Leopardi R, Hukkanen V, Vainionpää R, Salmi A A
Department of Virology, University of Turku, Finland.
J Virol. 1993 Feb;67(2):785-90. doi: 10.1128/JVI.67.2.785-790.1993.
The genomic 3' noncoding region (NCR) of nonsegmented negative-strand RNA viruses contains recognition site(s) for the polymerase complex, while the RNA plus-strand leader sequence (LS) is probably involved in RNA encapsidation. It is known that host-encoded factors play a role in transcription and replication of some of this group of viruses. Here we report that cellular proteins interact with the genomic 3' NCR and with the plus-strand LS RNA of an important human pathogen, measles virus (MV), a member of the family Paramyxoviridae. Using gel retardation assay and RNA footprinting analysis, we demonstrated that in Vero cells, host-encoded proteins bind specifically to domains within these two sequences. A polypeptide of about 20 kDa binding to the 3' NCR and two polypeptides of about 22 and 30 kDa interacting with plus-strand LS were detected by RNA-protein UV cross-linking. Different RNA-binding activities were found in cells differing in permissiveness to MV replication. The results suggest a role for host-encoded proteins in MV replication.
非节段性负链RNA病毒的基因组3'非编码区(NCR)含有聚合酶复合体的识别位点,而RNA正链前导序列(LS)可能参与RNA的包装。已知宿主编码因子在这类病毒中的一些病毒的转录和复制中发挥作用。在此我们报道,细胞蛋白与重要的人类病原体麻疹病毒(MV)(副粘病毒科的成员)的基因组3' NCR以及正链LS RNA相互作用。使用凝胶阻滞分析和RNA足迹分析,我们证明在Vero细胞中,宿主编码蛋白特异性结合这两个序列内的结构域。通过RNA-蛋白质紫外线交联检测到一种约20 kDa的多肽与3' NCR结合,以及两种约22 kDa和30 kDa的多肽与正链LS相互作用。在对MV复制允许性不同的细胞中发现了不同的RNA结合活性。结果表明宿主编码蛋白在MV复制中发挥作用。