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通过同源重组产生杂交人类免疫缺陷病毒。

Generation of hybrid human immunodeficiency virus by homologous recombination.

作者信息

Srinivasan A, York D, Jannoun-Nasr R, Kalyanaraman S, Swan D, Benson J, Bohan C, Luciw P A, Schnoll S, Robinson R A

机构信息

Retrovirus Diseases Branch, Centers for Disease Control, Atlanta, GA 30333.

出版信息

Proc Natl Acad Sci U S A. 1989 Aug;86(16):6388-92. doi: 10.1073/pnas.86.16.6388.

Abstract

Human immunodeficiency virus (HIV) type 1, isolated from diverse sources, exhibits genomic diversity. The mechanisms by which the genomic diversity takes place in individuals exposed to multiple virus isolates is yet to be elucidated. Genetic variation, in general, might result from mutagenic events such as point mutations, rearrangements (insertions and deletions), and recombination. In an attempt to evaluate the process of genetic diversity, we designed experiments to analyze recombination between HIV DNAs by using DNA transfection in cell cultures. Here we report the successful recombination between truncated HIV proviral DNAs with an overlap homology of 53 base pairs that leads to the formation of viable hybrid virus. Recombination was also seen between exogenous DNA introduced into cells and homologous HIV sequences resident in the cells. These results indicate that recombination among various HIV isolates may play a significant role in the generation of genetic diversity of HIV. Further, the method used here enables the construction of hybrid HIV genomes to identify the viral determinants responsible for tropism, replication, and cytopathic effects.

摘要

从不同来源分离出的1型人类免疫缺陷病毒(HIV)呈现出基因组多样性。在接触多种病毒分离株的个体中,基因组多样性发生的机制尚待阐明。一般来说,遗传变异可能源于诱变事件,如点突变、重排(插入和缺失)以及重组。为了评估遗传多样性的过程,我们设计了实验,通过在细胞培养中进行DNA转染来分析HIV DNA之间的重组。在此,我们报告了截短的HIV前病毒DNA之间成功发生重组,其重叠同源性为53个碱基对,导致形成有活力的杂交病毒。在导入细胞的外源DNA与细胞内存在的同源HIV序列之间也观察到了重组。这些结果表明,各种HIV分离株之间的重组可能在HIV遗传多样性的产生中发挥重要作用。此外,这里使用的方法能够构建杂交HIV基因组,以鉴定负责嗜性、复制和细胞病变效应的病毒决定因素。

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