Brunstein J, Astell C R
Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
J Virol. 1997 Dec;71(12):9087-95. doi: 10.1128/JVI.71.12.9087-9095.1997.
Prior analysis of minigenomes of minute virus of mice carried out by our laboratory indicated that sequences within the region of nucleotides 4489 to 4695, inboard of the 5' palindrome, are required for efficient DNA replication of the virus and are the site of specific interactions with unidentified factors present in a host cell nuclear extract (P. Tam and C. R. Astell, Virology 193:812-824, 1993; P. Tam and C. R. Astell, J. Virology 68:2840-2848, 1994). In order to examine this region in finer detail, a comprehensive library of linker-scanning mutants spanning the region was tested for the ability to support replication of minigenome constructs and for the ability to interact with host cell factors. Three short discrete sequence elements critical for replication competence were observed. Binding of host cell nuclear factors was localized to four sites, with two major complexes each appearing to have two binding sites within the region. All factor binding sites were found to be directly adjacent to or overlapping with sequence elements contributing to replication competence, and evidence suggesting a correlation between factor binding and minigenome replication is presented. A possible model is proposed for function of a viral origin within the region of the internal replication sequence which addresses the still-unresolved problem of how parvoviruses overcome the thermodynamic energy barrier involved in the rearrangement of the 5'-terminal palindrome from an extended form to a hairpin conformation.
我们实验室之前对小鼠微小病毒微型基因组的分析表明,病毒高效DNA复制需要5'回文序列内侧核苷酸4489至4695区域内的序列,该区域是与宿主细胞核提取物中未知因子发生特异性相互作用的位点(P. Tam和C. R. Astell,《病毒学》193:812 - 824,1993;P. Tam和C. R. Astell,《病毒学杂志》68:2840 - 2848,1994)。为了更详细地研究该区域,我们测试了一个跨越该区域的接头扫描突变体综合文库,以检测其支持微型基因组构建体复制的能力以及与宿主细胞因子相互作用的能力。观察到三个对复制能力至关重要的短离散序列元件。宿主细胞核因子的结合定位于四个位点,每个位点有两个主要复合物,每个复合物在该区域似乎有两个结合位点。发现所有因子结合位点都直接与有助于复制能力的序列元件相邻或重叠,并提供了因子结合与微型基因组复制之间存在相关性的证据。针对内部复制序列区域内病毒起源的功能提出了一个可能的模型,该模型解决了细小病毒如何克服5'末端回文序列从延伸形式重排为发夹构象所涉及的热力学能量障碍这一尚未解决的问题。