Identification, cloning, and R-Loop mapping of the polyhedrin gene from the multicapsid nuclear polyhedrosis virus of Orgyia pseudotsugata

• Published in: Virology (New York, N.Y.) Vol. 121; no. 1; pp. 51 - 60
• Main Authors: Rohrmann, George F., Leisy, Douglas J., Chow, Kuan-Chih, Pearson, George D., Beaudreau, George S.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.1982
• Subjects: nuclear polyhedrosis virus
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1016/0042-6822(82)90117-9

Polyadenylated RNA was isolated from Orgyia pseudotsugata larvae 8–10 days postinfection with the multicapsid nuclear polyhedrosis virus. This RNA was centrifuged through a sucrose gradient and fractions enriched for polyhedrin mRNA were identified by in vitro translation. Complementary DNA made to this RNA hybridized predominantly to a 5-kb fragment of XhoI-digested viral DNA. This fragment was cloned into the plasmid pACYC177 and mapped with restriction endonucleases. A SalI subclone with a 2.5-kb insert derived from the cloned XhoI fragment was found to select by hybridization only polyhedrin mRNA as determined by the size of the in vitro translation product and its precipitation by anti-polyhedrin antibodies. The orientation of the polyhedrin gene and the region of the insert encoding the N terminus of the polyhedrin protein were determined by DNA sequencing. R-Loop mapping indicated polyhedrin mRNA is 980 ± 75 bases long and contains about 250 nucleotides not represented in the final protein. The polyhedrin gene had no observable intervening sequences.