The satellite RNA of tobacco ringspot virus, abbreviated STobRV RNA, has startling chemical and biological properties. When it is coinoculated with tobacco ringspot virus, STobRV RNA reduces the extent of virus replication and protects the plant from the most severe effects of the virus. STobRV RNA occurs in repetitive sequence, multimeric forms as well as the 359 nucleotide residue """"""""monomeric"""""""" form. Dimeric and trimeric forms of the RNA from virus particles spontaneously cleave to produce authentic, biologically active monomeric STobRV RNA in a reaction that may reflect a part of the replication cycle in vivo. This autolytic processing reaction clearly is non-enzymic beacuse of its resistance to proteinase treatments and because in vitro transcripts of cloned STobRV RNA sequences also spontaneously cleave. The reaction occurs even with RNAs that have most of the STobRV RNA sequence deleted. We will determine what is the minimum, or close to the minimum, polyribonucleotide chain that is sufficient for autolysis. From the corresponding cloned sequences in plasmids we will produce abundant in vitro transcripts. The two RNA products of the autolytic reaction will be probed, both separately and together, with structure sensitive endonucleases. We will attempt to grow crystals of the RNAs, separately and together, for future X-ray diffraction studies. Finally, the nucleotide sequences will be altered to determine their contributions to the autolytic reaction. We will examine both naturally occurring nucleotide substitutions, from STobRV RNA strains, an induced mutations. Various selection systems for mutants are proposed. Although no strict analogue of the plant virus small satellite RNAs has been discovered in association with animal or human viruses, we believe that the satellite RNA phenomenon deserves attention because of its potential for understanding how virus increase can be controlled. Autolytic RNA demands investigation not only on these grounds but also bacause of its unusual chemical and biological properties.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM037627-01
Application #
3293048
Study Section
Virology Study Section (VR)
Project Start
1986-12-01
Project End
1989-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
1
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of California Davis
Department
Type
Earth Sciences/Resources
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Van Tol, H; Buzayan, J M; Bruening, G (1991) Evidence for spontaneous circle formation in the replication of the satellite RNA of tobacco ringspot virus. Virology 180:23-30
Bruening, G; Passmore, B K; van Tol, H et al. (1991) Replication of a plant virus satellite RNA: evidence favors transcription of circular templates of both polarities. Mol Plant Microbe Interact 4:219-25
Feldstein, P A; Buzayan, J M; van Tol, H et al. (1990) Specific association between an endoribonucleolytic sequence from a satellite RNA and a substrate analogue containing a 2'-5' phosphodiester. Proc Natl Acad Sci U S A 87:2623-7
van Tol, H; Buzayan, J M; Feldstein, P A et al. (1990) Two autolytic processing reactions of a satellite RNA proceed with inversion of configuration. Nucleic Acids Res 18:1971-5
Buzayan, J M; van Tol, H; Feldstein, P A et al. (1990) Identification of a non-junction phosphodiester that influences an autolytic processing reaction of RNA. Nucleic Acids Res 18:4447-51
Feldstein, P A; Buzayan, J M; Bruening, G (1989) Two sequences participating in the autolytic processing of satellite tobacco ringspot virus complementary RNA. Gene 82:53-61
Buzayan, J M; Feldstein, P A; Segrelles, C et al. (1988) Autolytic processing of a phosphorothioate diester bond. Nucleic Acids Res 16:4009-23
Buzayan, J M; Feldstein, P A; Bruening, G et al. (1988) RNA mediated formation of a phosphorothioate diester bond. Biochem Biophys Res Commun 156:340-7