Schiebel W, Pélissier T, Riedel L, Thalmeir S, Schiebel R, Kempe D, Lottspeich F, Sänger H L, Wassenegger M
Max-Planck-Institut für Biochemie, Abteilung Viroidforschung, D-82152 Martinsried, Germany.
Plant Cell. 1998 Dec;10(12):2087-101. doi: 10.1105/tpc.10.12.2087.
A 3600-bp RNA-directed RNA polymerase (RdRP)-specific cDNA comprising an open reading frame (ORF) of 1114 amino acids was isolated from tomato. The putative protein encoded by this ORF does not share homology with any characterized proteins. Antibodies that were raised against synthetic peptides whose sequences have been deduced from the ORF were shown to specifically detect the 127-kD tomato RdRP protein. The immunoresponse to the antibodies correlated with the enzymatic activity profile of the RdRP after chromatography on Q-, poly(A)-, and poly(U)-Sepharose, hydroxyapatite, and Sephadex G-200 columns. DNA gel blot analysis revealed a single copy of the RdRP gene in tomato. RdRP homologs from petunia, Arabidopsis, tobacco, and wheat were identified by using polymerase chain reaction. A sequence comparison indicated that sequences homologous to RdRP are also present in the yeast Schizosaccharomyces pombe and in the nematode Caenorhabditis elegans. The previously described induction of RdRP activity upon viroid infection is shown to be correlated with an increased steady state level of the corresponding mRNA. The possible involvement of this heretofore functionally elusive plant RNA polymerase in homology-dependent gene silencing is discussed.
从番茄中分离出一个3600bp的RNA指导的RNA聚合酶(RdRP)特异性cDNA,其包含一个1114个氨基酸的开放阅读框(ORF)。该ORF编码的推定蛋白与任何已鉴定的蛋白均无同源性。针对从该ORF推导的序列合成的肽段产生的抗体,可特异性检测127-kD的番茄RdRP蛋白。在Q-琼脂糖、聚(A)-琼脂糖、聚(U)-琼脂糖、羟基磷灰石和葡聚糖G-200柱上进行层析后,对抗体的免疫反应与RdRP的酶活性谱相关。DNA凝胶印迹分析表明番茄中RdRP基因只有一个拷贝。利用聚合酶链反应鉴定了矮牵牛、拟南芥、烟草和小麦中的RdRP同源物。序列比较表明,与RdRP同源的序列也存在于酵母粟酒裂殖酵母和线虫秀丽隐杆线虫中。先前描述的类病毒感染后RdRP活性的诱导与相应mRNA稳态水平的增加相关。本文还讨论了这种迄今为止功能尚不清楚的植物RNA聚合酶在同源依赖性基因沉默中的可能作用。