Abstract
The sequence of the first 71 nucleotides from the 3'-OH end of tobacco mosaic virus RNA has been determined. After total T1 ribonuclease digestion of the viral RNA, the oligonucleotide C-C-C-A-OH, which originates from the 3'-OH terminus of the RNA, may be readily detected by electrophoresis at pH 2.5 or pH 3.0; it is the only oligonucleotide that migrates toward the cathode at these pHs. This property has been used to screen the purified products of partial T1 ribonuclease digestion of tobacco mosaic virus RNA for the fragment originating from the 3'-end of the native molecule. The sequence of nucleotides in the 3'-terminal fragment, identified in this manner, was determined by radiochemical methods. The fragment contained 71 nucleotides; no abnormal bases could be detected. Although it has been reported that the 3'-end of tobacco mosaic virus RNA is a substrate for aminoacylation by the histidyl-tRNA synthetase of yeast or Escherichia coli, we were unable to fold the sequence into the cloverleaf structure characteristic of tRNAs.
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- Adams J. M., Jeppesen P. G., Sanger F., Barrell B. G. Nucleotide sequence from the coat protein cistron of R17 bacteriophage RNA. Nature. 1969 Sep 6;223(5210):1009–1014. doi: 10.1038/2231009a0. [DOI] [PubMed] [Google Scholar]
- Butler P. J., Klug A. Assembly of the particle of tobacco mosaic virus from RNA and disks of protein. Nat New Biol. 1971 Jan 13;229(2):47–50. doi: 10.1038/newbio229047a0. [DOI] [PubMed] [Google Scholar]
- Cory S., Adams J. M., Spahr P. F., Rensing U. Sequence of 51 nucleotides at the 3'-end of R17 bacteriophage RNA. J Mol Biol. 1972 Jan 14;63(1):41–56. doi: 10.1016/0022-2836(72)90520-7. [DOI] [PubMed] [Google Scholar]
- Fiers W., Contreras R., De Wachter R., Haegeman G., Merregaert J., Jou W. M., Vandenberghe A. Recent progress in the sequence determination of bacteriophage MS2 RNA. Biochimie. 1971;53(4):495–506. doi: 10.1016/s0300-9084(71)80167-0. [DOI] [PubMed] [Google Scholar]
- Glitz D. G., Bradley A., Fraenkel-Contrat H. Nucleotide sequences at the 5'-linked ends of viral ribonucleic acids. Biochim Biophys Acta. 1968 Jun 18;161(1):1–12. doi: 10.1016/0005-2787(68)90288-8. [DOI] [PubMed] [Google Scholar]
- Glitz D. G., Eichler D. Nucleotides at the 5'-linked ends of bromegrass mosaic virus RNA and its fragments. Biochim Biophys Acta. 1971 May 13;238(2):224–232. doi: 10.1016/0005-2787(71)90089-x. [DOI] [PubMed] [Google Scholar]
- Guilley H., Jonard G., Hirth L. A TMV RNA nucleotide sequence specifically recognized by TMV protein. Biochimie. 1974;56(1):181–185. doi: 10.1016/s0300-9084(74)80369-x. [DOI] [PubMed] [Google Scholar]
- Guilley H., Stussi C., Hirth L. Influence de la phosphodiestérase de rate de porc sur la reconstitution in vitro du virus de la mosaïque du tabac. C R Acad Sci Hebd Seances Acad Sci D. 1971 Feb 22;272(8):1181–1184. [PubMed] [Google Scholar]
- Hall T. C., Shih D. S., Kaesberg P. Enzyme-mediated binding of tyrosine to brome-mosaic-virus ribonucleic acid. Biochem J. 1972 Oct;129(4):969–976. doi: 10.1042/bj1290969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hiramaru M., Uchida T., Egami F. Ribonuclease preparation for the base analysis of polyribonucleotides. Anal Biochem. 1966 Oct;17(1):135–142. doi: 10.1016/0003-2697(66)90016-9. [DOI] [PubMed] [Google Scholar]
- Litvak S., Tarragó A., Tarragó-Litvak L., Allende J. E. Elongation factor-viral genome interaction dependent on the aminoacylation of TYMV and TMV RNAs. Nat New Biol. 1973 Jan 17;241(107):88–90. doi: 10.1038/newbio241088a0. [DOI] [PubMed] [Google Scholar]
- Mandeles S. Base sequence at the 5'-linked terminus of tobacco mosaic virus ribonucleic acid. J Biol Chem. 1967 Jul 10;242(13):3103–3107. [PubMed] [Google Scholar]
- Minson T., Darby G. Letter: 3'-Terminal oligonucleotide fragments of tobacco rattle virus ribonucleic acids. J Mol Biol. 1973 Jun 25;77(2):337–340. doi: 10.1016/0022-2836(73)90339-2. [DOI] [PubMed] [Google Scholar]
- Oberg B., Philipson L. Binding of histidine to tobacco mosaic virus RNA. Biochem Biophys Res Commun. 1972 Aug 21;48(4):927–932. doi: 10.1016/0006-291x(72)90697-3. [DOI] [PubMed] [Google Scholar]
- Pinck M., Yot P., Chapeville F., Duranton H. M. Enzymatic binding of valine to the 3' end of TYMV-RNA. Nature. 1970 Jun 6;226(5249):954–956. doi: 10.1038/226954a0. [DOI] [PubMed] [Google Scholar]
- Richards K. E., Guilley H., Jonard G., Hirth L. A specifically encapsidated fragment from the RNA of tobacco mosaic virus: sequence homology with the coat protein cistron. FEBS Lett. 1974 Jul 1;43(1):31–32. doi: 10.1016/0014-5793(74)81098-7. [DOI] [PubMed] [Google Scholar]
- Sanger F., Brownlee G. G., Barrell B. G. A two-dimensional fractionation procedure for radioactive nucleotides. J Mol Biol. 1965 Sep;13(2):373–398. doi: 10.1016/s0022-2836(65)80104-8. [DOI] [PubMed] [Google Scholar]
- Steinschneider A., Fraenkel-Conrat H. Studies of nucleotide sequences in tobacco mosaic virus ribonucleic acid. IV. Use of aniline in stepwise degradation. Biochemistry. 1966 Aug;5(8):2735–2743. doi: 10.1021/bi00872a034. [DOI] [PubMed] [Google Scholar]
- Thouvenel J. -C., Guilley H., Stussi C., Hirth L. Evidence for polar reconstitution of TMV. FEBS Lett. 1971 Aug 15;16(3):204–206. doi: 10.1016/0014-5793(71)80134-5. [DOI] [PubMed] [Google Scholar]
- Tinoco I., Jr, Borer P. N., Dengler B., Levin M. D., Uhlenbeck O. C., Crothers D. M., Bralla J. Improved estimation of secondary structure in ribonucleic acids. Nat New Biol. 1973 Nov 14;246(150):40–41. doi: 10.1038/newbio246040a0. [DOI] [PubMed] [Google Scholar]