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Melanocortin 3 receptor

From Wikipedia, the free encyclopedia
Mammalian protein found in Homo sapiens
MC3R
Identifiers
AliasesMC3R, BMIQ9, MC3, MC3-R, OB20, OQTL, Melanocortin 3 receptor
External IDsOMIM:155540;MGI:96929;HomoloGene:7412;GeneCards:MC3R;OMA:MC3R - orthologs
Gene location (Human)
Chromosome 20 (human)
Chr.Chromosome 20 (human)[1]
Chromosome 20 (human)
Genomic location for MC3R
Genomic location for MC3R
Band20q13.2Start56,248,732bp[1]
End56,249,815bp[1]
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)[2]
Chromosome 2 (mouse)
Genomic location for MC3R
Genomic location for MC3R
Band2 H3|2 94.8 cMStart172,090,412bp[2]
End172,093,034bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • deltoid muscle

  • Hypothalamus

  • prefrontal cortex

  • sensory organ

  • mucosa of nose

  • superior frontal gyrus

  • olfactory zone of nasal mucosa

  • dorsolateral prefrontal cortex

  • wall of uterus

  • endometrium
Top expressed in
  • embryo

  • gastrula

  • lumbar subsegment of spinal cord

  • meninges

  • arcuate nucleus

  • skin of abdomen

  • nucleus of stria terminalis

  • region of wall of ventricular system of neuraxis

  • ventricular system

  • choroid plexus
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

4159

17201

Ensembl

ENSG00000124089

ENSMUSG00000038537

UniProt

P41968

P33033

RefSeq (mRNA)

NM_019888

NM_008561

RefSeq (protein)

NP_063941

NP_032587

Location (UCSC)Chr 20: 56.25 – 56.25 MbChr 2: 172.09 – 172.09 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Melanocortin 3 receptor (MC3R) is aprotein that in humans is encoded by theMC3Rgene.[5][6]

Function

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This gene encodes MC3R, aG-protein coupled receptor (GPCR) formelanocyte-stimulating hormone (MSH) andadrenocorticotropic hormone (ACTH) that is expressed in the brain. This gene maps to the same region as thelocus for benign neonatal epilepsy. Mice deficient for this gene have increased fat mass, reduced lean mass and decreased food intake, all suggesting a role for the receptor in the regulation of energy homeostasis.[6]MC3R mutations has been linked to reduced growth rate during childhood and a delay in the age ofpuberty onset.[7]

Research

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Studies performed by the Eunice Kennedy Shriver National Institute of Child Health and Human Development(NICHD), found that two specific polymorphisms in theMC3R gene may be associated with pediatric obesity and greater body mass because of greater energy intake. Children who were homozygous for C17A + G241A consumed approximately 38% more than those who did not contain aforementioned polymorphisms. The study concluded that these genetic variants did not affect energy expenditure.[8]

Ligands

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Evolution

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Paralogue

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Source:[13]

See also

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References

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  1. ^abcGRCh38: Ensembl release 89: ENSG00000124089Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000038537Ensembl, 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. ^Gantz I, Konda Y, Tashiro T, Shimoto Y, Miwa H, Munzert G, Watson SJ, DelValle J, Yamada T (April 1993)."Molecular cloning of a novel melanocortin receptor".The Journal of Biological Chemistry.268 (11):8246–50.doi:10.1016/S0021-9258(18)53088-X.PMID 8463333.
  6. ^ab"Entrez Gene: MC3R melanocortin 3 receptor".
  7. ^Lam, B.Y.H., Williamson, A., Finer, S. et al. MC3R links nutritional state to childhood growth and the timing of puberty. Nature (2021).doi:10.1038/s41586-021-04088-9
  8. ^Savastano DM, Tanofsky-Kraff M, Han JC, Ning C, Sorg RA, Roza CA, Wolkoff LE, Anandalingam K, Jefferson-George KS, Figueroa RE, Sanford EL, Brady S, Kozlosky M, Schoeller DA, Yanovski JA (October 2009)."Energy intake and energy expenditure among children with polymorphisms of the melanocortin-3 receptor".The American Journal of Clinical Nutrition.90 (4):912–20.doi:10.3945/ajcn.2009.27537.PMC 2744620.PMID 19656839.
  9. ^Fleming KA, Freeman KT, Powers MD, Santos RG, Debevec G, Giulianotti MA, et al. (March 2019)."Discovery of Polypharmacological Melanocortin-3 and -4 Receptor Probes and Identification of a 100-Fold Selective nM MC3R Agonist versus a μM MC4R Partial Agonist".Journal of Medicinal Chemistry.62 (5):2738–2749.doi:10.1021/acs.jmedchem.9b00053.PMC 6463894.PMID 30741545.
  10. ^Ericson MD, Shaikh R, Larson CM, Freeman KT, Haskell-Luevano C (January 2021)."Multiresidue Tetrapeptide Substitutions Yield a 140-fold Selective Melanocortin-3 over Melanocortin-4 Receptor Agonist".ACS Medicinal Chemistry Letters.12 (1):115–120.doi:10.1021/acsmedchemlett.0c00561.PMC 7812669.PMID 33488972.
  11. ^Doering SR, Freeman K, Debevec G, Geer P, Santos RG, Lavoi TM, et al. (May 2021)."Discovery of Nanomolar Melanocortin-3 Receptor (MC3R)-Selective Small Molecule Pyrrolidine Bis-Cyclic Guanidine Agonist Compounds Via a High-Throughput "Unbiased" Screening Campaign".Journal of Medicinal Chemistry.64 (9):5577–5592.doi:10.1021/acs.jmedchem.0c02041.PMC 8552302.PMID 33886285.
  12. ^Cai M, Mayorov AV, Ying J, Stankova M, Trivedi D, Cabello C, Hruby VJ (August 2005). "Design of novel melanotropin agonists and antagonists with high potency and selectivity for human melanocortin receptors".Peptides.26 (8):1481–1485.doi:10.1016/j.peptides.2005.03.020.PMID 15876475.S2CID 45499654.
  13. ^"GeneCards®: The Human Gene Database".

Further reading

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External links

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This article incorporates text from theUnited States National Library of Medicine, which is in thepublic domain.

Neurotransmitter
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