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参与芜菁皱缩病毒亚病毒RNA复制和病毒粒子积累的短内部序列。

Short internal sequences involved in replication and virion accumulation in a subviral RNA of turnip crinkle virus.

作者信息

Sun Xiaoping, Zhang Guohua, Simon Anne E

机构信息

Department of Cell Biology and Molecular Genetics, University of Maryland College Park, College Park, Maryland 20742, USA.

出版信息

J Virol. 2005 Jan;79(1):512-24. doi: 10.1128/JVI.79.1.512-524.2005.

Abstract

cis-acting sequences and structural elements in untranslated regions of viral genomes allow viral RNA-dependent RNA polymerases to correctly initiate and transcribe asymmetric levels of plus and minus strands during replication of plus-sense RNA viruses. Such elements include promoters, enhancers, and transcriptional repressors that may require interactions with distal RNA sequences for function. We previously determined that a non-sequence-specific hairpin (M1H) in the interior of a subviral RNA (satC) associated with Turnip crinkle virus is required for fitness and that its function might be to bridge flanking sequences (X. Sun and A. E. Simon, J. Virol. 77:7880-7889, 2003). To establish the importance of the flanking sequences in replication and satC-specific virion repression, segments on both sides of M1H were randomized and subjected to in vivo functional selection (in vivo SELEX). Analyses of winning (functional) sequences revealed three different conserved elements within the segments that could be specifically assigned roles in replication, virion repression, or both. One of these elements was also implicated in the molecular switch that releases the 3' end from its interaction with the repressor hairpin H5, which is possibly involved in controlling the level of minus-strand synthesis.

摘要

病毒基因组非翻译区中的顺式作用序列和结构元件,使得病毒RNA依赖的RNA聚合酶在正链RNA病毒复制过程中能够正确起始并转录不对称水平的正链和负链。这些元件包括启动子、增强子和转录抑制因子,其功能可能需要与远端RNA序列相互作用。我们之前确定,与芜菁皱缩病毒相关的亚病毒RNA(satC)内部的一个非序列特异性发夹结构(M1H)对于病毒存活能力是必需的,其功能可能是连接侧翼序列(X. Sun和A. E. Simon,《病毒学杂志》77:7880 - 7889,2003年)。为了确定侧翼序列在复制和satC特异性病毒粒子抑制中的重要性,M1H两侧的片段被随机化并进行体内功能筛选(体内SELEX)。对胜出(功能性)序列的分析揭示了这些片段内三个不同的保守元件,它们可被明确赋予在复制、病毒粒子抑制或两者中的作用。其中一个元件还与将3'端从其与抑制性发夹H5的相互作用中释放出来的分子开关有关,这可能参与控制负链合成水平。

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