基酸不等。对于所比较的每个env基因等位基因,可变区位于相同的相对位置。在成对比较中,可变区的同源性范围从42%(A与B相比)到57%(C与E相比);侧翼保守结构域平均同源性为95%。三种不同的B亚组病毒分离株的序列在保守区和可变区都高度同源。二级结构预测表明gp85主要由β折叠拓扑结构组成。可变区内的亲水环可能定义了受体相互作用的位点以及亚组特异性中和抗体的结合位点。

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