ATHB-17 is a class II HD-Zip transcription factor that acts as a transcriptional repressor containing an EAR-like motif, critical for modulating plant stress tolerance . It coordinates nuclear- and chloroplast-encoded photosynthetic genes (NEPGs and PEGs) under abiotic stress, enhancing stress resilience by:
Repressing NEPGs (e.g., FDA6, LHCA2, LHB1B1, LHB1B2, PSBO1) via direct promoter binding .
Activating PEGs (e.g., PSBA, PSBDC) indirectly through ATSIG5, a plastid sigma factor .
Balancing photosystem stoichiometry to protect photosynthesis machinery .
The antibody is primarily used for:
Chromatin Immunoprecipitation (ChIP): Validating ATHB-17’s direct binding to target gene promoters (e.g., ATSIG5) .
Subcellular Localization: Confirming nuclear localization via GFP fusion assays .
Protein Expression Analysis: Detecting HA-tagged ATHB-17 in overexpression lines .
Gene Type | Example Genes | Regulatory Role | Binding Confirmed? |
---|---|---|---|
NEPGs | FDA6, LHCA2 | Repression via direct binding | Yes |
PEGs | PSBA, PSBDC | Indirect activation | No |
Regulators | ATSIG5 | Direct activation | Yes |
Code | Source | Conjugate | Purity |
---|---|---|---|
CSB-YP854669DOA | Yeast | None | High |
CSB-EP854669DOA | E. coli | None | High |
CSB-BP854669DOA | Baculovirus | None | High |
Key Features:
Epitope Tags: HA-tagged variants enable detection using anti-HA antibodies .
Repression Domain: Truncated forms (e.g., ATHB17Δ113) lack the N-terminal repression domain, altering function .
Overexpression (OX) Lines: Show enhanced salt/drought tolerance, reduced oxidative damage, and increased photosynthetic capacity .
Knockout (KO) Mutants: Exhibit heightened stress sensitivity and dysregulated PEG/NEPG expression .
Condition | ATHB17 OX | ATHB17 KO |
---|---|---|
Salt Stress | Increased survival | Reduced survival |
Drought | Delayed wilting | Accelerated wilting |
ROS Levels | Lower H2O2 | Higher H2O2 |
Under stress, ATHB-17:
Binds NEPG promoters (e.g., LHB1B1) to suppress light-harvesting genes .
Activates ATSIG5, which upregulates PEGs to optimize photosystem repair .
Reduces chloroplast oxidative damage by balancing PSI/PSII ratios .