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1 Department of Plant Pathology, University of Kentucky, Lexington, Kentucky 40546
2 Department of Biology, Indiana University of Pennsylvania, Indiana, Pennsylvania 15705
3 Department of Plant Pathology, Iowa State University, Ames, Iowa 50011
and4 Department of Plant Pathology, University of Minnesota, St Paul, Minnesota 55108, U.S.A.
The RNA of maize dwarf mosaic virus strain A (MDMV-A) was characterized and compared with that of strain B (MDMV-B). Glyoxal-treated MDMV-A RNA has an Mr of 3.32 x 106 measured in agarose gels, compared with that of MDMV-B which is 3.41 x 106 under the same conditions. MDMV-A RNA has a Tm of 50.7 °C and a hyperchromicity of 23.3%, which are higher than those reported for MDMV-B RNA. Translation products of both RNAs in a rabbit reticulocyte cell-free system ranged from 23K to 121K. Four major polypeptide products of 57K, 91K, 100K and 117K were produced by MDMV-A RNA-directed translation, and four major products of 39K, 55K, 86K and 121K by MDMV-B RNA. Protein profiles from the two RNAs were distinct including translation products that comigrated with authentic coat protein at 37K (MDMV-A) or 39K (MDMV-B) for each strain. Anti-virion sera immunoprecipitated polypeptide products from each strain. Distinct subsets of translation products were immunoprecipitated with antisera to tobacco etch virus 49K and 54K nuclear inclusion proteins. No cell-free translation products were recognized by antisera to potato virus Y (PVY) or tobacco vein mottling virus (TVMV) helper components or antisera to the cylindrical inclusion proteins of PVY or TVMV.
Keywords: MDMV, RNA, translation in vitro
Present address: Department of Plant, Soil, and Entomological Sciences, University of Idaho, Moscow, Idaho 83832, U.S.A.
Received 2 November 1988;
accepted 17 February 1989.
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