An influenza virus replicon system in yeast identified Tat-SF1 as a stimulatory host factor for viral RNA synthesis
- Tadasuke Naito*,
- Yoshihiko Kiyasu*,
- Kenji Sugiyama*,
- Ayumi Kimura*,†,
- Ryosuke Nakano‡,
- Akio Matsukage†, and
- Kyosuke Nagata*,§
- *Department of Infection Biology, Graduate School of Comprehensive Human Sciences and Institute of Basic Medical Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8575, Japan;
- †Department of Chemical and Biological Sciences, Faculty of Science, Graduate School of Science, Japan Women's University, 2-8-1 Mejirodai, Bunkyo-ku, Tokyo 112-8681, Japan; and
- ‡Tokyo Research Laboratories, Kyowa Hakko Kogyo Company, Tokyo 194-8533, Japan
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Edited by Robert A. Lamb, Northwestern University, Evanston, IL, and approved October 3, 2007 (received for review June 22, 2007)
Abstract
Influenza viruses infect vertebrates, including mammals and birds. Influenza virus reverse-genetics systems facilitate the study of the structure and function of viral factors. In contrast, less is known about host factors involved in the replication process. Here, we developed a replication and transcription system of the negative-strand RNA genome of the influenza virus in Saccharomyces cerevisiae, which depends on viral RNAs, viral RNA polymerases, and nucleoprotein (NP). Disruption of SUB2 encoding an orthologue of human RAF-2p48/UAP56, a previously identified viral RNA synthesis stimulatory host factor, resulted in reduction of the viral RNA synthesis rate. Using a genome-wide set of yeast single-gene deletion strains, we found several host factor candidates affecting viral RNA synthesis. We found that among them, Tat-SF1, a mammalian homologue of yeast CUS2, was a stimulatory host factor in influenza virus RNA synthesis. Tat-SF1 interacted with free NP, but not with NP associated with RNA, and facilitated formation of RNA-NP complexes. These results suggest that Tat-SF1 may function as a molecular chaperone for NP, as does RAF-2p48/UAP56. This system has proven useful for further studies on the mechanism of influenza virus genome replication and transcription.
Footnotes
- §To whom correspondence should be addressed. E-mail: knagata{at}md.tsukuba.ac.jp
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Author contributions: T.N. and K.N. designed research; T.N., Y.K., K.S., A.K., and R.N. performed research; K.S. contributed new reagents/analytic tools; T.N., A.M., and K.N. analyzed data; and T.N. and K.N. wrote the paper.
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The authors declare no conflict of interest.
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This article is a PNAS Direct Submission.
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This article contains supporting information online at www.pnas.org/cgi/content/full/0705856104/DC1.
- © 2007 by The National Academy of Sciences of the USA





