Mediator of RNA polymerase II transcription subunit 1 also known as DRIP205 or Trap220 is a subunit of the Mediator complex and is a protein that in humans is encoded by the MED1 gene.[5][6][7] MED1 functions as a nuclear receptor coactivator.

MED1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMED1, CRSP1, CRSP200, DRIP205, DRIP230, PBP, PPARBP, PPARGBP, RB18A, TRAP220, TRIP2, mediator complex subunit 1
External IDsOMIM: 604311; MGI: 1100846; HomoloGene: 21002; GeneCards: MED1; OMA:MED1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004774

NM_001080118
NM_013634
NM_134027
NM_001361950
NM_001361951

RefSeq (protein)

NP_004765

NP_001073587
NP_038662
NP_598788
NP_001348879
NP_001348880

Location (UCSC)Chr 17: 39.4 – 39.45 MbChr 11: 98.04 – 98.08 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Med1
Identifiers
SymbolMed1
PfamPF10744
InterProIPR019680
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Function

The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The mediator of RNA polymerase II transcription subunit 1 protein is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes [e.g., thyroid hormone receptor-(TR-) associated proteins that interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors]. It also regulates p53-dependent apoptosis and it is essential for adipogenesis. This protein is known to have the ability to self-oligomerize.[7]

Interactions

MED1 has been shown to interact with:

Protein family

This entry represents subunit Med1 of the Mediator complex. The Med1 forms part of the Med9 submodule of the Srb/Med complex. It is one of three subunits essential for viability of the whole organism via its role in environmentally-directed cell-fate decisions.[21]

References

Further reading