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. 1983 May;46(2):614–619. doi: 10.1128/jvi.46.2.614-619.1983

Orientation of the Cleavage Map of the 200-Kilodalton Polypeptide Encoded by the Bottom-Component RNA of Cowpea Mosaic Virus

Rob Goldbach 1, Geertje Rezelman 1
PMCID: PMC255164  PMID: 16789243

Abstract

The genomic organization of the bottom-component RNA of cowpea mosaic virus was studied. In vivo, this RNA encodes at least eight different polypeptides of 170, 110, 87, 84, 60, 58, 32, and 4 kilodaltons (K), the last polypeptide representing the genome-bound protein VPg. In rabbit reticulocyte lysates, bottom-component RNA is translated into a 200K polypeptide which is then processed to give the 32 and 170K polypeptides also found in vivo. By pulse-labeling the 200K primary translation product, we now show that the 32 and 170K polypeptides are derived from the NH2-terminal and COOH-terminal parts of this polypeptide, respectively. Comparison of the proteolytic peptide patterns of 170K polypeptides synthesized in vitro and pulse-labeled at either the NH2-terminal or the COOH-terminal end with the patterns of the 170 and 110K polypeptides found in vivo demonstrates that the order within the 200K primary translation product of cowpea mosaic virus bottom-component RNA is as follows: NH2-32K polypeptide-58K polypeptide-VPg-24K polypeptide-87K polypeptide-COOH.

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Selected References

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