Crescenzo-Chaigne Bernadette, Barbezange Cyril, van der Werf Sylvie
Unité de Génétique Moléculaire des Virus Respiratoires, URA 3015 CNRS, EA 302 Université Paris Diderot, Institut Pasteur, Paris, France.
Virol J. 2008 Oct 30;5:132. doi: 10.1186/1743-422X-5-132.
The transcription/replication of the influenza viruses implicate the terminal nucleotide sequences of viral RNA, which comprise sequences at the extremities conserved among the genomic segments as well as variable 3' and 5' non-coding (NC) regions. The plasmid-based system for the in vivo reconstitution of functional ribonucleoproteins, upon expression of viral-like RNAs together with the nucleoprotein and polymerase proteins has been widely used to analyze transcription/replication of influenza viruses. It was thus shown that the type A polymerase could transcribe and replicate type A, B, or C vRNA templates whereas neither type B nor type C polymerases were able to transcribe and replicate type A templates efficiently. Here we studied the importance of the NC regions from the seven segments of type C influenza virus for efficient transcription/replication by the type A and C polymerases.
The NC sequences of the seven genomic segments of the type C influenza virus C/Johannesburg/1/66 strain were found to be more variable in length than those of the type A and B viruses. The levels of transcription/replication of viral-like vRNAs harboring the NC sequences of the respective type C virus segments flanking the CAT reporter gene were comparable in the presence of either type C or type A polymerase complexes except for the NS and PB2-like vRNAs. For the NS-like vRNA, the transcription/replication level was higher after introduction of a U residue at position 6 in the 5' NC region as for all other segments. For the PB2-like vRNA the CAT expression level was particularly reduced with the type C polymerase. Analysis of mutants of the 5' NC sequence in the PB2-like vRNA, the shortest 5' NC sequence among the seven segments, showed that additional sequences within the PB2 ORF were essential for the efficiency of transcription but not replication by the type C polymerase complex.
In the context of a PB2-like reporter vRNA template, the sequence upstream the polyU stretch plays a role in the transcription/replication process by the type C polymerase complex.
流感病毒的转录/复制涉及病毒RNA的末端核苷酸序列,其包括基因组片段末端保守的序列以及可变的3'和5'非编码(NC)区域。基于质粒的系统用于在体内重建功能性核糖核蛋白,当病毒样RNA与核蛋白和聚合酶蛋白一起表达时,已被广泛用于分析流感病毒的转录/复制。结果表明,A型聚合酶可以转录和复制A、B或C型vRNA模板,而B型和C型聚合酶均不能有效转录和复制A型模板。在此,我们研究了C型流感病毒七个片段的NC区域对于A型和C型聚合酶高效转录/复制的重要性。
发现C型流感病毒C/约翰内斯堡/1/66株七个基因组片段的NC序列在长度上比A型和B型病毒的NC序列更具变异性。在存在C型或A型聚合酶复合物的情况下,携带CAT报告基因两侧相应C型病毒片段NC序列的病毒样vRNA的转录/复制水平相当,但NS和PB2样vRNA除外。对于NS样vRNA,与所有其他片段一样,在5'NC区域的第6位引入U残基后,转录/复制水平更高。对于PB2样vRNA,C型聚合酶的CAT表达水平特别降低。对PB2样vRNA中5'NC序列的突变体进行分析,PB2样vRNA是七个片段中最短的5'NC序列,结果表明PB2开放阅读框内的额外序列对于C型聚合酶复合物的转录效率至关重要,但对复制效率无影响。
在PB2样报告vRNA模板的背景下,polyU延伸上游的序列在C型聚合酶复合物的转录/复制过程中起作用。