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人类泡沫病毒pol基因表达为前体多聚蛋白Pro-Pol,而非Gag-Pol融合蛋白。

The human foamy virus pol gene is expressed as a Pro-Pol polyprotein and not as a Gag-Pol fusion protein.

作者信息

Löchelt M, Flügel R M

机构信息

Abteilung Retrovirale Genexpression, Forschungsschwerpunkt Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

出版信息

J Virol. 1996 Feb;70(2):1033-40. doi: 10.1128/JVI.70.2.1033-1040.1996.

Abstract

It has been reported recently that the human foamy virus (HFV) Pol polyprotein of 120 kDa is synthesized in the absence of the active HFV aspartic protease. To gain more information on how the 120-kDa Pro-Pol protein is synthesized, mutant HFV genomes were constructed and the resulting proviruses were analyzed with respect to HFV pol expression and infectivity. HFV proviruses that contain termination codons in the nucleocapsid domain of gag and thus lack a gag-pol overlap region assumed to be required for translational frameshifting, nevertheless expressed the 120-kDa Pro-Pol precursor, the 80-kDa reverse transcriptase/RNase H, and a 40-kDa integrase in amounts similar to those observed for wild-type genomes. Since a Gag-independent expression of authentic Pol proteins was detectable in cells transfected with eukaryotic HFV pol expression plasmids, the data indicate that the HFV Pol precursor of 120 kDa is expressed independently of Gag by a mechanism that does not rely on ribosomal frameshifting, since the postulated HFV Gag-Pol protein of 190 kDa was not detectable under the conditions used. Furthermore, replacement of the Met residue by Thr at position 9 in pol within the gag-pol overlap region resulted in strongly reduced HFV Pol polyprotein expression and infectivity of the resulting proviruses. This Met residue of pol conserved in foamy virus sequences is the likely candidate for translational initiation of the 120-kDa Pro-Pol polyprotein. trans complementation of the HFV mutant with the Met-to-Thr substitution in the pol gene by a eukaryotic plasmid that expressed the HFV Pro-Pol protein resulted in partial recovery of infectivity. When HFV pol was fused in frame to gag, an engineered 190-kDa Gag-Pol fusion protein was formed and the enzymatic activity of the HFV protease was partially retained. The results imply that HFV is the first retrovirus that expresses a Pol polyprotein without formation of a Gag-Pol fusion protein.

摘要

最近有报道称,在没有活性人泡沫病毒(HFV)天冬氨酸蛋白酶的情况下,会合成120 kDa的HFV Pol多聚蛋白。为了获取更多关于120 kDa前体Pol蛋白如何合成的信息,构建了突变型HFV基因组,并对所得前病毒的HFV pol表达和感染性进行了分析。在gag的核衣壳结构域中含有终止密码子从而缺乏假定的翻译移码所需的gag-pol重叠区域的HFV前病毒,仍然表达了120 kDa的前体Pol蛋白、80 kDa的逆转录酶/RNase H和40 kDa的整合酶,其表达量与野生型基因组中观察到的相似。由于在用真核HFV pol表达质粒转染的细胞中可检测到不依赖Gag的真实Pol蛋白表达,数据表明120 kDa的HFV Pol前体通过一种不依赖核糖体移码的机制独立于Gag表达,因为在所使用的条件下未检测到假定的190 kDa的HFV Gag-Pol蛋白。此外,在gag-pol重叠区域内pol基因的第9位将Met残基替换为Thr导致HFV Pol多聚蛋白表达大幅降低以及所得前病毒的感染性降低。在泡沫病毒序列中保守的pol的这个Met残基可能是120 kDa前体Pol多聚蛋白翻译起始的候选位点。用表达HFV Pro-Pol蛋白的真核质粒对pol基因中Met替换为Thr的HFV突变体进行反式互补,导致感染性部分恢复。当HFV pol与gag框内融合时,形成了一种工程化的190 kDa Gag-Pol融合蛋白,并且HFV蛋白酶的酶活性部分得以保留。结果表明,HFV是第一种表达Pol多聚蛋白而不形成Gag-Pol融合蛋白的逆转录病毒。

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