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用于亚基因组mRNA合成的辛德毕斯病毒启动子的宿主依赖性进化。

Host-dependent evolution of the Sindbis virus promoter for subgenomic mRNA synthesis.

作者信息

Hertz J M, Huang H V

机构信息

Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110-1093, USA.

出版信息

J Virol. 1995 Dec;69(12):7775-81. doi: 10.1128/JVI.69.12.7775-7781.1995.

Abstract

Alphaviruses are alternately transmitted between arthropod and vertebrate hosts. In each host, the virus transcribes a subgenomic mRNA that encodes the viral structural proteins which encapsidate the genome to form progeny virions. Transcription initiates at an internal site called the promoter. To determine if promoter utilization varies in mammalian versus mosquito cells, we used these cells as hosts to select for active promoters among a library of different mutant promoters. Compared with that in BHK-21 cells, selection was more rapid in mosquito (C7-10) cells, with much less diversity of promoters remaining after fewer passages. Thus, promoter selection is host dependent. With further passaging, both BHK-21 and C7-10 cells selected for similar sequences that closely resemble the wild-type promoter sequence. The difference in the rates of selection is not because BHK-21-derived promoters cannot function in mosquito cells. Instead, part of the host dependence is probably due to posttranscriptional differences between BHK-21 and C7-10 cells that may require more active promoters in mosquito cells. Part of the host dependence may also be attributed to the decreased rate of transcription versus that of replication in mosquito cells. This change in regulation of subgenomic to genomic RNA synthesis appears to correlate with the extent of cleavage or pausing of the genomic RNA synthesis at or close to the promoter.

摘要

甲病毒在节肢动物宿主和脊椎动物宿主之间交替传播。在每个宿主中,病毒转录一种亚基因组mRNA,该mRNA编码病毒结构蛋白,这些结构蛋白包裹基因组以形成子代病毒粒子。转录起始于一个称为启动子的内部位点。为了确定启动子的利用在哺乳动物细胞和蚊子细胞中是否存在差异,我们以这些细胞作为宿主,在不同突变启动子文库中筛选活跃启动子。与BHK-21细胞相比,在蚊子(C7-10)细胞中的筛选更快,传代次数较少后剩余的启动子多样性要少得多。因此,启动子的选择取决于宿主。随着进一步传代,BHK-21细胞和C7-10细胞都选择了与野生型启动子序列非常相似的相似序列。选择速率的差异并不是因为源自BHK-21的启动子在蚊子细胞中不能发挥作用。相反,宿主依赖性的部分原因可能是BHK-21细胞和C7-10细胞之间的转录后差异,这可能需要蚊子细胞中有更活跃的启动子。宿主依赖性的部分原因也可能归因于蚊子细胞中转录速率相对于复制速率的降低。亚基因组到基因组RNA合成调控的这种变化似乎与基因组RNA合成在启动子处或其附近的切割或暂停程度相关。

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