YY1
Gene Ontology Biological Process
- RNA localization [IMP]
- anterior/posterior pattern specification [IGI, IMP]
- camera-type eye morphogenesis [IGI]
- cellular response to DNA damage stimulus [IMP, ISO]
- cellular response to UV [ISO]
- cellular response to interleukin-1 [ISO]
- chromosome organization [IMP]
- double-strand break repair via homologous recombination [ISO]
- negative regulation of transcription from RNA polymerase II promoter [IDA, ISO]
- positive regulation of gene expression [IDA]
- positive regulation of transcription from RNA polymerase II promoter [ISO]
- regulation of transcription, DNA-templated [IDA, ISO]
- response to UV-C [IMP, ISO]
- spermatogenesis [IMP]
- transcription from RNA polymerase II promoter [IDA]
Gene Ontology Molecular Function- DNA binding [IDA, ISO]
- RNA binding [ISO]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription [IDA]
- four-way junction DNA binding [ISO]
- histone deacetylase binding [ISO]
- protein binding [IPI]
- sequence-specific DNA binding [ISO]
- sequence-specific DNA binding transcription factor activity [IDA]
- transcription regulatory region DNA binding [ISO]
- DNA binding [IDA, ISO]
- RNA binding [ISO]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription [IDA]
- four-way junction DNA binding [ISO]
- histone deacetylase binding [ISO]
- protein binding [IPI]
- sequence-specific DNA binding [ISO]
- sequence-specific DNA binding transcription factor activity [IDA]
- transcription regulatory region DNA binding [ISO]
Gene Ontology Cellular Component
MTOR
Gene Ontology Biological Process
- TOR signaling [ISO]
- cell growth [ISO]
- cell projection organization [IMP, ISO]
- cellular response to hypoxia [IDA]
- cellular response to nutrient levels [IDA]
- double-strand break repair via homologous recombination [IBA]
- germ cell development [IDA]
- negative regulation of NFAT protein import into nucleus [IMP]
- negative regulation of autophagy [IMP]
- negative regulation of cell size [IGI, ISO]
- negative regulation of macroautophagy [IMP]
- peptidyl-serine phosphorylation [IMP, ISO]
- peptidyl-threonine phosphorylation [IDA]
- phosphorylation [ISO]
- positive regulation of actin filament polymerization [IDA, IMP]
- positive regulation of endothelial cell proliferation [ISO]
- positive regulation of gene expression [ISO]
- positive regulation of lamellipodium assembly [IDA]
- positive regulation of lipid biosynthetic process [ISO]
- positive regulation of myotube differentiation [IGI]
- positive regulation of peptidyl-tyrosine phosphorylation [IMP]
- positive regulation of protein kinase B signaling [ISO]
- positive regulation of protein phosphorylation [ISO]
- positive regulation of stress fiber assembly [IDA]
- positive regulation of transcription from RNA polymerase III promoter [ISO]
- positive regulation of translation [ISO]
- protein autophosphorylation [ISO]
- protein phosphorylation [ISO]
- regulation of Rac GTPase activity [IMP]
- regulation of actin cytoskeleton organization [ISO]
- regulation of carbohydrate metabolic process [ISO]
- regulation of carbohydrate utilization [ISO]
- regulation of fatty acid beta-oxidation [ISO]
- regulation of glycogen biosynthetic process [ISO]
- regulation of myelination [IMP]
- regulation of protein kinase activity [IGI]
- regulation of response to food [ISO]
- response to amino acid [IDA, ISO]
- response to insulin [IDA]
- response to stress [ISO]
- ruffle organization [IDA]
Gene Ontology Molecular Function- RNA polymerase III type 1 promoter DNA binding [ISO]
- RNA polymerase III type 2 promoter DNA binding [ISO]
- RNA polymerase III type 3 promoter DNA binding [ISO]
- TFIIIC-class transcription factor binding [ISO]
- kinase activity [ISO]
- phosphoprotein binding [ISO]
- protein binding [IPI]
- protein dimerization activity [IBA]
- protein domain specific binding [ISO]
- protein serine/threonine kinase activity [IDA, ISO]
- ribosome binding [IDA]
- RNA polymerase III type 1 promoter DNA binding [ISO]
- RNA polymerase III type 2 promoter DNA binding [ISO]
- RNA polymerase III type 3 promoter DNA binding [ISO]
- TFIIIC-class transcription factor binding [ISO]
- kinase activity [ISO]
- phosphoprotein binding [ISO]
- protein binding [IPI]
- protein dimerization activity [IBA]
- protein domain specific binding [ISO]
- protein serine/threonine kinase activity [IDA, ISO]
- ribosome 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
mTOR controls mitochondrial oxidative function through a YY1-PGC-1alpha transcriptional complex.
Transcriptional complexes that contain peroxisome-proliferator-activated receptor coactivator (PGC)-1alpha control mitochondrial oxidative function to maintain energy homeostasis in response to nutrient and hormonal signals. An important component in the energy and nutrient pathways is mammalian target of rapamycin (mTOR), a kinase that regulates cell growth, size and survival. However, it is unknown whether and how mTOR controls mitochondrial oxidative activities. Here ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| YY1 MTOR | 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