Publication | Open Access
Induction of a Highly Specific Antiviral State in Transgenic Plants: Implications for Regulation of Gene Expression and Virus Resistance.
726
Citations
35
References
1993
Year
EngineeringGeneticsCoat ProteinPlant PathologyMolecular GeneticsPlant VirologyPlant-virus InteractionVirus GenePlant VirusVirus ResistanceVirologySteady State LevelsGene ExpressionBiologyTransgenic PlantsDevelopmental BiologyGenetic EngineeringTransgenic Tobacco PlantsMedicineViral ImmunityPlant Physiology
The study investigates how transgenic tobacco plants develop a virus‑specific resistant state after TEV infection. The authors propose that a cytoplasmic activity targeting specific RNA sequences mediates this resistant state and the reduced accumulation of transgene transcripts. Transgenic tobacco initially infected with TEV recovers after 3–5 weeks, forming new symptom‑free tissue that is resistant to TEV but not to PVY, with transgene mRNA levels reduced 12–22‑fold while transcription rates remain unchanged.
Transgenic tobacco plants expressing either a full-length form of the tobacco etch virus (TEV) coat protein or a form truncated at the N terminus of the TEV coat protein were initially susceptible to TEV infection, and typical systemic symptoms developed. However, 3 to 5 weeks after a TEV infection was established, transgenic plants "recovered" from the TEV infection, and new stem and leaf tissue emerged symptom and virus free. A TEV-resistant state was induced in the recovered tissue. The resistance was virus specific. Recovered plant tissue could not be infected with TEV, but was susceptible to the closely related virus, potato virus Y. The resistance phenotype was functional at the single-cell level because protoplasts from recovered transgenic tissue did not support TEV replication. Surprisingly, steady state transgene mRNA levels in recovered tissue were 12-to 22-fold less than transgene mRNA levels in uninoculated transgenic tissue of the same developmental stage. However, nuclear run-off studies suggested that transgene transcription rates in recovered and uninoculated plants were similar. We propose that the resistant state and reduced steady state levels of transgene transcript accumulation are mediated at the cellular level by a cytoplasmic activity that targets specific RNA sequences for inactivation.
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