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利用变性梯度凝胶电泳和PCR产物直接自动化DNA测序对HIV-1序列多样性进行快速鉴定。

Rapid characterization of HIV-1 sequence diversity using denaturing gradient gel electrophoresis and direct automated DNA sequencing of PCR products.

作者信息

Andersson B, Ying J H, Lewis D E, Gibbs R A

机构信息

Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030.

出版信息

PCR Methods Appl. 1993 May;2(4):293-300. doi: 10.1101/gr.2.4.293.

Abstract

A direct method for visualization and isolation of sequence variants of human immunodeficiency virus type 1 (HIV-1) utilizing denaturing gradient gel electrophoresis (DGGE) combined with automated direct DNA sequencing was developed. Two fragments from the env gene and one from the nef gene of HIV-1, which together constitute approximately 1.0 kb of sequence, were amplified by PCR and analyzed. HIV-1 variants from each region were resolved and excised from the gel; this was followed by direct sequencing of different viral variants. In 9 infected patients, a limited number of dominant sequence variants could be seen in the three regions, together with a faint background of minor variants. The use of DGGE makes it possible to obtain a direct estimate of overall HIV-1 sequence diversity within patient samples without an intermediate DNA cloning step.

摘要

开发了一种利用变性梯度凝胶电泳(DGGE)结合自动直接DNA测序来可视化和分离1型人类免疫缺陷病毒(HIV-1)序列变异体的直接方法。通过聚合酶链反应(PCR)扩增并分析了HIV-1 env基因的两个片段和nef基因的一个片段,这些片段共同构成了约1.0 kb的序列。从每个区域分离出HIV-1变异体并从凝胶中切下;随后对不同的病毒变异体进行直接测序。在9名感染患者中,在这三个区域可以看到数量有限的优势序列变异体,以及少量变异体组成的微弱背景。DGGE的使用使得在无需中间DNA克隆步骤的情况下,直接估计患者样本中HIV-1的总体序列多样性成为可能。

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