PKL
Gene Ontology Biological Process
- cell proliferation [IMP]
- chromatin modification [ISS]
- cytokinin-activated signaling pathway [IMP]
- negative regulation of abscisic acid-activated signaling pathway [IMP]
- negative regulation of transcription, DNA-templated [IMP]
- regulation of lateral root development [IMP]
- response to auxin [IMP]
- response to gibberellin [IMP]
- root development [IMP]
Gene Ontology Molecular Function
HY5
Gene Ontology Biological Process
- gibberellic acid mediated signaling pathway [IMP]
- photomorphogenesis [TAS]
- positive regulation of anthocyanin metabolic process [IMP]
- positive regulation of circadian rhythm [IMP]
- red or far-red light signaling pathway [IMP]
- regulation of photomorphogenesis [IMP]
- regulation of transcription, DNA-templated [ISS, TAS]
- response to UV-B [IEP, IGI, IMP]
- response to abscisic acid [IMP]
- response to far red light [IEP]
- response to karrikin [IEP]
- response to red light [IEP]
Gene Ontology Molecular Function
Two-hybrid
Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation.
Publication
Arabidopsis Chromatin Remodeling Factor PICKLE Interacts with Transcription Factor HY5 to Regulate Hypocotyl Cell Elongation.
Photomorphogenesis is a critical plant developmental process that involves light-mediated transcriptome changes, histone modifications, and inhibition of hypocotyl growth. However, the chromatin-based regulatory mechanism underlying this process remains largely unknown. Here, we identify ENHANCED PHOTOMORPHOGENIC1 (EPP1), previously known as PICKLE (PKL), an ATP-dependent chromatin remodeling factor of the chromodomain/helicase/DNA binding family, as a repressor of photomorphogenesis in Arabidopsis thaliana. We ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| PKL HY5 | PCA PCA A Protein-Fragment Complementation Assay (PCA) is a protein-protein interaction assay in which a bait protein is expressed as fusion to one of the either N- or C- terminal peptide fragments of a reporter protein and prey protein is expressed as fusion to the complementary N- or C- terminal fragment of the same reporter protein. Interaction of bait and prey proteins bring together complementary fragments, which can then fold into an active reporter, e.g. the split-ubiquitin assay. | Low | - | BioGRID | - | |
| PKL HY5 | Reconstituted Complex Reconstituted Complex An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator. | Low | - | BioGRID | - |
Curated By
- BioGRID