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单纯疱疹病毒gB基因的猿猴疱疹病毒SA8同源物:图谱绘制、测序及与单纯疱疹病毒gB的比较。

The simian herpesvirus SA8 homologue of the herpes simplex virus gB gene: mapping, sequencing, and comparison to the HSV gB.

作者信息

Eberle R, Black D

机构信息

Department of Veterinary Parasitology, Microbiology, and Public Health, College of Veterinary Medicine, Oklahoma State University, Stillwater.

出版信息

Arch Virol. 1991;118(1-2):67-86. doi: 10.1007/BF01311304.

Abstract

The genomic location and DNA sequence of the simian herpesvirus SA8 gene encoding a homologue of the HSV1 gB glycoprotein was determined. Using a cloned gB gene of herpes simplex virus type 1 (HSV1) as probe in Southern blot hybridizations, the SA8 gB gene was localized to a 10-kbp KpnI fragment mapping in the unique long part of the genome. A 2.8 kbp, 68.4% GC segment of this fragment was sequenced. It contained a 2649 nucleotide ORF possibly encoding a 98.4 kDa polypeptide. The predicted amino acid sequence of the SA8 gB polypeptide is 78.4% and 78.9% identical to the sequence of the HSV1 and HSV2 gBs, respectively, and was 88.4% similar or identical to both HSV gB sequences. Structural characteristics predicted for the SA8 gB polypeptide were very similar to those of HSV1 gB. These included a hydrophobic signal sequence of 29 amino acids, conservation of all 10 cysteine residues and 5 of 6 potential N-linked glycosylation sites present in the HSV1 gB, a triple hydrophobic transmembrane domain, and a highly charged cytoplasmic tail region. Both hierarchical cluster analysis and phylogenetic analysis of sequences for gB polypeptides of 12 different herpesviruses demonstrated that the gB glycoprotein of SA8 is most closely related to the HSV gB glycoproteins. Comparison of these closely related gB sequences identified four regions in which non-conservative amino acid substitutions were clustered. Localized regions of the gB polypeptide were identified which are likely to be associated with the conserved structure/function of the polypeptide.

摘要

确定了编码与单纯疱疹病毒1型(HSV1)gB糖蛋白同源物的猴疱疹病毒SA8基因的基因组位置和DNA序列。在Southern印迹杂交中,使用克隆的单纯疱疹病毒1型(HSV1)gB基因作为探针,将SA8 gB基因定位到基因组独特长片段中的一个10 kbp KpnI片段上。对该片段的一个2.8 kbp、GC含量为68.4%的区段进行了测序。它包含一个2649个核苷酸的开放阅读框,可能编码一个98.4 kDa的多肽。SA8 gB多肽的预测氨基酸序列与HSV1和HSV2 gB序列的同一性分别为78.4%和78.9%,与两种HSV gB序列的相似性或同一性为88.4%。预测的SA8 gB多肽的结构特征与HSV1 gB非常相似。这些特征包括一个29个氨基酸的疏水信号序列、HSV1 gB中所有10个半胱氨酸残基和6个潜在N-连接糖基化位点中的5个的保守性、一个三重疏水跨膜结构域以及一个高度带电的胞质尾区。对12种不同疱疹病毒gB多肽序列的层次聚类分析和系统发育分析均表明,SA8的gB糖蛋白与HSV gB糖蛋白关系最为密切。对这些密切相关的gB序列进行比较,确定了四个非保守氨基酸取代聚集的区域。确定了gB多肽的局部区域,这些区域可能与多肽的保守结构/功能相关。

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