Definition of the minimal viral components required for the initiation of unprimed RNA synthesis by influenza virus RNA polymerase

被引:64
|
作者
Lee, MTM
Bishop, K
Medcalf, L
Elton, D
Digard, P
Tiley, L
机构
[1] Univ Cambridge, Ctr Vet Sci, Cambridge CB3 0ES, England
[2] Univ Cambridge, Dept Pathol, Div Virol, Cambridge CB2 1QP, England
基金
英国惠康基金;
关键词
D O I
10.1093/nar/30.2.429
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The first 11 nt at the 5' end of influenza virus genomic RNA were shown to be both necessary and sufficient for specific binding by the influenza virus polymerase. A novel in vitro transcription assay, in which the polymerase was bound to paramagnetic beads via a biotinylated 5'-vRNA oligonucleotide, was used to study the activities of different forms of the polymerase. Complexes composed of co-expressed PB1/PB2/PA proteins and a sub-complex composed of PB1/PA bound to the 5'-vRNA oligonucleotide, whereas PB1 expressed alone did not. The enriched 5'-vRNA/PB1/PB2/PA complex was highly active for ApG and globin mRNA primed transcription on a model 3'-vRNA template. RNA synthesis in the absence of added primers produced products with 5'-terminal tri- or diphosphate groups, indicating that genuine unprimed initiation of transcription also occurred. No transcriptase activity was detected for the PB1/PA complex. These results demonstrate a role for PA in the enhancement of 5' end binding activity of PB1, a role for PB2 in the assembly of a polymerase complex able to perform both cap-dependent and -independent synthesis and that NP is not required for the initiation of replicative transcription.
引用
收藏
页码:429 / 438
页数:10
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