Agouti-related peptide

agouti related protein homolog (mouse)
Identifiers
Symbols AGRP; AGRT; ASIP2; MGC118963; ART
External IDs OMIM: 602311 MGI: 892013 HomoloGene: 7184 GeneCards: AGRP Gene
Orthologs
Species Human Mouse
Entrez 181 11604
Ensembl ENSG00000159723 ENSMUSG00000005705
UniProt O00253 P56473
RefSeq (mRNA) NM_007316 NM_007427
RefSeq (protein) NP_001129 NP_031453
Location (UCSC) Chr 16:
66.07 – 66.08 Mb		 Chr 8:
108.09 – 108.09 Mb
PubMed search [1] [2]
Agouti protein
Identifiers
Symbol Agouti
Pfam PF05039
Pfam clan CL0083
InterPro IPR007733
PROSITE PDOC60024
SCOP 1hyk
OPM protein 1mr0

Agouti-related protein also called Agouti-related peptide (AgRP) is a neuropeptide produced in the brain by the AgRP/NPY neuron. It is only synthesised in NPY containing cell bodies located in the ventromedial part of the arcuate nucleus in the hypothalamus.[1] AgRP is co-expressed with Neuropeptide Y and works by increasing appetite and decreasing metabolism and energy expenditure. It is one of the most potent and long-lasting of appetite stimulators. In humans, the agouti-related peptide is encoded by the AGRP gene.[2][3]

Contents

Structure

AgRP is a paracrine signalling molecule made up of 132 amino acids. It was independently identified by two teams in 1997 based on its sequence similarity with Agouti signalling peptide (ASIP), a protein synthesised in the skin that controls coat colour.[2][3] AgRP is approximately 25% identical to ASIP. The murine homologue of AgRP is made up of 131 amino acids and shares 81% amino acid identity with the human protein. Biochemical studies indicate AgRP is very stable to thermal denaturation and acid degradation. Its secondary structure consists mainly of random coils and β-sheets.[4] AgRP is mapped to human chromosome 16q22 and mouse chromosome 8D1-D2.

Function

Agouti-related protein is primarily expressed in the adrenal gland, subthalamic nucleus and hypothalamus; with lower levels of expression in the testis, kidneys and lungs. The appetite stimulating effects of AgRP are inhibited by the hormone leptin and activated by the hormone ghrelin. Adipocytes secrete leptin in response to food intake. This hormone acts in the arcuate nucleus and inhibits the AgRP/NPY neuron from releasing orexigenic peptides.[5] Ghrelin has receptors on NPY/AgRP neurons that stimulate the secretion of NPY and AgRP to increase appetite. AgRP is stored in intracellular secretory granules and is secreted via a regulated pathway.[6] The transcriptional and secretory action of AgRP is regulated by inflammatory signals.[7] Levels of AgRP are increased during periods of fasting. It has been found that AgRP stimulates the hypothalamic-pituitary-adrenocortical axis to release ACTH, cortisol and prolactin. It also enhances the ACTH response to IL-1-beta, suggesting it may play a role in the modulation of neuroendocrine response to inflammation.[8]

Mechanism

AGRP has been demonstrated to be an inverse agonist of melanocortin receptors, specifically, MC3-R and MC4-R. The melanocortin receptors, MC3-R and MC4-R, are directly linked to metabolism and body weight control. These receptors are activated by the peptide hormone α-MSH (melanocyte-stimulating hormone) and antagonized by the agouti-related protein.[9] Whereas α-MSH acts broadly on most members of the MCR family (with the exception of MC2-R), AGRP is highly specific for only MC3-R and MC4-R. This inverse agonism not only antagonizes the action of melanocortin agonists, such as α-MSH but also further decreases the cAMP produced by the affected cells. The exact mechanism by which AgRP inhibits melanocortin-receptor signalling is not completely clear. It has been suggested that Agouti-related protein binds MSH receptors and acts as a competitive antagonist of ligand binding.[10] Studies of Agouti protein in B16 melanoma cells supported this logic. The expression of AgRP in the adrenal gland is regulated by glucocorticoids. The protein blocks α-MSH induced secretion of corticosterone.[11]

History

Orthologs of AgRP, ASIP, MCIR and MC4R have been found in mammalian, teleost fish and avian genomes. This suggests that the agouti-melanocortin system evolved by gene duplication from individual ligand and receptor genes in the last 500 million years.[9]

Role in Obesity

AgRP induces obesity by chronic antagonism of the MC4-R.[12] Overexpression of AgRP in transgenic mice (or intracerebroventricular injection) causes hyperphagia and obesity,[13] whilst AgRP plasma levels have been found to be elevated in obese human males.[14] Understanding the role AgRP plays in weight gain may assist in developing pharmaceutical models for treating obesity. AgRP mRNA levels have been found to be down regulated following an acute stressful event. Studies suggest that systems involved in the regulation of stress response and of energy balance are highly integrated. Loss or gain of AgRP function may result in inadequate adaptive behavioural responses to environmental events, such as stress, and may potentially contribute to the development of eating disorders. It has been shown that polymorphisms in the AgRP gene have been linked with anorexia nervosa[15] as well as obesity. Some studies suggest that inadequate signalling of AgRP during stress may result in binge eating.

Human proteins containing this domain

AGRP; ASIP

See also

References

  1. ^ Bäckberg M, Madjid N, Ogren SO, Meister B (June 2004). "Down-regulated expression of agouti-related protein (AGRP) mRNA in the hypothalamic arcuate nucleus of hyperphagic and obese tub/tub mice". Brain Res. Mol. Brain Res. 125 (1-2): 129–39. doi:10.1016/j.molbrainres.2004.03.012. PMID 15193430. 
  2. ^ a b Shutter JR, Graham M, Kinsey AC, Scully S, Lüthy R, Stark KL (March 1997). "Hypothalamic expression of ART, a novel gene related to agouti, is up-regulated in obese and diabetic mutant mice". Genes Dev. 11 (5): 593–602. doi:10.1101/gad.11.5.593. PMID 9119224. 
  3. ^ a b Ollmann MM, Wilson BD, Yang YK, Kerns JA, Chen Y, Gantz I, Barsh GS (October 1997). "Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein". Science 278 (5335): 135–8. doi:10.1126/science.278.5335.135. PMID 9311920. 
  4. ^ Rosenfeld RD, Zeni L, Welcher AA, Narhi LO, Hale C, Marasco J, Delaney J, Gleason T, Philo JS, Katta V, Hui J, Baumgartner J, Graham M, Stark KL, Karbon W (November 1998). "Biochemical, biophysical, and pharmacological characterization of bacterially expressed human agouti-related protein". Biochemistry 37 (46): 16041–52. doi:10.1021/bi981027m. PMID 9819197. 
  5. ^ Enriori PJ, Evans AE, Sinnayah P, Jobst EE, Tonelli-Lemos L, Billes SK, Glavas MM, Grayson BE, Perello M, Nillni EA, Grove KL, Cowley MA (March 2007). "Diet-induced obesity causes severe but reversible leptin resistance in arcuate melanocortin neurons". Cell Metabolism 5 (3): 181–94. doi:10.1016/j.cmet.2007.02.004. PMID 17339026. 
  6. ^ Creemers JW, Pritchard LE, Gyte A, Le Rouzic P, Meulemans S, Wardlaw SL, Zhu X, Steiner DF, Davies N, Armstrong D, Lawrence CB, Luckman SM, Schmitz CA, Davies RA, Brennand JC, White A (April 2006). "Agouti-related protein is posttranslationally cleaved by proprotein convertase 1 to generate agouti-related protein (AGRP)83-132: interaction between AGRP83-132 and melanocortin receptors cannot be influenced by syndecan-3". Endocrinology 147 (4): 1621–31. doi:10.1210/en.2005-1373. PMID 16384863. 
  7. ^ Scarlett JM, Zhu X, Enriori PJ, Bowe DD, Batra AK, Levasseur PR, Grant WF, Meguid MM, Cowley MA, Marks DL. (October 2008). "Regulation of agouti-related protein messenger ribonucleic acid transcription and peptide secretion by acute and chronic inflammation". Endocrinology 149 (10): 4837–45. doi:10.1210/en.2007-1680. PMC 2582916. PMID 18583425. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2582916. 
  8. ^ Xiao E, Xia-Zhang L, Vulliémoz NR, Ferin M, Wardlaw SL (May 2003). "Agouti-related protein stimulates the hypothalamic-pituitary-adrenal (HPA) axis and enhances the HPA response to interleukin-1 in the primate". Endocrinology 144 (5): 1736–41. doi:10.1210/en.2002-220013. PMID 12697678. 
  9. ^ a b Jackson PJ, Douglas NR, Chai B, Binkley J, Sidow A, Barsh GS, Millhauser GL (December 2006). "Structural and molecular evolutionary analysis of Agouti and Agouti-related proteins". Chem. Biol. 13 (12): 1297–305. doi:10.1016/j.chembiol.2006.10.006. PMC 2907901. PMID 17185225. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2907901. 
  10. ^ Ollmann MM, Lamoreux ML, Wilson BD, Barsh GS (February 1998). "Interaction of Agouti protein with the melanocortin 1 receptor in vitro and in vivo". Genes Dev. 12 (3): 316–30. doi:10.1101/gad.12.3.316. PMC 316484. PMID 9450927. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=316484. 
  11. ^ Dhillo WS, Small CJ, Gardiner JV, Bewick GA, Whitworth EJ, Jethwa PH, Seal LJ, Ghatei MA, Hinson JP, Bloom SR (January 2003). "Agouti-related protein has an inhibitory paracrine role in the rat adrenal gland". Biochem. Biophys. Res. Commun. 301 (1): 102–7. doi:10.1016/S0006-291X(02)02991-1. PMID 12535647. 
  12. ^ Huszar D, Lynch CA, Fairchild-Huntress V, Dunmore JH, Fang Q, Berkemeier LR, Gu W, Kesterson RA, Boston BA, Cone RD, Smith FJ, Campfield LA, Burn P, Lee F (January 1997). "Targeted disruption of the melanocortin-4 receptor results in obesity in mice". Cell 88 (1): 131–41. doi:10.1016/S0092-8674(00)81865-6. PMID 9019399. 
  13. ^ Graham M, Shutter JR, Sarmiento U, Sarosi I, Stark KL (November 1997). "Overexpression of Agrt leads to obesity in transgenic mice". Nat. Genet. 17 (3): 273–4. doi:10.1038/ng1197-273. PMID 9354787. 
  14. ^ Katsuki A, Sumida Y, Gabazza EC, Murashima S, Tanaka T, Furuta M, Araki-Sasaki R, Hori Y, Nakatani K, Yano Y, Adachi Y (May 2001). "Plasma levels of agouti-related protein are increased in obese men". J. Clin. Endocrinol. Metab. 86 (5): 1921–4. doi:10.1210/jc.86.5.1921. PMID 11344185. 
  15. ^ Vink T, Hinney A, van Elburg AA, van Goozen SH, Sandkuijl LA, Sinke RJ, Herpertz-Dahlmann BM, Hebebrand J, Remschmidt H, van Engeland H, Adan RA (May 2001). "Association between an agouti-related protein gene polymorphism and anorexia nervosa". Mol. Psychiatry 6 (3): 325–8. doi:10.1038/sj.mp.4000854. PMID 11326303. 

Further reading

External links

Intercellular signaling peptides and proteins / ligands
Growth factors
Ephrin
EFNA1 • EFNA2 • EFNA3 • EFNA4 • EFNA5 • EFNB1 • EFNB2 • EFNB3
Other
see also extracellular ligand disorders
B trdu: iter (nrpl/grfl/cytl/horl), csrc (lgic, enzr, gprc, igsr, intg, nrpr/grfr/cytr), itra (adap, gbpr, mapk), calc, lipd; path (hedp, wntp, tgfp+mapp, notp, jakp, fsap, hipp, tlrp)