GLI1
Gene Ontology Biological Process
- cerebellar cortex morphogenesis [IGI]
- dorsal/ventral pattern formation [IGI]
- epidermal cell differentiation [ISO]
- lung development [IGI]
- negative regulation of canonical Wnt signaling pathway [ISO]
- notochord regression [IGI]
- osteoblast differentiation [ISO]
- pituitary gland development [IGI]
- positive regulation of DNA replication [ISO]
- positive regulation of cell proliferation [ISO]
- positive regulation of smoothened signaling pathway [ISO]
- positive regulation of transcription from RNA polymerase II promoter [IDA, ISO]
- positive regulation of transcription, DNA-templated [IDA, IMP, ISO]
- proximal/distal pattern formation [IGI]
- signal transduction [TAS]
- smoothened signaling pathway [IDA, IGI, ISO]
- smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation [IGI]
- spermatogenesis [IDA]
- transcription from RNA polymerase II promoter [IDA]
- ventral midline development [IGI]
Gene Ontology Molecular Function
SUFU
Gene Ontology Biological Process
- cytoplasmic sequestering of transcription factor [IGI]
- determination of left/right symmetry [IMP]
- heart looping [IMP]
- negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process [IGI]
- negative regulation of smoothened signaling pathway [IDA, IMP]
- negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning [IMP]
- negative regulation of transcription from RNA polymerase II promoter [IDA, ISO]
- neural tube closure [IMP]
- skin development [IMP]
- smoothened signaling pathway involved in spinal cord motor neuron cell fate specification [IMP]
- smoothened signaling pathway involved in ventral spinal cord interneuron specification [IMP]
- spinal cord dorsal/ventral patterning [IMP]
Gene Ontology Molecular Function
Affinity Capture-MS
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.
Publication
Loss of the tumor suppressor Snf5 leads to aberrant activation of the Hedgehog-Gli pathway.
Aberrant activation of the Hedgehog (Hh) pathway can drive tumorigenesis. To investigate the mechanism by which glioma-associated oncogene family zinc finger-1 (GLI1), a crucial effector of Hh signaling, regulates Hh pathway activation, we searched for GLI1-interacting proteins. We report that the chromatin remodeling protein SNF5 (encoded by SMARCB1, hereafter called SNF5), which is inactivated in human malignant rhabdoid tumors (MRTs), ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| GLI1 SUFU | Affinity Capture-Luminescence Affinity Capture-Luminescence An interaction is inferred when a bait protein, tagged with luciferase, is enzymatically detected in immunoprecipitates of the prey protein as light emission. The prey protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag. | Low | - | BioGRID | 2932368 | |
| SUFU GLI1 | Affinity Capture-Western Affinity Capture-Western An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | - | |
| SUFU GLI1 | Affinity Capture-Western Affinity Capture-Western An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | - | |
| GLI1 SUFU | Affinity Capture-Western Affinity Capture-Western An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | - |
Curated By
- BioGRID