CCK(-like) and receptors: Structure and phylogeny in a comparative perspective

General and Comparative Endocrinology

Volumn 209, Issue , 2014, Pages 74-81

  Yu, Na ^a   Smagghe, Guy ^a  

^a GHENT UNIVERSITY   (Belgium)

Author keywords

Cholecystokinin; NLP 12; Phylogeny; Receptor; Structure; Sulfakinin

Indexed keywords

CHOLECYSTOKININ; CHOLECYSTOKININ DERIVATIVE; CHOLECYSTOKININ RECEPTOR; CHOLECYSTOKININ RECEPTOR 1; CHOLECYSTOKININ RECEPTOR 2; CIONIN; CIONIN RECEPTOR; GASTRIN; NEUROPEPTIDE; NEUROPEPTIDE LIKE PROTEIN 12; SULFAKININ; SULFAKININ RECEPTOR; UNCLASSIFIED DRUG; PROTEIN BINDING;

AMINO ACID SEQUENCE; ANXIETY; ARTHROPOD; ARTICLE; COMPARATIVE STUDY; ENZYME RELEASE; FEEDING BEHAVIOR; GASTROINTESTINAL MOTILITY; GENE DELETION; GENE DUPLICATION; LAST COMMON ANCESTOR; MEMORY; MOLECULAR EVOLUTION; MOLECULAR PHYLOGENY; NEMATODE; NONHUMAN; NUCLEOTIDE SEQUENCE; PANCREAS SECRETION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; SATIETY; SEQUENCE ALIGNMENT; SIGNAL TRANSDUCTION; STOMACH ACID SECRETION; UROCHORDATA; ANIMAL; CHEMISTRY; CLASSIFICATION; EVOLUTION; GENETICS; HUMAN; INVERTEBRATE; MOLECULAR GENETICS; PHYLOGENY; PROTEIN CONFORMATION; VERTEBRATE;

AMINO ACID SEQUENCE; ANIMALS; BIOLOGICAL EVOLUTION; CHOLECYSTOKININ; HUMANS; INVERTEBRATES; MOLECULAR SEQUENCE DATA; PHYLOGENY; PROTEIN BINDING; PROTEIN CONFORMATION; RECEPTORS, CHOLECYSTOKININ; VERTEBRATES;

EID: 84914142539     PISSN: 00166480     EISSN: 10956840     Source Type: Journal    
DOI: 10.1016/j.ygcen.2014.05.003     Document Type: Article

References (75)

1. Bi S., Moran T.H. Actions of CCK in the controls of food intake and body weight: lessons from the CCK-A receptor deficient OLETF rat. Neuropeptides 2002, 36:171-181.
2. Cao Z., Yu Y., Wu Y., Hao P., Di Z., He Y., et al. The genome of Mesobuthus martensii reveals a unique adaptation model of arthropods. Nat. Commun. 2013, 4:2602.
3. Cardoso J.C., Félix R.C., Fonseca V.G., Power D.M. Feeding and the rhodopsin family G-protein coupled receptors in nematodes and arthropods. Front. Endocrinol. (Lausanne) 2012, 3:157.
4. Christie A.E. In silico analyses of peptide paracrines/hormones in Aphidoidea. Gen. Comp. Endocrinol. 2008, 159:67-79.
5. Christie A.E. Neuropeptide discovery in Ixodoidea: an in silico investigation using publicly accessible expressed sequence tags. Gen. Comp. Endocrionol. 2008, 157:174-185.
6. Christie A.E., Cashman C.R., Brennan H.R., Ma M., Sousa G.L., Li L., et al. Identification of putative crustacean neuropeptides using in silico analysis of publicly accessible expressed sequence tags. Gen. Comp. Endocrinol. 2008, 156:246-264.
7. Christie A.E., McCoole M.D., Harmon S.M., Baer K.N., Lenz P.H. Genomic analysis of the Daphnia pulex peptidome. Gen. Comp. Endocrinol. 2011, 171:131-150.
8. Christie A.E., Nolan D.H., Ohno P., Hartline N., Lenz P.H. Identification of chelicerate neuropeptides using bioinformatics of publicly accessible expressed sequence tags. Gen. Comp. Endocrinol. 2011, 170:144-155.
9. Chen X., Peterson J., Nachman R.J., Ganetzky B. Drosulfakinin activates CCKLR-17D1 and promotes larval locomotion and escape response in Drosophila. Fly 2012, 6:290-297.
10. Coast G.M., Schooley D.A. Toward a consensus nomenclature for insect neuropeptides and peptide hormones. Peptides 2011, 32:620-631.
11. De Tullio P., Delarge J., Pirotte B. Therapeutic and chemical developments of cholecystokinin receptor ligands. Expert Opin. Investig. Drugs 2000, 9:129-146.
12. Deweerth A., Pisegna J.R., Huppi K., Wank S.A. Molecular cloning, functional expression and chromosomal localization of the human cholecystokinin type A receptor. Biochem. Biophys. Res. Commun. 1993, 194:811-818.
13. Dickinson P.S., Stevens J.S., Rus S., Brennan H.R., Goiney C.C., Smith C.M., et al. Identification and cardiotropic actions of sulfakinin peptides in the American lobster Homarus americanus. J. Exp. Biol. 2007, 210:2278-2289.
14. Dimaline R., Dockray G.J. Evolution of the gastrointestinal endocrine system (with special reference to gastrin and CCK). Baillière's Clin. Endocrinol. Metab. 1994, 8:1-24.
15. Dockray G. Molecular evolution of gut hormones: application of comparative studies on the regulation of digestion. Gastroenterology 1977, 72:344-358.
16. Dockray G., Varro A., Dimaline R., Wang T. The gastrins: their production and biological activities. Annu. Rev. Physiol. 2001, 63:119-139.
17. Downer K.E., Haselton A.T., Nachman R.J., Stoffolano J.G. Insect satiety: sulfakinin localization and the effect of drosulfakinin on protein and carbohydrate ingestion in the blow fly, Phormia regina (Diptera: Calliphoridae). J. Insect Physiol. 2007, 53:106-112.
18. Dufresne M., Seva C., Fourmy D. Cholecystokinin and gastrin receptors. Physiol. Rev. 2006, 86:805-847.
19. Dupré D., Tostivint H. Evolution of the gastrin-cholecystokinin gene family revealed by synteny analysis. Gen. Comp. Endocrinol. 2014, 195:164-173.
20. Eysselein V.E., Eberlein G.A., Schaeffer M., Grandt D., Goebell H., Niebel W., et al. Characterization of the major form of cholecystokinin in human intestine: CCK-58. Am. J. Physiol. 1990, 258:G253-G260.
21. Fan Y., Sun P., Wang Y., He X., Deng X., Chen X., et al. The G protein-coupled receptors in the silkworm. Bombyx mori. Insect Biochem. Mol. Biol. 2010, 40:581-591.
22. Harshini S., Nachman R., Sreekumar S. In vitro release of digestive enzymes by FMRFamide related neuropeptides and analogues in the lepidopteran insect Opisina arenosella (Walk.). Peptides 2002, 23:1759-1763.
23. Hauser F., Cazzamali G., Williamson M., Blenau W., Grimmelikhuijzen C.J. A review of neurohormone GPCRs present in the fruitfly Drosophila melanogaster and the honey bee Apis mellifera. Prog. Neurobiol. 2006, 80:1-19.
24. Hauser F., Cazzamali G., Williamson M., Park Y., Li B., Tanaka Y., Predel R., Neupert S., Schachtner J., Verleyen P., Grimmelikhuijzen C.J. A genome-wide inventory of neurohormone GPCRs in the red flour beetle Tribolium castaneum. Front. Neuroendocrinol. 2008, 29:142-165.
25. Hauser F., Neupert S., Williamson M., Predel R., et al. Genomics and peptidomics of neuropeptides and protein hormones present in the parasitic wasp Nasonia vitripennis. J. Proteome Res. 2010, 9:5296-5310.
26. Hauser F., Williamson M., Cazzamali G., Grimmelikhuijzen C.J. Identifying neuropeptide and protein hormone receptors in Drosophila melanogaster by exploiting genomic data. Brief Funct. Genomic Proteomic 2006, 4:321-330.
27. Hoffmann W., Bach T., Seliger H., Kreil G. Biosynthesis of caerulein in the skin of Xenopus laevis: partial sequences of precursors as deduced from cDNA clones. EMBO J. 1983, 2:111-114.
28. Huppi K., Siwarski D., Pisegna J., Wank S. Chromosomal localization of the gastric and brain receptors for cholecystokinin (CCKAR and CCKBR) in human and mouse. Genomics 1995, 25:727-729.
29. Janssen T., Meelkop E., Lindemans M., Verstraelen K., Husson S.J., Temmerman L., Nachman R.J., Schoofs L. Discovery of a cholecystokinin-gastrin-like signalling system in nematodes. Endocrinology 2008, 149:2826-2839.
30. Jensen R.T. Involvement of Cholecystokinin/gastrin-related peptides and their receptors in clinical gastrointestinal disorders. Pharmacol. Toxicol. 2002, 91:333-350.
31. Johnsen A.H. Phylogeny of the cholecystokinin/gastrin family. Front. Neuroendocrinol. 1998, 19:73-99.
32. Johnsen A.H., Duve H., Davey M., Hall M., Thorpe A. Sulfakinin neuropeptides in a crustacean. Isolation, identification and tissue localization in the tiger prawn Penaeus monodon. Eur. J. Biochem. 2000, 267:1153-1160.
33. Johnsen A.H., Rehfeld J. Cionin: a disulfotyrosyl hybrid of cholecystokinin and gastrin from the neural ganglion of the protochordate Ciona intestinalis. J. Biol. Chem. 1990, 265:3054-3058.
34. Kennedy J., Bradwejn J., Koszycki D., King N., Crowe R., Vincent J., et al. Investigation of cholecystokinin system genes in panic disorder. Mol. Psychiatry 1999, 4:284-285.
35. Kubiak T.M., Larsen M.J., Burton K.J., Bannow C.A., Martin R.A., Zantello M.R., et al. Cloning and functional expression of the first Drosophila melanogaster sulfakinin receptor DSK-R1. Biochem. Biophys. Res. Commun. 2002, 291:313-320.
36. Larsson L.I., Rehfeld J. Evidence for a common evolutionary origin of gastrin and cholecystokinin. Nature 1977, 269:335-338.
37. Li C. The ever-expanding neuropeptide gene families in the nematode Caenorhabditis elegans. Parasitology 2005, 131:S109-S127.
38. Li C., Yun X., Hu X., Zhang Y. Identification of G protein-coupled receptors in the pea aphid, Acyrthosiphon pisum. Genomics 2013, 102:345-354.
39. Maestro J.L., Aguilar R., Pascual N., Valero M.L., Piulachs M.D., Andreu D., et al. Screening of antifeedant activity in brain extracts led to the identification of sulfakinin as a satiety promoter in the German cockroach. Eur. J. Biochem. 2001, 268:5824-5830.
40. Mårvik R., Johnsen A., Rehfeld J., Sandvik A., Waldum H. Effect of cionin on histamine and acid secretion by the perfused rat stomach. Scand. J. Gastroenterol. 1994, 29:591-594.
41. McVeigh P., Leech S., Marks N.J., Geary T.G., Maule A.G. Gene expression and pharmacology of nematode NLP-12 neuropeptides. Int. J. Parasitol. 2006, 36:633-640.
42. Meyering-Vos M., Müller A. RNA interference suggests sulfakinins as satiety effectors in the cricket Gryllus bimaculatus. J. Insect Physiology. 2007, 53:840-848.
43. Meyering-Vos M., Müller A. Structure of the sulfakinin cDNA and gene expression from the Mediterranean field cricket Gryllus bimaculatus. Insect Mol. Biol. 2007, 16:445-454.
44. Mirabeau O., Joly J.S. Molecular evolution of peptidergic signaling systems in bilaterians. Proc Natl Acad Sci USA 2013, 110:E2028-E2037.
45. Nachman R.J., Giard W., Favrel P., Suresh T., Sreekumar S., Holman G. Insect myosuppressins and sulfakinins stimulate release of the digestive enzyme α-amylase in two invertebrates: the scallop Pecten maximus and insect Rhynchophorus ferrugineus. Ann. N. Y. Acad. Sci. 1997, 814:335-338.
46. Nachman R.J., Holman G.M., Cook B.J., Haddon W.F., Ling N. Leucosulfakinin-II, a blocked sulfated insect neuropeptide with homology to cholecystokinin and gastrin. Biochem. Biophys. Res. Commun. 1986, 140:357-364.
47. Nachman R.J., Holman G.M., Haddon W.F., Ling N. Leucosulfakinin, a sulfated insect neuropeptide with homology to gastrin and cholecystokinin. Science 1986, 234:71-73.
48. Nichols R. The first nonsulfated sulfakinin activity reported suggests nsDSK acts in gut biology. Peptides 2007, 28:767-773.
49. Nichols R., Manoogian B., Walling E., Mispelon M. Plasticity in the effects of sulfated and nonsulfated sulfakinin on heart contractions. Front Biosci. (Landmark Ed.) 2009, 14:4035-4043.
50. Nichols R., Schneuwly S., Dixon J. Identification and characterization of a Drosophila homologue to the vertebrate neuropeptide cholecystokinin. J. Biol. Chem. 1988, 263:12167-12170.
51. Nilsson I., Svensson S.P., Monstein H.J. Molecular cloning of a putative Ciona intestinalis cionin receptor, a new member of the CCK/gastrin receptor family. Gene 2003, 323:79-88.
52. Noble F., Roques B.P. CCK-B receptor: chemistry, molecular biology, biochemistry and pharmacology. Prog. Neurobiol. 1999, 58:349-379.
53. Nygaard S., Zhang G., Schiøtt M., Li C., Wurm Y., Hu H., Zhou J., et al. The genome of the leaf-cutting ant Acromyrmex echinatior suggests key adaptations to advanced social life and fungus farming. Genome Res. 2011, 21:1339-1348.
54. Omasits U., Ahrens C.H., Müller S., Wollscheid B. Protter: interactive protein feature visualization and integration with experimental proteomic data. Bioinformatics 2014, 30:884-886.
55. Predel R., Rapus J., Eckert M. Myoinhibitory neuropeptides in the American cockroach. Peptides 2001, 22:199-208.
56. Rehfeld J.F., Friis-Hansen L., Goetze J.P., Hansen T.V. The biology of cholecystokinin and gastrin peptides. Curr. Top. Med. Chem. 2007, 7:1154-1165.
57. Savard J., Tautz D., Lercher M.J. Genome-wide acceleration of protein evolution in flies (Diptera). BMC Evol. Biol. 2006, 6:7.
58. Schjoldager B., Jørgensen J.C., Johnsen A.H. Stimulation of rainbow trout gallbladder contraction by cionin, an ancestral member of the CCK/gastrin family. Gen. Comp. Endocrinol. 1995, 98:269-278.
59. Schmitz F., Pratt D.S., Wu M.J., Kolakowski L., Beinborn M., Kopin A.S. Identification of cholecystokinin-B/gastrin receptor domains that confer high gastrin affinity: utilization of a novel Xenopus laevis cholecystokinin receptor. Mol. Pharmacol. 1996, 50:436-441.
60. Sekiguchi T., Ogasawara M., Satake H. Molecular and functional characterization of cionin receptors in the ascidian, Ciona intestinalis: the evolutionary origin of the vertebrate cholecystokinin/gastrin family. J. Endocrinol. 2012, 213:99-106.
61. Singh M., Webster P.D. Neurohormonal control of pancreatic secretion: a review. Gastroenterology 1978, 74:294-309.
62. Staljanssens D., Azari E.K., Christiaens O., Beaufays J., Lins L., Van Camp J., et al. The CCK(-like) receptor in the animal kingdom: functions, evolution and structures. Peptides 2011, 32:607-619.
63. Taghert P.H., Nitabach M.N. Peptide neuromodulation in invertebrate model systems. Neuron. 2012, 76:82-97.
64. Tamura K., Peterson D., Peterson N., Stecher G., Nei M., Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol. Biol. Evol. 2011, 28:2731-2739.
65. Tanaka Y., Suetsugu Y., Yamamoto K., Noda H., Shinoda T. Transcriptome analysis of neuropeptides and G-protein coupled receptors (GPCRs) for neuropeptides in the brown planthopper Nilaparvata lugens. Peptides 2013, 53:125-133.
66. The International Aphid Genomics Consortium Genome sequence of the pea aphid Acyrthosiphon pisum. PLoS Biol. 2010, 8:e1000313.
67. Thorndyke M., Dockray G. Identification and localization of material with gastrin-like immunoreactivity in the neural ganglion of a protochordate, Ciona intestinalis. Regul. Pept. 1986, 16:269-279.
68. Torfs P., Baggerman G., Meeusen T., Nieto J., Nachman R., Calderon J., et al. Isolation, identification, and synthesis of a disulfated sulfakinin from the central nervous system of an arthropods the white shrimp Litopenaeus vannamei. Biochem. Biophys. Res. Commun. 2002, 299:312-320.
69. Vigna S.R. Evolution of hormone and receptor diversity: cholecystokinin and gastrin. Am. Zool. 1986, 26:1033-1040.
70. Vogel K.J., Brown M.R., Strand M.R. Phylogenetic investigation of peptide hormone and growth factor receptors in five dipteran genomes. Front Endocrinol. (Lausanne) 2013, 4:193.
71. Wei Z., Baggerman G., Nachman R.J., Goldsworthy G., Verhaert P., De Loof A., et al. Sulfakinins reduce food intake in the desert locust, Schistocerca gregaria. J. Insect Physiol. 2000, 46:1259-1265.
72. 2+-mobilizing hormones in Xenopus oocytes. Proc. Natl. Acad. Sci. USA 1988, 85:4939-4943.
73. Wyder S., Kriventseva E.V., Schröder R., Kadowaki T., Zdobnov E.M. Quantification of ortholog losses in insects and vertebrates. Genome Biol. 2007, 8:R242.
74. Yu N., Nachman R.J., Smagghe G. Characterization of sulfakinin and sulfakinin receptor and their roles in food intake in the red flour beetle Tribolium castaneum. Gen. Comp. Endocrinol. 2013, 188:196-203.
75. Yu N., Smagghe G. Characterization of sulfakinin receptor 2 and its role in food intake in the red flour beetle, Tribolium castaneum. Peptides 2014, 53:232-237.