Martínez de Alba Angel Emilio, Sägesser Rudolf, Tabler Martin, Tsagris Mina
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Heraklion, Crete, Greece.
J Virol. 2003 Sep;77(17):9685-94. doi: 10.1128/jvi.77.17.9685-9694.2003.
For the identification of RNA-binding proteins that specifically interact with potato spindle tuber viroid (PSTVd), we subjected a tomato cDNA expression library prepared from viroid-infected leaves to an RNA ligand screening procedure. We repeatedly identified cDNA clones that expressed a protein of 602 amino acids. The protein contains a bromodomain and was termed viroid RNA-binding protein 1 (VIRP1). The specificity of interaction of VIRP1 with viroid RNA was studied by different methodologies, which included Northwestern blotting, plaque lift, and electrophoretic mobility shift assays. VIRP1 interacted strongly and specifically with monomeric and oligomeric PSTVd positive-strand RNA transcripts. Other RNAs, for example, U1 RNA, did not bind to VIRP1. Further, we could immunoprecipitate complexes from infected tomato leaves that contained VIRP1 and viroid RNA in vivo. Analysis of the protein sequence revealed that VIRP1 is a member of a newly identified family of transcriptional regulators associated with chromatin remodeling. VIRP1 is the first member of this family of proteins, for which a specific RNA-binding activity is shown. A possible role of VIRP1 in viroid replication and in RNA mediated chromatin remodeling is discussed.
为了鉴定与马铃薯纺锤块茎类病毒(PSTVd)特异性相互作用的RNA结合蛋白,我们对从感染类病毒的叶片制备的番茄cDNA表达文库进行了RNA配体筛选程序。我们反复鉴定出表达一种602个氨基酸的蛋白质的cDNA克隆。该蛋白质含有一个溴结构域,被命名为类病毒RNA结合蛋白1(VIRP1)。通过不同的方法研究了VIRP1与类病毒RNA相互作用的特异性,这些方法包括蛋白质印迹法、菌斑转移法和电泳迁移率变动分析。VIRP1与单体和寡聚体PSTVd正链RNA转录本强烈且特异性地相互作用。其他RNA,例如U1 RNA,不与VIRP1结合。此外,我们可以从感染的番茄叶片中免疫沉淀出体内含有VIRP1和类病毒RNA的复合物。对蛋白质序列的分析表明,VIRP1是与染色质重塑相关的新鉴定的转录调节因子家族的成员。VIRP1是该蛋白质家族的第一个成员,其显示出特异性的RNA结合活性。讨论了VIRP1在类病毒复制和RNA介导的染色质重塑中的可能作用。