EHMT2
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
REST
Gene Ontology Biological Process
- cardiac muscle cell myoblast differentiation [ISS]
- cellular response to drug [IMP]
- cellular response to electrical stimulus [IMP]
- cellular response to glucocorticoid stimulus [IDA]
- histone H4 deacetylation [IDA]
- negative regulation by host of viral transcription [IDA]
- negative regulation of aldosterone biosynthetic process [IMP]
- negative regulation of amniotic stem cell differentiation [IMP]
- negative regulation of calcium ion-dependent exocytosis [ISS]
- negative regulation of cell proliferation [IMP]
- negative regulation of cortisol biosynthetic process [IMP]
- negative regulation of dense core granule biogenesis [ISS]
- negative regulation of gene expression [IMP]
- negative regulation of insulin secretion [IMP]
- negative regulation of mesenchymal stem cell differentiation [IMP]
- negative regulation of neurogenesis [ISS]
- negative regulation of neuron differentiation [IMP]
- negative regulation of transcription from RNA polymerase II promoter [IDA, TAS]
- negative regulation of transcription, DNA-templated [IDA, IMP, NAS]
- positive regulation of apoptotic process [IMP]
- positive regulation of cysteine-type endopeptidase activity involved in apoptotic process [IMP]
- positive regulation of transcription, DNA-templated [IDA]
- potassium ion transmembrane transport [IMP]
- regulation of transcription, DNA-templated [NAS]
Gene Ontology Molecular Function- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription [IDA]
- chromatin binding [ISS]
- core promoter binding [IDA]
- core promoter sequence-specific DNA binding [IDA]
- outward rectifier potassium channel activity [IMP]
- protein binding [IPI]
- sequence-specific DNA binding transcription factor activity [IDA]
- transcription factor binding [IPI]
- transcription regulatory region DNA binding [IDA]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription [IDA]
- chromatin binding [ISS]
- core promoter binding [IDA]
- core promoter sequence-specific DNA binding [IDA]
- outward rectifier potassium channel activity [IMP]
- protein binding [IPI]
- sequence-specific DNA binding transcription factor activity [IDA]
- transcription factor binding [IPI]
- transcription regulatory region DNA binding [IDA]
Gene Ontology Cellular Component
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.
Publication
Localized domains of G9a-mediated histone methylation are required for silencing of neuronal genes.
Negative regulation of transcription is an important strategy in establishing and maintaining cell-specific gene expression patterns. Many neuronal genes are subject to active transcriptional repression outside the nervous system to establish neuronal specificity. NRSF/REST has been demonstrated to regulate at least 30 genes and contribute to their neuronal targeting by repressing transcription outside the nervous system. Further, human genome database ... [more]
Throughput
- Low Throughput
Additional Notes
- figure 3.
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| REST EHMT2 | 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 | 853090 |
Curated By
- BioGRID