首页> 外国专利> NOVEL REPLICATION COMPETENT HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 (HIV-2) PROVIRAL CLONE DESIGNATED HIV-2KR

NOVEL REPLICATION COMPETENT HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 (HIV-2) PROVIRAL CLONE DESIGNATED HIV-2KR

机译:具有复制能力的新型人类免疫缺陷病毒2型(HIV-2)临时克隆指定的HIV-2KR

摘要

A full-length infectious molecular clone, designated HIV-K, was obtained from a recombinant bacteriophage library constructed from HI-2PIE-infected MOLT-4/8 genomic DNA. Nucleotide sequence analysis of this clone demonstrated that the rev coding region extends for nearly 69 amino acid residues past the end of most other HIV-2/SIV rev genes. In addition, the long terminal repeat (LTR) contains a deletion of 9-10 bp, depending upon the nucleotide sequence alignment parameters, upstream from the SpI binding sites. This deletion is not present in other HIV-2/SIV isolates and is not similar to previously disclosed NFkB duplications in this region. The HIV-2KR LTR displays higher levels of basal transcriptional acitivty as compared to prototypical HIV-2 isolates. HIV-2KR is capable of infecting macaque peripheral blood lymphocytes (PBMCs) in vitro and produces a productive and persistant, albeit attenuated, infection in Macacca nemestrina. These proviral constructs are useful, inter alia, for the generation of in vitro diagnostic reagents, cell transcuction vectors, and the generation of HIV-2 based packaging cell lines.
机译:从由HI-2PIE感染的MOLT-4 / 8基因组DNA构建的重组噬菌体文库中获得了全长感染性分子克隆,称为HIV-K。该克隆的核苷酸序列分析表明,rev编码区延伸了超过大多数其他HIV-2 / SIV rev基因末端的近69个氨基酸残基。另外,取决于核苷酸序列比对参数,长末端重复序列(LTR)在SpI结合位点上游含有9-10bp的缺失。该缺失在其他HIV-2 / SIV分离株中不存在,并且与该区域先前公开的NFkB复制不相似。与典型的HIV-2分离株相比,HIV-2KR LTR显示出更高水平的基础转录活性。 HIV-2KR能够在体外感染猕猴外周血淋巴细胞(PBMC),并在马卡卡nemestrina中产生高效且持久的感染,尽管减弱了。这些前病毒构建体尤其可用于产生体外诊断试剂,细胞横切载体和产生基于HIV-2的包装细胞系。

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