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 language | English |
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Pages (from-to) | 211-217 |
Number of pages | 7 |
Journal | Virology |
Volume | 158 |
Issue number | 1 |
DOIs | |
Publication status | Published - May 1987 |
Externally published | Yes |
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