Claim · model-written summary
INA induced PR-1a in wild-type and reporter tobacco.
- Taxon
- tobacco
Nicotiana tabacume1 - Treatment
- 2,6-dichloro-isonicotinic acid (INA)e0
- Outcome
- express PR-1ae0
Not reportedMaterialGeneCompoundOrgan / stageInteractorInteractor roleSecond interactorSecond interactor roleComparatorSettingDirectionValueQualifier
Organisms pictured · Representative pictures of the matched species, not figures from the paper.
Verbatim
e0“Wild-type and PR-1a-GUS-transformed plants express PR-1a following challenge with Pseudomonas syringae pathovar syringae, SA or 2,6-dichloro-isonicotinic acid (INA).”
e1“PR proteins in tobacco”
Title
Yong‐Mei Bi; Paul Kenton; Luis Mur; et al. The Plant Journal 1995. doi:10.1046/j.1365-313x.1995.08020235.x
Other claims from this paper (14)
- Intervention effect Pathogen challenge induced PR-1a in wild-type and PR-1a-GUS tobacco.
- Intervention effect SA induced PR-1a in wild-type and reporter tobacco.
- Intervention effect SA failed to induce PR-1a in SH-L tobacco.
- Intervention effect INA induced PR-1a in SH-L tobacco.
- Intervention effect H2O2 weakly induced PR-1a in wild-type tobacco relative to SA.
- Intervention effect 3-AT weakly induced PR-1a in wild-type tobacco relative to SA.
- Intervention effect H2O2 did not induce PR-1a in SH-L tobacco.
- Intervention effect 3-AT did not induce PR-1a in SH-L tobacco.
- Mechanism The effects of peroxide and 3-AT were interpreted as depending on SA accumulation.
- Intervention effect Catalase activity showed no significant change after P. syringae infection.
- Intervention effect In vitro SA inhibited tobacco catalase only after preincubation and above 250 microM.
- Intervention effect Leaf disks given 1 mM SA accumulated SA and efficiently induced PR-1a without apparent catalase inhibition.
- Intervention effect SA-treated leaf disks showed no apparent catalase inhibition.
- Intervention effect PR-1a and AoPR-1 were relatively insensitive to 3-AT.