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Nucleic Acids Research, 1980, Vol. 8, No. 2 337-350
© 1980


Article

Assignment of reovirus mRNA ribosome binding sites to virion genome segments by nucleotide sequence analyses

Edward Darzynkiewicz* and Aaron J. Shatkin

Roche Institute of Molecular Biology, Nutley, NJ 07110, USA

Received August 21, 1979.

All ten reovirus genome RNA segments were radiolabeled at their 3'-termini by incubation with RNA ligase and 32pCp. The extent of radiolabeling was similar for each of the double-stranded RNAs in the genome segment mixture. Radioactivity was equally distributed between the separated plus and minus strands indicating that the 5'-cap in plus strands did not block 3'-end-labeling of minus strands. The 3'-termini of the four S and three M segments included the common sequences: ...U-A-G-C in minus strands and ...U-C-A-U-C in plus strands. By comparing the minus strand 3'-sequences with 5'— sequences of reovirus mRNAs, small-size genome segments S2, S3 and S4 were correlated with the previously sequenced initiation fragments s46, s45 and s54 derived from small class mRNAs. Medium-size genome segments Ml, M2 and M3 similarly were correlated with fragments m30, m52 and m44, respectively. The N-termlnal amino acid sequences deduced from the mRNA nucleotide sequences can now be assigned to the nascent chains of particular reovirus proteins.


*Permanent address: University of Warsaw, Institute, Institute of Experimental Physics, Department of Biophysics, Warsaw, poland.


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