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一种独特的人类免疫缺陷病毒分离株的分子克隆及初级核苷酸序列分析显示,其基因组序列存在显著差异。

Molecular cloning and primary nucleotide sequence analysis of a distinct human immunodeficiency virus isolate reveal significant divergence in its genomic sequences.

作者信息

Desai S M, Kalyanaraman V S, Casey J M, Srinivasan A, Andersen P R, Devare S G

出版信息

Proc Natl Acad Sci U S A. 1986 Nov;83(21):8380-4. doi: 10.1073/pnas.83.21.8380.

Abstract

In an effort to evaluate data on genomic relatedness among the various human immunodeficiency viruses (HIVs), we have molecularly cloned a virus isolate designated HIV (CDC-451). Preliminary characterization of the HIV (CDC-451) clone indicated that the restriction enzyme map was distinct from those of other known HIV isolates. Analysis of the primary nucleotide sequence of the regions encoding the structural proteins and comparison with sequences known for other HIV isolates indicated substantial differences for HIV (CDC-451). The sequences encoding the group-specific antigen gene, although they showed some variation, were conserved to a greater extent than were those encoding envelope proteins. In the envelope gene sequences, most of the changes (up to 24.5% divergence) were located in the amino-terminal region encoding a glycoprotein with a Mr of 120,000. The carboxyl-terminal region, encoding a protein of Mr 41,000, was more highly conserved. The variation in the sequences encoding envelope proteins may have important implications for the antigenic properties and/or pathogenicity of the disease and for its detection and ultimate eradication.

摘要

为了评估各种人类免疫缺陷病毒(HIV)之间基因组相关性的数据,我们对一株命名为HIV(CDC - 451)的病毒分离株进行了分子克隆。HIV(CDC - 451)克隆的初步特征表明,其限制性酶切图谱与其他已知HIV分离株的图谱不同。对编码结构蛋白区域的初级核苷酸序列进行分析,并与其他HIV分离株的已知序列进行比较,结果表明HIV(CDC - 451)存在显著差异。编码群特异性抗原基因的序列虽然有一些变化,但比编码包膜蛋白的序列在更大程度上保持保守。在包膜基因序列中,大多数变化(差异高达24.5%)位于编码分子量为120,000的糖蛋白的氨基末端区域。编码分子量为41,000的蛋白的羧基末端区域则更为保守。编码包膜蛋白的序列变化可能对该疾病的抗原特性和/或致病性以及对其检测和最终根除具有重要意义。

相似文献

6
Genetic variability in human immunodeficiency viruses.人类免疫缺陷病毒的基因变异性。
Ann N Y Acad Sci. 1987;511:376-84. doi: 10.1111/j.1749-6632.1987.tb36266.x.

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