Abstract
Evidence for capped poly(A) leaders of variable lengths located immediately upstream of the translation initiation codon was obtained by direct analyses of a major late mRNA species. A decapping-recapping method was used to specifically substitute a radioactively labeled phosphate for an unlabeled one within the cap structure. RNase H-susceptible sites were made by hybridizing synthetic oligodeoxyribonucleotides to the mRNA encoding a late major structural protein of 11 kilodaltons. Sequences of the type m7G(5')pppAmp (Ap)(n)UpG..., where n varies from a few to more than 40 nucleotides, were deduced by analysis of the length and sequence of RNase H, RNase, T1, and RNase U2 digestion products.
Original language | English |
---|---|
Pages (from-to) | 226-232 |
Number of pages | 7 |
Journal | Journal of virology |
Volume | 63 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1989 |
ASJC Scopus subject areas
- Microbiology
- Immunology
- Insect Science
- Virology