Skip to main content
The Plant Cell logoLink to The Plant Cell
. 1989 Dec;1(12):1165–1173. doi: 10.1105/tpc.1.12.1165

Determination of sequence and structural requirements for pathogenicity of a cucumber mosaic virus satellite RNA (Y-satRNA).

C Masuta 1, Y Takanami 1
PMCID: PMC159852  PMID: 2485234

Abstract

We describe the use of biologically active cDNA clones to investigate genetic determinants of a satellite RNA that modulates symptoms normally induced by its helper virus, cucumber mosaic virus (CMV). For this purpose, we have investigated a CMV satellite RNA (Y-satRNA) that induces bright yellow symptoms on tobacco and necrosis on tomato. To determine the pathogenicity-modulating domain of Y-satRNA, several insertion and deletion mutants were created by using various restriction sites in the cDNA of Y-satRNA, and RNA transcripts derived from the clones were mixed with CMV and used to inoculate plants. Although the satellite RNA was able to tolerate small insertions (as much as 4 bases at present), small deletions were deleterious, indicating that the sequence requirements for viability of the satellite RNA are relatively inflexible. Biological activity assays of chimeric satellite RNAs between Y-satRNA and a non-necrogenic satellite RNA, T73-satRNA, suggested that only two (or at least one of two) specific bases (positions 318 and 325) in the 3' region direct the necrogenic property of Y-satRNA. Sequences involved in production of yellow symptoms were investigated by constructing chimeras between Y-sat cDNA and cDNA of a satellite RNA designated S19-satRNA. S19-satRNA has considerable homology to Y-satRNA but does not elicit yellow symptoms on tobacco. Chimeric clones were constructed by using a BstXI site that cuts within a stable secondary structure in the region between positions 100 and 200 (region Y). The results of infectivity tests with RNA transcripts suggest that formation of a secondary structure in region Y may be involved in induction of yellow symptoms as well as viability of Y-satRNA.

Full Text

The Full Text of this article is available as a PDF (1.5 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bourque D. P., Hagiladi A., Naylor A. W. A method for extracting intact chloroplast and cytoplasmic ribosomal RNA from leaves. Biochem Biophys Res Commun. 1973 Apr 16;51(4):993–999. doi: 10.1016/0006-291x(73)90025-9. [DOI] [PubMed] [Google Scholar]
  2. Chen E. Y., Seeburg P. H. Supercoil sequencing: a fast and simple method for sequencing plasmid DNA. DNA. 1985 Apr;4(2):165–170. doi: 10.1089/dna.1985.4.165. [DOI] [PubMed] [Google Scholar]
  3. Hidaka S., Hanada K., Ishikawa K., Miura K. Complete nucleotide sequence of two new satellite RNAs associated with cucumber mosaic virus. Virology. 1988 Jun;164(2):326–333. doi: 10.1016/0042-6822(88)90545-4. [DOI] [PubMed] [Google Scholar]
  4. Kaper J. M., Tousignant M. E., Steen M. T. Cucumber mosaic virus-associated RNA 5. XI. Comparison of 14 CARNA 5 variants relates ability to induce tomato necrosis to a conserved nucleotide sequence. Virology. 1988 Apr;163(2):284–292. doi: 10.1016/0042-6822(88)90268-1. [DOI] [PubMed] [Google Scholar]
  5. Kaper J. M., Waterworth H. E. Cucumber mosaic virus associated RNA 5: causal agent for tomato necrosis. Science. 1977 Apr 22;196(4288):429–431. doi: 10.1126/science.196.4288.429. [DOI] [PubMed] [Google Scholar]
  6. Palukaitis P. Pathogenicity regulation by satellite RNAs of cucumber mosaic virus: minor nucleotide sequence changes alter host responses. Mol Plant Microbe Interact. 1988 Apr;1(4):175–181. doi: 10.1094/mpmi-1-175. [DOI] [PubMed] [Google Scholar]
  7. Schnölzer M., Haas B., Raam K., Hofmann H., Sänger H. L. Correlation between structure and pathogenicity of potato spindle tuber viroid (PSTV). EMBO J. 1985 Sep;4(9):2181–2190. doi: 10.1002/j.1460-2075.1985.tb03913.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Zuker M., Stiegler P. Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information. Nucleic Acids Res. 1981 Jan 10;9(1):133–148. doi: 10.1093/nar/9.1.133. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Plant Cell are provided here courtesy of Oxford University Press

RESOURCES