Carpenter C D, Cascone P J, Simon A E
Department of Biochemistry, University of Massachusetts, Amherst 01003.
Virology. 1991 Aug;183(2):595-601. doi: 10.1016/0042-6822(91)90988-n.
Turnip crinkle virus (TCV) is associated with many subviral RNAs including satellite (sat-) RNAs which require a helper virus for infectivity. When plants were inoculated with TCV and transcripts of TCV sat-RNA C containing deletions of 3 to 8 nucleotides beginning at position 100 and extending toward the 5' end, some of the sat-RNA isolated from plants migrated more slowly than expected on denaturing polyacrylamide gels. Cleavage of the sat-RNA into two segments by digestion with RNase H following hybridization to an oligonucleotide complementary to internal sat-RNA sequence indicated that the 5' one-third of the molecule was involved in the abnormal gel migration. Sat-RNAs derived from transcripts with a deletion of bases in position 96-100 were cloned. Sequencing of the cDNAs revealed that the aberrant migration of the sat-RNAs was due to the presence of variable lengths of poly(U) 10 nucleotides downstream from the deletion at a position which already contained five U residues. Deletions extending toward the 3' end in the same region did not result in poly(U) additions. Mutations in the original five U residues along with the 5' deletions also did not lead to poly(U) additions. The insertion of poly(U) in TCV sat-RNA C may be a new example of replicase stuttering with the distinction that it only occurs following specific upstream mutations.
芜菁皱缩病毒(TCV)与许多亚病毒RNA有关,包括卫星(sat-)RNA,其感染性需要辅助病毒。当用TCV和从第100位开始向5'端缺失3至8个核苷酸的TCV sat-RNA C转录本接种植物时,从植物中分离出的一些sat-RNA在变性聚丙烯酰胺凝胶上的迁移速度比预期的要慢。在与与内部sat-RNA序列互补的寡核苷酸杂交后,用RNase H消化将sat-RNA切割成两个片段,这表明分子的5'三分之一参与了异常的凝胶迁移。克隆了来自在96 - 100位缺失碱基的转录本的sat-RNA。cDNA测序表明,sat-RNA的异常迁移是由于在已经含有五个U残基的位置,缺失下游存在可变长度的聚(U)10核苷酸。在同一区域向3'端延伸的缺失不会导致聚(U)添加。原始五个U残基中的突变以及5'端缺失也不会导致聚(U)添加。在TCV sat-RNA C中插入聚(U)可能是复制酶打滑的一个新例子,其区别在于它仅在特定的上游突变后发生。