Gillian A L, Schmechel S C, Livny J, Schiff L A, Nibert M L
Department of Biochemistry and Institute for Molecular Virology, The College of Agricultural and Life Sciences, University of Wisconsin-Madison, 53706, USA.
J Virol. 2000 Jul;74(13):5939-48. doi: 10.1128/jvi.74.13.5939-5948.2000.
Reovirus nonstructural protein sigmaNS interacts with reovirus plus-strand RNAs in infected cells, but little is known about the nature of those interactions or their roles in viral replication. In this study, a recombinant form of sigmaNS was analyzed for in vitro binding to nucleic acids using gel mobility shift assays. Multiple units of sigmaNS bound to single-stranded RNA molecules with positive cooperativity and with each unit covering about 25 nucleotides at saturation. The sigmaNS protein did not bind preferentially to reovirus RNA over nonreovirus RNA in competition experiments but did bind preferentially to single-stranded over double-stranded nucleic acids and with a slight preference for RNA over DNA. In addition, sigmaNS bound to single-stranded RNA to which a 19-base DNA oligonucleotide was hybridized at either end or near the middle. When present in saturative amounts, sigmaNS displaced this oligonucleotide from the partial duplex. The strand displacement activity did not require ATP hydrolysis and was inhibited by MgCl(2), distinguishing it from a classical ATP-dependent helicase. These properties of sigmaNS are similar to those of single-stranded DNA binding proteins that are known to participate in genomic DNA replication, suggesting a related role for sigmaNS in replication of the reovirus RNA genome.
呼肠孤病毒非结构蛋白σNS在受感染细胞中与呼肠孤病毒正链RNA相互作用,但对于这些相互作用的性质及其在病毒复制中的作用知之甚少。在本研究中,使用凝胶迁移率变动分析对重组形式的σNS进行体外核酸结合分析。多个σNS单元以正协同性结合到单链RNA分子上,每个单元在饱和时覆盖约25个核苷酸。在竞争实验中,σNS蛋白对呼肠孤病毒RNA的结合并不优先于非呼肠孤病毒RNA,但确实优先结合单链核酸而非双链核酸,并且对RNA的偏好略高于DNA。此外,σNS结合到在两端或中间附近与19个碱基的DNA寡核苷酸杂交的单链RNA上。当以饱和量存在时,σNS从部分双链体中置换出该寡核苷酸。链置换活性不需要ATP水解,并受到MgCl₂的抑制,这使其与经典的ATP依赖性解旋酶区分开来。σNS的这些特性与已知参与基因组DNA复制的单链DNA结合蛋白的特性相似,表明σNS在呼肠孤病毒RNA基因组复制中具有相关作用。