期刊
JOURNAL OF VIROLOGY
卷 85, 期 13, 页码 6197-6204出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.00277-11
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资金
- Ministry of Education, Culture, Sports, Science, and Technology of Japan
- Japanese Society for the Promotion of Science
- Grants-in-Aid for Scientific Research [22790438, 09J00964, 20249025] Funding Source: KAKEN
The influenza virus RNA-dependent RNA polymerase is capable of initiating replication but mainly catalyzes abortive RNA synthesis in the absence of viral and host regulatory factors. Previously, we reported that IREF-1/minichromosome maintenance (MCM) complex stimulates a de novo initiated replication reaction by stabilizing an initiated replication complex through scaffolding between the viral polymerase and nascent cRNA to which MCM binds. In addition, several lines of genetic and biochemical evidence suggest that viral nucleoprotein (NP) is involved in successful replication. Here, using cell-free systems, we have shown the precise stimulatory mechanism of virus genome replication by NP. Stepwise cell-free replication reactions revealed that exogenously added NP free of RNA activates the viral polymerase during promoter escape while it is incapable of encapsidating the nascent cRNA. However, we found that a previously identified cellular protein, RAF-2p48/NPI-5/UAP56, facilitates replication reaction-coupled encapsidation as an NP molecular chaperone. These findings demonstrate that replication of the virus genome is followed by its encapsidation by NP in collaboration with its chaperone.
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