OGFr

Source: Wikipedia, the free encyclopedia.
OGFR
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_007346

NM_031373

RefSeq (protein)

NP_031372

NP_113550

Location (UCSC)Chr 20: 62.8 – 62.81 MbChr 2: 180.23 – 180.24 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Opioid growth factor receptor (OGFr) conserved region
Identifiers
SymbolOGFr_N
PfamPF04664
InterProIPR006757
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
Opioid growth factor receptor repeat
Identifiers
SymbolOGFr_III
PfamPF04680
InterProIPR006770
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Opioid growth factor receptor, also known as OGFr or the ζ-opioid receptor, is a protein which in humans is encoded by the OGFR gene.[5][6] The protein encoded by this gene is a receptor for opioid growth factor (OGF), also known as [Met(5)]-enkephalin. The endogenous ligand is thus a known opioid peptide, and OGFr was originally discovered and named as a new opioid receptor zeta (ζ). However it was subsequently found that it shares little sequence similarity with the other opioid receptors, and has quite different function.

Function

The natural function of this receptor appears to be in regulation of tissue growth,[7][8][9][10] and it has been shown to be important in embryonic development,[11] wound repair,[12] and certain forms of cancer.[13][14][15][16]

OGF is a negative regulator of cell proliferation and tissue organization in a variety of processes. The encoded unbound receptor for OGF has been localized to the outer nuclear envelope, where it binds OGF and is translocated into the nucleus. The coding sequence of this gene contains a polymorphic region of 60 nt tandem imperfect repeat units. Several transcripts containing between zero and eight repeat units have been reported.[5]

Mechanism of activation

The opioid growth factor receptor consists of a chain of 677 amino acids, which includes a nuclear localization sequence region. When OGF binds to the receptor, an OGF-OGFr complex is formed, which leads to the increase in the synthesis of the selective cyclin-dependent kinase (CDK) inhibitor proteins, p12 and p16. Retinoblastoma protein becomes inactivated through phosphorylation by CDKs, and leads to the progression of the cell cycle from the G1 phase to the S phase. Because the activation of the OGF receptor, blocks the phosphorylation of retinoblastoma proteins, retardation of the G1 phase occurs, which prevents the cell from further dividing.[17][18]

Therapeutic applications

Upregulation of OGFr and consequent stimulation of the OGF-OGFr system are important for the anti-proliferative effects of imidazoquinoline drugs like

antitumour effects, used as topical creams for the treatment of skin cancers and warts.[19]

Structure

OGF contains a

N-terminal domain followed by a series of imperfect repeats.[8]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000060491Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049401Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: OGFR opioid growth factor receptor".
  6. S2CID 37516655
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Further reading

This article incorporates text from the public domain Pfam and InterPro: IPR006770
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