In Vitro Evidence That the Coat Protein of Alfalfa Mosaic Virus Plays a Direct Role in the Regulation of Plus and Minus RNA Synthesis: Implications for the Life Cycle of Alfalfa Mosaic Virus

• Published in: Virology (New York, N.Y.) Vol. 208; no. 2; pp. 583 - 589
• Main Authors: De Graaff, M., 'T Veld, M.R.Man In, Jaspars, E.M.J.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 20.04.1995
• Subjects: Alfalfa mosaic virus; Alfalfa mosaic virus - enzymology; Alfalfa mosaic virus - genetics; Alfalfa mosaic virus - physiology; arn; Capsid - metabolism; ciclo vital; cycle de developpement; experimentacion in vitro; experimentation in vitro; in vitro experimentation; life cycle; Models, Genetic; nicotiana; Nicotiana - virology; plant viruses; plantas transgenicas; plante transgenique; Plants, Toxic; proteinas; proteine; proteins; rna; RNA, Viral - biosynthesis; RNA-Dependent RNA Polymerase - isolation & purification; RNA-Dependent RNA Polymerase - metabolism; Templates, Genetic; transferasas; transferase; transferases; transgenic plants; Virion - enzymology; virus de las plantas; virus des vegetaux; Virus Replication - physiology
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1006/viro.1995.1189

The coat protein of alfalfa mosaic virus has both structural and regulating functions. The latter is evident from the fact that the genomic RNAs of the virus, although they are of messenger polarity, cannot start an infection cycle in the absence of coat protein. The reason could be that the coat protein is needed for viral RNA synthesis. Indeed, the coat protein has been found in tight association with the viral RNA polymerase (R. Quadt et al., 1991, Virology 182, 309-315). To investigate the role of the coat protein, if any, in viral RNA synthesis, we have isolated the viral RNA polymerase (RNA-dependent RNA polymerase, RdRp) from mock-inoculated tobacco plants transformed with cDNAs 1 and 2, known as P12 plants (P. E M Taschner et al., 1991, Virology 181,687-693), which express the nonstructural proteins P1 and P2. Such an enzyme (called M-RdRp) will contain the viral subunits P1 and P2 but not the coat protein. As a comparison we also isolated the RdRp from virion-inoculated P12 plants (C-RdRp). This enzyme will contain the coat protein. We found that both M-RdRp and CRdRp could synthesize minus RNA, showing that coat protein is not needed for minus-strand synthesis. In contrast, minusstrand synthesis by both enzymes was inhibited by coat protein. Plus-strand synthesis was unaffected by coat protein in the case of C-RdRp, but strongly stimulated by coat protein in the case of M-RdRp. These data might explain why infected cells, which do not produce coat protein, display a very low accumulation of viral plus-strand RNA. They also give a possible explanation for the noninfectious character of the genomes of alfafa mosaic virus and ilarviruses in the absence of coat protein. The fact that an active enzyme could be isolated from the same membrane fraction in infected and noninfected P12 plants shows that coat protein is not needed for assembly and targeting of the viral RNA polymerase.