Formation of brome mosaic virus RNA-dependent RNA polymerase in yeast requires coexpression of viral proteins and viral RNA

• Published in: Proceedings of the National Academy of Sciences - PNAS 1995-05, Vol.92 (11), p.4892-4896
• Main Authors: Quadt, R. (University of Wisconsin-Madison, Madison, WI.), Ishikawa, M, Janda, M, Ahlquist, P
• Format: Article
• Language: English
• Subjects: ARN; Biochemistry; brome mosaic virus; BROMOVIRUS; Bromovirus - enzymology; Bromovirus - physiology; Capsid proteins; Cell extracts; Cloning, Molecular; EXPRESION GENICA; EXPRESSION DES GENES; Gene Deletion; Genes, Viral; GENOMAS; GENOME; Hordeum - virology; Plants - virology; Plasmids; PROTEINAS; PROTEINE; Proteins; Ribonucleic acid; RNA; RNA Replicase - biosynthesis; RNA, Double-Stranded - biosynthesis; RNA, Viral - biosynthesis; SACCHAROMYCES CEREVISIAE; Saccharomyces cerevisiae - metabolism; Templates, Genetic; TRANSFERASAS; TRANSFERASE; TRANSFORMACION GENETICA; TRANSFORMATION GENETIQUE; Viral Proteins - biosynthesis; Viral RNA; Virions; Virology; VIRUS; VIRUS DE LAS PLANTAS; VIRUS DES VEGETAUX; Virus Replication; Viruses; Yeast; Yeasts
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.92.11.4892

In this report we show that yeast expressing brome mosaic virus (BMV) replication proteins la and 2a and replicating a BMV RNA3 derivative can be extracted to yield a template-dependent BMV RNA-dependent RNA polymerase (RdRp) able to synthesize (-)-strand RNA from BMV (+)-strand RNA templates added in vitro. This virus-specific yeast-derived RdRp mirrored the template selectivity and other characteristics of RdRp from BMV-infected plants. Equivalent extracts from yeast expressing 1a and 2a but lacking RNA3 contained normal amounts of 1a and 2a but had no RdRp activity on BMV RNAs added in vitro To determine which RNA3 sequences were required in vivo to yield RdRp activity, we tested deletions throughout RNA3, including the 5', 3', and intercistronic noncoding regions, which contain the cis-acting elements required for RNA3 replication in vivo. RdRp activity was obtained only from cells expressing 1a, 2a, and RNA3 derivatives retaining both 3' and intercistronic noncoding sequences. Strong correlation between extracted RdRp activity and BMV (-)-strand RNA accumulation in vivo was found for all RNA3 derivatives tested. Thus, extractable in vitro RdRp activity paralleled formation of a complex capable of viral RNA synthesis in vivo The results suggest that assembly of active RdRp requires not only viral proteins but also viral RNA, either to directly contribute some nontemplate function or to recruit essential host factors into the RdRp complex and that sequences at both the 3'-terminal initiation site and distant internal sites of RNA3 templates may participate in RdRp assembly and initiation of (-)-strand synthesis