Mapping of the large RNA genome segment of infectious pancreatic necrosis virus by hybrid arrested translation

Eva Nagy, Roy Duncan, Peter Krell, Peter Dobos

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37 Citations (Scopus)

Abstract

Segment A, the larger dsRNA segment of IPNV which encodes three of the four virus-coded polypeptides (preVP2, VP3, and NS) was cloned and physically mapped. The plus and minus RNA strands of the virus genome were separated and the A+ and B+ RNA strands were identified. A nested set of cDNA subclones, coterminal with the 5′ end of A+ RNA, were used in hybrid arrested translation experiments. Hybrid arrest conditions which blocked the 5′ two-thirds of A+ RNA allowed the in vitro synthesis of only VP3, while hybridization of the RNA to cDNA representing the 5′ half of A+ RNA allowed the synthesis of both NS and VP3 but not of preVP2. In vitro translation of A+ RNA yielded all three polypeptides. It is, therefore, concluded that the order of the three polypeptides on A+ RNA is 5′-preVP2-NS-VP3-3′. These results imply that internal initiation of translation could take place on the RNA at least in vitro at sites located hundreds of nucleotides downstream from the first in-phase AUG codon near the 5′ end.

Original languageEnglish
Pages (from-to)211-217
Number of pages7
JournalVirology
Volume158
Issue number1
DOIs
Publication statusPublished - May 1987
Externally publishedYes

Bibliographical note

Funding Information:
This investigation was supported by the National Science and Engineering Research Council of Canada. We are grateful to Mary K. Homonylo and William R. Lawrence for their excellent technical as-

ASJC Scopus Subject Areas

  • Virology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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Nagy, E., Duncan, R., Krell, P., & Dobos, P. (1987). Mapping of the large RNA genome segment of infectious pancreatic necrosis virus by hybrid arrested translation. Virology, 158(1), 211-217. https://doi.org/10.1016/0042-6822(87)90255-8