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Corticotropin-releasing hormone receptor 2

From Wikipedia, the free encyclopedia
CRHR2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCRHR2, CRF-RB, CRF2, CRFR2, HM-CRF, corticotropin releasing hormone receptor 2
External IDsOMIM: 602034; MGI: 894312; HomoloGene: 55612; GeneCards: CRHR2; OMA:CRHR2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001202475
NM_001202481
NM_001202482
NM_001202483
NM_001883

NM_001288618
NM_001288619
NM_001288620
NM_009953

RefSeq (protein)

NP_001189404
NP_001189410
NP_001189411
NP_001189412
NP_001874

NP_001275547
NP_001275548
NP_001275549
NP_034083

Location (UCSC)Chr 7: 30.65 – 30.7 MbChr 6: 55.07 – 55.11 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Corticotropin-releasing hormone receptor 2 (CRHR2) is a protein, also known by the IUPHAR-recommended name CRF2,[5] that is encoded by the CRHR2 gene and occurs on the surfaces of some mammalian cells. CRF2 receptors are type 2 G protein-coupled receptors for corticotropin-releasing hormone (CRH) that are resident in the plasma membranes of hormone-sensitive cells. CRH, a peptide of 41 amino acids synthesized in the hypothalamus, is the principal neuroregulator of the hypothalamic-pituitary-adrenal axis, signaling via guanine nucleotide-binding proteins (G proteins) and downstream effectors such as adenylate cyclase. The CRF2 receptor is a multi-pass membrane protein with a transmembrane domain composed of seven helices arranged in a V-shape. CRF2 receptors are activated by two structurally similar peptides, urocortin II, and urocortin III, as well as CRH.[6]

Properties

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The human CRHR2 gene contains 12 exons. Three major functional isoforms, alpha (411 amino acids), beta (438 amino acids), and gamma (397 amino acids), encoded by transcripts with alternative first exons,[7] differ only in the N-terminal sequence comprising the signal peptide and part of the extracellular domain (amino acids 18-108 of CRHR2 alpha); the unique N-terminal sequence of each isoform (34 amino acids in CRHR2 alpha; 61 amino acids in Hs CRHR2 beta; 20 amino acids in CRHR2 gamma) is followed by a sequence common to all isoforms (377 amino acids)[8] comprising most of the multi-pass transmembrane domain followed by a cytoplasmic domain of 47 amino acids.

CRHR2 beta is expressed in human brain; CRHR2 alpha predominates in peripheral tissues. The N-terminal signal peptides of corticotropin-releasing hormone receptor 1 and CRHR2 beta are cleaved off in the endoplasmic reticulum to yield the mature receptors. In contrast, CRHR2 alpha contains a unique pseudo signal peptide that is not removed from the mature receptor. In adenylate cyclase activation assays, CRH-related peptides are 10 times more potent at stimulating CRHR2 beta than CRHR2 alpha and CRHR2 gamma, suggesting that the N-terminal sequence is involved in the ligand-receptor interaction.[9]

See also

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000106113Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000003476Ensembl, 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. ^ "Entrez Gene: CRHR2 corticotropin releasing hormone receptor 2".
  6. ^ Pal K, Swaminathan K, Xu HE, Pioszak AA (Dec 2010). "Structural basis for hormone recognition by the Human CRFR2{alpha} G protein-coupled receptor". The Journal of Biological Chemistry. 285 (51): 40351–61. doi:10.1074/jbc.m110.186072. PMC 3001015. PMID 20966082.
  7. ^ Catalano RD, Kyriakou T, Chen J, Easton A, Hillhouse EW (Mar 2003). "Regulation of corticotropin-releasing hormone type 2 receptors by multiple promoters and alternative splicing: identification of multiple splice variants". Molecular Endocrinology. 17 (3): 395–410. doi:10.1210/me.2002-0302. PMID 12554761.
  8. ^ "Corticotropin-releasing factor receptor 2, UniProtKB/Swiss-Prot Q13324 (CRFR2_HUMAN)".
  9. ^ Hillhouse EW, Grammatopoulos DK (2001). Control of intracellular signalling by corticotropin-releasing hormone in human myometrium. Frontiers of Hormone Research. Vol. 27. pp. 66–74. doi:10.1159/000061042. ISBN 3-8055-7195-X. PMID 11450436.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.