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猴泡沫病毒1型5'前导区的突变分析

Mutational analysis of the 5' leader region of simian foamy virus type 1.

作者信息

Park J, Mergia A

机构信息

Department of Pathobiology, College of Veterinary Medicine, University of Florida, Gainesville, Florida 32610, USA.

出版信息

Virology. 2000 Aug 15;274(1):203-12. doi: 10.1006/viro.2000.0423.

Abstract

The sequence within the 5' untranslated region of the retroviral genome contains important cis elements for many steps in viral replication. There is limited information available on the role of this region in foamy virus replication. Similar to other retroviruses, the 5' untranslated region of foamy viruses predicts extensive RNA secondary structure. Serial mutations that could change parts of the predicted secondary structure were introduced in the 5' leader sequence including the R-U5 region of simian foamy virus type 1 (SFV-1) to investigate their role in virus genome packaging and virus replication. Point mutations in the R-U5 regions at nucleotide positions 7-12 (I), 241-243 (B), and 256-257 (D) had no effect on virus replication. Base substitution mutation at positions 193-195 (C), however, severely impaired virus replication. Deletion of sequences in the leader region, between the primer-binding site and the gag gene, at positions 364-399 (d1), 397-435 (d2), or 364-435 (d3), which included sequences for RNA genome dimerization, also blocked SFV-1 replication. Interestingly, none of these mutations affected genome packaging or the synthesis of viral transcripts, suggesting that a step(s) of virus replication following packaging is affected. The region between the primer-binding site and the gag gene, therefore, is not essential for foamy virus genome packaging. Furthermore, the cis-acting elements for genome dimerization and packaging appear to be localized in separate regions for foamy viruses.

摘要

逆转录病毒基因组5'非翻译区内的序列包含病毒复制多个步骤所需的重要顺式作用元件。关于该区域在泡沫病毒复制中的作用,目前已知信息有限。与其他逆转录病毒相似,泡沫病毒的5'非翻译区可形成广泛的RNA二级结构。为了研究其在病毒基因组包装和病毒复制中的作用,我们在1型猿猴泡沫病毒(SFV-1)的5'前导序列(包括R-U5区域)中引入了一系列可改变预测二级结构部分区域的突变。R-U5区域核苷酸位置7-12(I)、241-243(B)和256-257(D)处的点突变对病毒复制没有影响。然而,193-195(C)位置的碱基替换突变严重损害了病毒复制。删除引物结合位点与gag基因之间前导区域364-399(d1)、397-435(d2)或364-435(d3)位置的序列(包括RNA基因组二聚化序列)也阻断了SFV-1的复制。有趣的是,这些突变均未影响基因组包装或病毒转录本的合成,这表明包装后病毒复制的某个步骤受到了影响。因此,引物结合位点与gag基因之间的区域对于泡沫病毒基因组包装并非必不可少。此外,泡沫病毒基因组二聚化和包装的顺式作用元件似乎位于不同区域。

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