Effects of growth hormone on the salmon pituitary proteome

Journal of Proteomics

Volumn 75, Issue 6, 2012, Pages 1718-1731

  Kurata, Yoichi ^a   Kimura, Yayoi ^a   Yamanaka, Yuko ^a   Ishikawa, Akiyo ^a   Okamoto, Hiroyuki ^b   Masaoka, Tetsuji ^b   Nagoya, Hiroyuki ^b   Araki, Kazuo ^b   Moriyama, Shunsuke ^c   Hirano, Hisashi ^a   Mori, Tsukasa ^d  

^a YOKOHAMA CITY UNIVERSITY   (Japan)

^b FISHERIES RESEARCH AGENCY   (Japan)

^c KITASATO UNIVERSITY   (Japan)

^d NIHON UNIVERSITY   (Japan)

Author keywords

Endocrine; GH; Pituitary; Proteome; Salmon

Indexed keywords

GROWTH HORMONE; GROWTH HORMONE 1; HYPOPHYSIS HORMONE; PROLACTIN; SOMATOLACTIN ALPHA; UNCLASSIFIED DRUG;

ARTICLE; CELL GROWTH; CELL PROLIFERATION; CONTROLLED STUDY; ENDOCRINE SYSTEM; GENE EXPRESSION; METABOLISM; NONHUMAN; NUCLEOTIDE SEQUENCE; ONCORHYNCHUS RHODURUS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEOMICS; TRANSCRIPTOMICS;

ANIMALS; ANIMALS, GENETICALLY MODIFIED; CELL PROLIFERATION; FISH PROTEINS; GENE EXPRESSION PROFILING; GROWTH HORMONE; LIPID METABOLISM; ONCORHYNCHUS; PITUITARY GLAND; PITUITARY HORMONES; PROTEOME;

ANIMALIA; ONCORHYNCHUS RHODURUS;

EID: 84857646221     PISSN: 18743919     EISSN: 18767737     Source Type: Journal    
DOI: 10.1016/j.jprot.2011.12.009     Document Type: Article

References (50)

1. Weltzien F.A., Norberg B., Helvik J.V., Andersen Ø., Swanson P., Andersson E. Identification and localization of eight distinct hormone-producing cell types in the pituitary of male Atlantic halibut (Hippoglossus hippoglossus L.). Comp Biochem Physiol A Mol Integr Physiol 2003, 134:315-327.
2. Ooi G.T., Tawadros N., Escalona R.M. Pituitary cell lines and their endocrine applications. Mol Cell Endocrinol 2004, 228:1-21.
3. Breves J.P., Seale A.P., Helms R.E., Tipsmark C.K., Hirano T., Grau E.G. Dynamic gene expression of GH/PRL-family hormone receptors in gill and kidney during freshwater-acclimation of Mozambique tilapia. Comp Biochem Physiol A Mol Integr Physiol 2011, 158:194-200.
4. Ben-Jonathan N., Hugo E.R., Brandebourg T.D., LaPensee C.R. Focus on prolactin as a metabolic hormone. Trends Endocrinol Metab 2006, 17:110-116.
5. Sundström L.F., Devlin R.H., Johnsson J.I., Biagi C.A. Vertical position reflects increased feeding motivation in growth hormone transgenic coho salmon (Oncorhynchus kisutch). Ethology 2003, 109:701-712.
6. Sambroni E., Abdennebi-Najar L., Remy J.J., Le Gac F. Delayed sexual maturation through gonadotropin receptor vaccination in the rainbow trout Oncorhynchus mykiss. Gen Comp Endocrinol 2009, 164:107-116.
7. Wong A.O., Zhou H., Jiang Y., Ko W.K. Feedback regulation of growth hormone synthesis and secretion in fish and the emerging concept of intrapituitary feedback loop. Comp Biochem Physiol A Mol Integr Physiol 2006, 144:284-305.
8. Agellon L.B., Davies S.L., Lin C.M., Chen T.T., Powers D.A. Rainbow trout has two genes for growth hormone. Mol Reprod Dev 1988, 1:11-17.
9. Mori T., Deguchi F., Ueno K. Differential expression of Gh1 and Gh 2 genes by competitive RT-PCR in rainbow trout pituitary. Gen Comp Endocrinol 2001, 123:137-143.
10. Melmed S. Acromegaly pathogenesis and treatment. J Clin Invest 2009, 119:3189-3202.
11. Perrini S., Laviola L., Carreira M.C., Cignarelli A., Natalicchio A., Giorgino F. The GH/IGF1 axis and signaling pathways in the muscle and bone: mechanisms underlying age-related skeletal muscle wasting and osteoporosis. J Endocrinol 2010, 205:201-210.
12. Rius-Francino M., Acerete L., Jiménez-Amilburu V., Capilla E., Navarro I., Gutiérrez J. Differential effects on proliferation of GH and IGFs in sea bream(Sparus aurata) cultured myocytes. Gen Comp Endocrinol 2011, 172:44-49.
13. Madsen K., Friberg U., Roos P., Edén S., Isaksson O. Growth hormone stimulates the proliferation of cultured chondrocytes from rabbit ear and rat rib growth cartilage. Nature 1983, 304:545-547.
14. Johnsson Jorgen I., Bjornsson Bjorn Th. Growth hormone increases growth rate, appetite and dominance in juvenile rainbow trout, Oncorhynchus mykiss. Anim Behav 1994, 48:177-186.
15. Devlin R.H., Sakhrani D., Tymchuk W.E., Rise M.L., Goh B. Domestication and growth hormone transgenesis cause similar changes in gene expression in coho salmon (Oncorhynchus kisutch). Proc Natl Acad Sci USA 2009, 106:3047-3052.
16. Devlin R.H., Biagi C.A., Yesaki T.Y. Growth, viability and genetic characteristics of GH transgenic coho salmon strains. Aquaculture 2004, 236:607-632.
17. Rahman M.A., Mak R., Ayad H., Smith A., Maclean N. Expression of a novel piscine growth hormone gene results in growth enhancement in transgenic tilapia (Oreochromis niloticus). Transgenic Res 1998, 7:357-369.
18. Sheridan M.A. Effects of thyroxin, cortisol, growth hormone, and prolactin on lipid metabolism of coho salmon, Oncorhynchus kisutch, during smoltification. Gen Comp Endocrinol 1986, 64:220-238.
19. Krasnov A., Agren J.J., Pitäknen T.I., Mölsä H. Transfer of growth hormone (GH)transgenes into Arctic charr. (Salvelinus alpinus L.) II. Nutrient partitioning in rapidly growing fish. Genet Anal 1999, 15:99-105.
20. Falcón J., Besseau L., Fazzari D., Attia J., Gaildrat P., Beauchaud M., et al. Melatonin modulates secretion of growth hormone and prolactin by trout pituitary glands and cells in culture. Endocrinology 2003, 144:4648-4658.
21. Shilov I.V., Seymour S.L., Patel A.A., Loboda A., Tang W.H., Keating S.P., et al. The Paragon Algorithm, a next generation search engine that uses sequence temperature values and feature probabilities to identify peptides from tandem mass spectra. Mol Cell Proteomics 2007, 6:1638-1655.
22. Tang W.H., Shilov I.V., Seymour S.L. Nonlinear fitting method for determining local false discovery rates from decoy database searches. J Proteome Res 2008, 7:3661-3667.
23. Mori T., Hiraka I., Kurata Y., Kawachi H., Mano N., Devlin R.H., et al. Changes in hepatic gene expression related to innate immunity, growth and iron metabolism in GH-transgenic amago salmon (Oncorhynchus masou) by cDNA subtraction and microarray analysis, and serum lysozyme activity. Gen Comp Endocrinol 2007, 151:42-54.
24. Shimizu M., Swanson P., Fukada H., Hara A., Dickhoff W.W. Comparison of extraction methods and assay validation for salmon insulin-like growth factor-I using commercially available components. Gen Comp Endocrinol 2000, 119:26-36.
25. Swanson P. Radioimmunoassay of fish growth hormone, prolactin, and somatolactin. Biochemistry and Molecular Biology of Fishes. 1994, vol 3:545-556. Elsevier Inc, Amsterdam. P.W. Hochachka, T.P. Mommsen (Eds.).
26. Moriyama S., Swanson P., Nishii M., Takahashi A., Kawauchi H., Dickhoff W.W., et al. Development of a homologous radioimmunoassay for coho salmon insulin-like growth factor-I. Gen Comp Endocrinol 1994, 96:149-161.
27. Mori T., Kawachi H., Imai C., Sugiyama M., Kurata Y., Kishida O., et al. Identification of a novel uromodulin-like gene related to predator-induced bulgy morph in anuran tadpoles by functional microarray analysis. PLoS One 2009, 4:e5936.
28. Jiang Q., Ko W.K., Lerner E.A., Chan K.M., Wong A.O. Grass carp somatolactin: I. Evidence for PACAP induction of somatolactin-alpha and -beta gene expression via activation of pituitary PAC-I receptors. Am J Physiol Endocrinol Metab 2008, 295:E463-E476.
29. Manzon L.A. The role of prolactin in fish osmoregulation: a review. Gen Comp Endocrinol 2002, 125:291-310.
30. Chitalia V.C., Foy R.L., Bachschmid M.M., Zeng L., Panchenko M.V., Zhou M.I., et al. Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL. Nat Cell Biol 2008, 10:1208-1216.
31. Waite E., Lafont C., Carmignac D., Chauvet N., Coutry N., Christian H., et al. Different degrees of somatotroph ablation compromise pituitary growth hormone cell network structure and other pituitary endocrine cell types. Endocrinology 2010, 151:234-243.
32. Haisenleder D.J., Burger L.L., Aylor K.W., Dalkin A.C., Marshall J.C. Gonadotropin-releasing hormone stimulation of gonadotropin subunit transcription: evidence for the involvement of calcium/calmodulin-dependent kinase II (Ca/CAMKII) activation in rat pituitaries. Endocrinology 2003, 144:2768-2774.
33. Wong A.O., Li W., Leung C.Y., Huo L., Zhou H. Pituitary adenylate cyclase-activating polypeptide (PACAP) as a growth hormone (GH)-releasing factor in grass carp. I. Functional coupling of cyclic adenosine 3',5'-monophosphate and Ca2+/calmodulin-dependent signaling pathways in PACAP-induced GH secretion and GH gene expression in grass carp pituitary cells. Endocrinology 2005, 146:5407-5424.
34. Zhu X., Zhou A., Dey A., Norrbom C., Carroll R., Zhang C., et al. Disruption of PC1/3 expression in mice causes dwarfism and multiple neuroendocrine peptide processing defects. Proc Natl Acad Sci USA 2002, 99:10293-10298.
35. Jackson R.S., Creemers J.W., Ohagi S., Raffin-Sanson M.L., Sanders L., Montague C.T., et al. Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene. Nat Genet 1997, 16:303-306.
36. López-Ríos F., Sánchez-Aragó M., García-García E., Ortega A.D., Berrendero J.R., Pozo-Rodríguez F., et al. Loss of the mitochondrial bioenergetic capacity underlies the glucose avidity of carcinomas. Cancer Res 2007, 67:9013-9017.
37. Vander Heiden M.G., Cantley L.C., Thompson C.B. Understanding the Warburg effect: the metabolic requirements of cell proliferation. Science 2009, 324:1029-1033.
38. Cai Z., Zhao J.S., Li J.J., Peng D.N., Wang X.Y., Chen T.L., et al. A combined proteomics and metabolomics profiling of gastric cardia cancer reveals characteristic dysregulations in glucose metabolism. Mol Cell Proteomics 2010, 9:2617-2628.
39. Chen A., Kaganovsky E., Rahimipour S., Ben-Aroya N., Okon E., Koch Y. Two forms of gonadotropin-releasing hormone (GnRH) are expressed in human breast tissue and overexpressed in breast cancer: a putative mechanism for the antiproliferative effect of GnRH by down-regulation of acidic ribosomal phosphoproteins P1 and P2. Cancer Res 2002, 62:1036-1044.
40. Barna M., Pusic A., Zollo O., Costa M., Kondrashov N., Rego E., et al. Suppression of Myc oncogenic activity by ribosomal protein haploinsufficiency. Nature 2008, 456:971-975.
41. Li M., Chen D., Shiloh A., Luo J., Nikolaev A.Y., Qin J., et al. Deubiquitination of p53 by HAUSP is an important pathway for p53 stabilization. Nature 2002, 416:648-653.
42. Li M., Brooks C.L., Kon N., Gu W. A dynamic role of HAUSP in the p53-Mdm2 pathway. Mol Cell 2004, 13:879-886.
43. Huang Z., Wu Q., Guryanova O.A., Cheng L., Shou W., Rich J.N., et al. Deubiquitylase HAUSP stabilizes REST and promotes maintenance of neural progenitor cells. Nat Cell Biol 2011, 13:142-152.
44. Schulthess F.T., Katz S., Ardestani A., Kawahira H., Georgia S., Bosco D., et al. Deletion of the mitochondrial flavoprotein apoptosis inducing factor(AIF) induces beta-cell apoptosis and impairs beta-cell mass. PLoS One 2009, 4:e4394.
45. Artero-Castro A., Callejas F.B., Castellvi J., Kondoh H., Carnero A., Fernández-Marcos P.J., et al. Cold-inducible RNA-binding protein bypasses replicative senescence in primary cells through extracellular signal-regulated kinase 1 and 2 activation. Mol Cell Biol 2009, 29:1855-1868.
46. Zeng Y., Kulkarni P., Inoue T., Getzenberg R.H. Down-regulating cold shock protein genes impairs cancer cell survival and enhances chemosensitivity. J Cell Biochem 2009, 107:179-188.
47. Alvarez C.V., Zalvide J.B., Cancio E., Dieguez C., Regueiro B.J., Vega F.V., et al. Regulation of prothymosin alpha mRNA levels in rat pituitary tumor cells. Neuroendocrinology 1993, 57:1048-1056.
48. DeBerardinis R.J., Lum J.J., Hatzivassiliou G., Thompson C.B. The biology of cancer: metabolic reprogramming fuels cell growth and proliferation. Cell Metab 2008, 7:11-20.
49. Menendez J.A., Lupu R. Fatty acid synthase and the lipogenic phenotype in cancer pathogenesis. Nat Rev Cancer 2007, 7:763-777.
50. Mori T., Devlin R.H. Transgene and host growth hormone gene expression in pituitary and nonpituitary tissues of normal and growth hormone transgenic salmon. Mol Cell Endocrinol 1999, 149:129-139.