Sequence determination of the capsid protein gene and flanking regions of tobacco etch virus: Evidence for synthesis and processing of a polyprotein in potyvirus genome expression*

  1. Richard F. Allison,
  2. John C. Sorenson,
  3. Mary E. Kelly§,
  4. Frank B. Armstrong§, and
  5. William G. Dougherty,
  1. Department of Plant Pathology, North Carolina State University, Raleigh, NC 27695
  2. Department of Biochemistry, North Carolina State University, Raleigh, NC 27695
  3. Experimental Plant Genetics, The Upjohn Company, Kalamazoo, MI 49001

Abstract

The nucleotide sequence of the 3′-terminal portion of the tobacco etch virus (TEV) genome was determined. The 2324-nucleotide sequence represented approximately one-fourth of the TEV genome and included the capsid protein gene and flanking regions. An open reading frame of 2135 nucleotides and an untranslated region of 189 nucleotides adjacent to a polyadenylate tract were identified. The sequence began within an open reading frame, indicating that the initiation codon was upstream of the available sequence data. The sequence of the 20 NH2-terminal amino acids of the TEV capsid protein was established chemically. An identical amino acid sequence, predicted from the nucleotide sequence, was located, commencing at amino acid - 263. These data indicated that maturation of the capsid protein required a post-translational cleavage of a larger protein precursor, with a probable cleavage site between the amino acids glutamine and glycine.

Footnotes

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  • * Paper no. 9715 of The Journal Series of the North Carolina Agricultural Research Service, Raleigh, NC 27695-7601.

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