Claim · model-written summary
Electrophoretic mobility shift assays confirmed direct binding of CsBES1-14 to cis-elements in the CsCOR413 promoter.
- Taxon
- tea plantt0
- Gene
- CsBES1-14e0
- Outcome
- direct binding of CsBES1-14 to specific cis-elements in the CsCOR413 promotere0
Not reportedMaterialCompoundOrgan / stageInteractorInteractor roleSecond interactorSecond interactor roleTreatmentComparatorSettingDirectionValueQualifier
Verbatim
t0“cold resistance in tea plant”
e0“electrophoretic mobility shift assays confirmed the direct binding of CsBES1-14 to specific cis-elements in the CsCOR413 promoter”
Title
Chao Wang; Jinyu Yang; Yichen Zhao; et al. Horticulture Research 2026. doi:10.1093/hr/uhag098
Other claims from this paper (10)
- Observation The CsBES1-14 gene was cloned and identified from the tea plant transcriptome database.
- Observation Biochemical analyses identified CsBES1-14 as a nuclear-localized transcriptional activator.
- Intervention effect Brassinosteroid induced CsBES1-14 expression.
- Intervention effect Low temperature induced CsBES1-14 expression.
- Intervention effect Arabidopsis thaliana plants overexpressing CsBES1-14 showed increased chilling tolerance.
- Intervention effect Arabidopsis thaliana plants overexpressing CsBES1-14 showed promoted root growth.
- Intervention effect Arabidopsis thaliana plants overexpressing CsBES1-14 showed increased expression of cold responsive genes.
- Intervention effect Silencing CsBES1-14 by VIGS in tea plant notably impaired cold tolerance.
- Observation Yeast one-hybrid screening identified CsCOR413 as a downstream target of CsBES1-14.
- Mechanism Brassinazole application and VIGS experiments verified that the ICE-CBF cold response pathway can regulate CsCOR413.