Lin Xiaoyan, Thorne Lucy, Jin Zhinan, Hammad Loubna A, Li Serena, Deval Jerome, Goodfellow Ian G, Kao C Cheng
Department of Molecular and Cellular Biochemistry, Indiana University, Bloomington, IN 47405, USA.
Division of Virology, Department of Pathology, University of Cambridge, Addenbrookes Hospital, Hills Road CB2 2QQ, UK.
Nucleic Acids Res. 2015 Jan;43(1):446-60. doi: 10.1093/nar/gku1292. Epub 2014 Dec 17.
The replication enzyme of RNA viruses must preferentially recognize their RNAs in an environment that contains an abundance of cellular RNAs. The factors responsible for specific RNA recognition are not well understood, in part because viral RNA synthesis takes place within enzyme complexes associated with modified cellular membrane compartments. Recombinant RNA-dependent RNA polymerases (RdRps) from the human norovirus and the murine norovirus (MNV) were found to preferentially recognize RNA segments that contain the promoter and a short template sequence for subgenomic RNA synthesis. Both the promoter and template sequence contribute to stable RdRp binding, accurate initiation of the subgenomic RNAs and efficient RNA synthesis. Using a method that combines RNA crosslinking and mass spectrometry, residues near the template channel of the MNV RdRp were found to contact the hairpin RNA motif. Mutations in the hairpin contact site in the MNV RdRp reduced MNV replication and virus production in cells. This work demonstrates that the specific recognition of the norovirus subgenomic promoter is through binding by the viral RdRp.
RNA病毒的复制酶必须在含有大量细胞RNA的环境中优先识别其RNA。负责特异性RNA识别的因素尚未完全明确,部分原因是病毒RNA合成发生在与修饰的细胞膜区室相关的酶复合物中。研究发现,来自人诺如病毒和鼠诺如病毒(MNV)的重组RNA依赖性RNA聚合酶(RdRp)优先识别包含启动子和亚基因组RNA合成短模板序列的RNA片段。启动子和模板序列都有助于RdRp的稳定结合、亚基因组RNA的准确起始以及高效的RNA合成。通过结合RNA交联和质谱分析的方法,发现MNV RdRp模板通道附近的残基与发夹RNA基序接触。MNV RdRp中发夹接触位点的突变降低了细胞中的MNV复制和病毒产生。这项工作表明,诺如病毒亚基因组启动子的特异性识别是通过病毒RdRp的结合实现的。