Visfatin gene expression in chickens is sex and tissue dependent

Domestic Animal Endocrinology

Volumn 38, Issue 2, 2010, Pages 63-74

  Ons, E ^a   Gertler, A ^b   Buyse, J ^a   Lebihan Duval, E ^c   Bordas, A ^d   Goddeeris, B ^a   Dridi, S ^a  

^a LABORATORY OF GENE TECHNOLOGY   (Belgium)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^c STATION DE RECHERCHES AVICOLES   (France)

^d CEMAGREF   (France)

Author keywords

Cerulenin; Chickens; Food deprivation; Genotype; Leptin; Visfatin

Indexed keywords

CERULENIN; LEPTIN; MESSENGER RNA; NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE;

ADIPOSE TISSUE; AMINO ACID SEQUENCE; ANIMAL; ANTIBODY SPECIFICITY; ARTICLE; CHEMISTRY; CHICKEN; DRUG EFFECT; ENERGY METABOLISM; ENZYMOLOGY; FEMALE; FOOD DEPRIVATION; GENE EXPRESSION; GENE EXPRESSION REGULATION; GENETICS; HUMAN; HYPOTHALAMUS; KIDNEY; LIVER; MALE; MUSCLE; PHYLOGENY; PHYSIOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ALIGNMENT; SEX DIFFERENCE;

ADIPOSE TISSUE; AMINO ACID SEQUENCE; ANIMALS; CERULENIN; CHICKENS; ENERGY METABOLISM; FEMALE; FOOD DEPRIVATION; GENE EXPRESSION; GENE EXPRESSION REGULATION; HUMANS; HYPOTHALAMUS; KIDNEY; LEPTIN; LIVER; MALE; MUSCLES; NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE; ORGAN SPECIFICITY; PHYLOGENY; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; SEQUENCE ALIGNMENT; SEX FACTORS;

AVES; GALLUS GALLUS;

EID: 72749118737     PISSN: 07397240     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.domaniend.2009.08.007     Document Type: Article

References (58)

1. Samal B., Sun Y., Stearns G., Xie C., Suggs S., and McNiece I. Cloning and characterization of the cDNA encoding a novel human pre-B-cell colony-enhancing factor. Mol Cell Biol. 14 (1994) 1431-1437
2. McGlothlin J.R., Gao L., Lavoie T., Simon B.A., Easley R.B., Ma S.F., Rumala B.B., Garcia J.G., and Ye S.Q. Molecular cloning and characterization of canine pre-B-cell colony-enhancing factor. Biochem Genet. 43 (2005) 127-141
3. Kloting N., and Kloting I. Visfatin: gene expression in isolated adipocytes and sequence analysis in obese WOKW rats compared with lean control rats. Biochem Biophys Res Commun. 332 (2005) 1070-1072
4. Chen H., Xia T., Zhou L., Chen X., Gan L., Yao W., Pen Y., and Yang Z. Gene organization, alternate splicing and expression pattern of porcine visfatin gene. Domest Anim Endocrinol. 32 (2006) 235-245
5. Jia S.H., Li Y., Parodo J., Kapus A., Fan L., Rotstein O.D., and Marshall J.C. Pre-B cell colony-enhancing factor inhibits neutrophil apoptosis in experimental inflammation and clinical sepsis. J Clin Invest. 113 (2004) 1318-1327
6. Ye S.Q., Simon B.A., Maloney J.P., Zambelli-Weiner A., Gao L., Grant A., Easley R.B., McVerry B.J., Tuder R.M., Standiford T., Brower R.G., Barnes K.C., and Garcia J.G. Pre-B-cell colony-enhancing factor as a potential novel biomarker in acute lung injury. Am J Respir Crit Care Med. 171 (2005) 361-370
7. Ye S.Q., Zhang L.Q., Adyshev D., Usatyuk P.V., Garcia A.N., Lavoie T.L., Verin A.D., Natarajan V., and Garcia J.G. Pre-B-cell colony-enhancing factor is critically involved in thrombin-induced lung endothelial cell barrier dysregulation. Microvascular Res. 70 (2005) 142-151
8. Ognjanovic S., and Bryant-Greenwood G.D. Pre-B-cell colony-enhancing factor, a novel cytokine of human fetal membranes. Am J Obstet Gynecol. 187 (2002) 1051-1058
9. Ognjanovic S., Bao S., Yamamoto S.Y., Garibay-Tupas J., Samal B., and Bryant-Greenwood G.D. Genomic organization of the gene coding for human pre-B-cell colony enhancing factor and expression in human fetal membranes. J Mol Endocrinol. 26 (2001) 107-117
10. Rongvaux A., Shea R.J., Mulks M.H., Gigot D., Urbain J., Leo O., and Andris F. Pre-B-cell colony-enhancing factor, whose expression is upregulated in activated lymphocytes, is a nicotinamide phosphoribosyltransferase, a cytosolic enzyme involved in NAD biosynthesis. Eur J Immunol. 32 (2002) 3225-3234
11. Kralisch S., Klein J., Lossner U., Bluher M., Paschke R., Stumvoll M., and Fasshauer M. Interleukin-6 is a negative regulator of visfatin gene expression in 3T3-L1 adipocytes. Am J Physiol Endocrinol Metab. 289 (2005) E586-590
12. Haider D.G., Schindler K., Schaller G., Prager G., Wolzt M., and Ludvik B. Increased plasma visfatin concentrations in morbidity obese subjects are reduced after gastric banding. J Clin Endocrinol Metab. 91 (2006) 1578-1581
13. Lopez-Bermejo A., Chico-Julia B., Fernandez-Balsells M., Recasens M., Esteve E., Casamitjana R., Ricart W., and Fernandez-Real J.M. Serum visfatin increases with progressive β-cell deterioration. Diabetes. 55 (2006) 2871-2875
14. Chen M.P., Chung F.M., Chang D.M., Tsai J.C., Huang H.F., Shin S.J., and Lee Y.J. Elevated plasma level of visfatin/pre-B-cell colony-enhancing factor in patients with type 2 diabetes mellitus. J Clin Endocrinol Metab. 91 (2006) 295-299
15. Revollo J.R., Körner A., Mills K.F., Satoh A., Wang T., Garten A., Dasgupta B., Sasaki Y., Wolberger C., Townsend R.R., Milbrandt J., Kiess W., and Imai S. Nampt/PBEF/Visfatin regulates insulin secretion in beta cells as a systemic NAD biosynthetic enzyme. Cell Metab. 6 (2007) 363-375
16. Xie H., Tang S.Y., Luo X.H., Huang J., Cui R.R., Yuan L.Q., Zhou H.D., Wu X.P., and Liao E.Y. Insulin-like effects of visfatin on human osteoblasts. Calcif Tissue Int. 80 (2007) 201-210
17. Cline A.M., Nandar W., Prall B.C., Bowden C.N., and Denbow D.M. Central visfatin causes orexigenic effects in chicks. Behav. Brain Res. 186 (2007) 293-297
18. Krzysik-Walker S.M., Ocon-Grove O.M., Maddineni S.R., Hendricks G.L., and Ramachandran R. Is visfatin an adipokine or myokine? Evidence for greater visfatin expression in skeletal muscle than visceral fat in chickens. Endocrinology. 149 (2008) 1543-1550
19. Griffin H.D., and Goddard C. Rapidly growing broiler (meat-type) chickens: their origin and use for comparative studies of the regulation of growth. Int J Biochem. 26 (1994) 19-28
20. Simon J., Freychet P., and Rosselin G. A study of insulin binding sites in chicken tissues. Diabetologia. 13 (1977) 219-228
21. Seki Y., Sato K., Kono T., Abe H., and Akiba Y. Broiler chickens (Ross strain) lack insulin-responsive glucose transporter GLUT4 and have GLUT8 cDNA. Gen Comp Endocrinol. 133 (2003) 80-87
22. Leveille G.A., O'Hea E.K., and Chakrabarty K. In vivo lipogenesis in the domestic chicken. Proc Soc Exp Biol Med. 128 (1968) 398-401
23. Trayhurn P., and Wusteman M.C. Lipogenesis in genetically diabetic (db/db) mice: developmental changes in brown adipose tissue, white adipose tissue and the liver. Biochim Biophys Acta. 1047 (1990) 168-174
24. Raver N., Taouis M., Dridi S., Derouet M., Simon J., Robinzon B., Djian J., and Gertler A. Large-scale preparation of biologically active recombinant chicken obese protein (leptin). Protein Expr Purif. 14 (1998) 403-408
25. Dridi S., Raver N., Gussakovsky E.E., Derouet M., Picard M., Gertler A., and Taouis M. Biological activities of recombinant chicken leptin C4Sanalog compared with unmodified leptins. Am J Physiol Endocrinol Metab. 279 (2000) E116-123
26. Leclercq B., Blum J.C., and Boyer J.P. Selecting broilers for low or high abdominal fat: initial observations. Br J Poult Sci. 21 (1980) 107-113
27. Feinberg A.P., and Vogelstein B.A. Technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 132 (1983) 6-13
28. -ΔΔCt method. Methods. 25 (2001) 402-408
29. Thompson J.D., Higgins D.G., Gibson T.J., and Clustal .W. improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22 (1994) 4673-4680
30. Tamura K., Dudley J., Nei M., and Kumar S. MEGA 4: Molecular Evolutionary Genetics Analysis (MEGA) software versión 4. 0. Mol Biol Evol 24 (2007) 1596-1599
31. Scheuermann G.N., Bilgili S.F., Hess J.B., and Mulvaney D.R. Breast muscle development in commercial broiler chickens. Poult Sci. 82 (2003) 1648-1658
32. Shinozaki S., Chiba T., Kokame K., Miyata T., Ai M., Kawakami A., Kaneko E., Yoshida M., and Shimokado K. Site-specific effect of estradiol on gene expression in the adipose tissue of ob/ob mice. Horm Metab Res. 39 (2007) 192-196
33. Tullis K.M., Krebs C.J., Leung J.Y., and Robins D.M. The regular of sex-limitation gene rsl enforce male-specific liver gene expression by negative regulation. Endocrinology. 144 (2003) 1854-1860
34. Stephens J.M., and Vidal-Puig A.J. An update on visfatin/pre-B-cell colony enhancing factor, an ubiquitously expressed, illusive cytokine that is regulated in obesity. Curr Opin Lipidol. 17 (2006) 128-131
35. Zhang Y., Proenca R., Maffei M., Barone M., Leopold L., and Friedman J.M. Positional cloning of the mouse obese gene and its human homologue. Nature. 372 (1994) 425-432
36. Lord G. Role of leptin in immunology. Nutr Rev. 60 (2002) S35-38
37. Friedman J.M., and Halaas J.L. Leptin and the regulation of body weight in mammals. Nature 395 (1998) 763-770
38. Dridi S., Dominguez D., and Buyse J. Alzheimer disease: what role for leptin and insulin? Central Nervous System Agents in Medicinal Chemistry. 6 (2006) 271-279
39. Pallett A.L., Morton N.M., Cawthorne M.A., and Emilsson V. Leptin inhibits insulin secretion and reduces insulin mRNA levels in rat isolated pancreatic islets. Biochem Biophys Res Commun. 238 (1997) 267-270
40. Benomar Y., Naour N., Aubourg A., Bailleux V., Gertler A., Djiane J., Guerre-Millo M., and Taouis M. Insulin and leptin induce Glut4 plasma membrane translocation and glucose uptake in a human neuronal cell line by a phosphotidylinositol 3-kinase-dependent mechanism. Endocrinology. 147 (2006) 2550-2556
41. Ohkubo T., Nishio M., Tsurudome M., Ito M., and Ito Y. Structure and tissue distribution of chicken leptin receptor (cOb-R) mRNA. Biochim Biophys Acta. 149 (2000) 303-308
42. Denbow D.M. Food intake control in birds. Neurosci Biobehav Rev. 9 (1985) 223-232
43. Duchamp C., and Barré H. Skeletal muscle as the major site of nonshivering thermogenesis in cold-acclimated duckling. Am J Physiol Regul Integr Comp Physiol. 265 (1993) R10176-10183
44. Friedman-Einat M., Boswell T., Horev G., Girishvarma G., Dunn I.C., Talbot R.T., and Sharp P.J. The chicken leptin gene: has it been cloned? Gen Comp Endocrinol. 115 (1999) 354-363
45. Taouis M., Chen J.W., Daviaud C., Dupont J., Derouet M., and Simon J. Cloning the chicken leptin gene. Gene. 208 (1998) 239-242
46. Ashwell C.M., Czerwinski S.M., Brocht D.M., and McMurtry J.P. Hormonal regulation of leptin expression in broiler chickens. Am J Physiol. 276 (1999) R226-232
47. Sato K., Nishida M., and Akiba Y. Nutritional modulation of leptin messenger RNA in broilers chickens. J Poult Sci. 40 (2003) 13-20
48. Neglia S., Arcamone N., Gargiulo G., and de Girolamo P. Immunocytochemical detection of leptin-like immunoreactivity in the chicken gastroenteric tract. Gen Comp Endocrinol. 155 (2008) 432-437
49. Rao K., Xie J., Yang X., Chen L., Grossmann R., and Zhao R. Maternal low-protein diet programmes offspring growth in association with alterations in yolk leptin deposition and gene expression in yolk-sac membrane, hypothalamus and muscle of developing Langshan chicken embryos. Br J Nutr. 9 (2009) 1-10
50. Kochan Z., Karbowska J., and Meissner W. Leptin is synthesized in the liver and adipose tissue of the dunlin (Calidris alpina). Gen Comp Endocrinol. 148 (2006) 336-339
51. Quillfeldt P., Everaert N., Buyse J., Masello J.F., and Dridi S. Relationship between plasma leptin-like protein levels, begging and provisioning in nestling thin-billed prions Pachyptila belcheri. Gen Comp Endocrinol. 161 (2009) 171-178
52. Adachi H., Takemoto Y., Bungo T., and Ohkubo T. Chicken leptin receptor is functional in activating JAK-STATpathway in vitro. J Endocrinol. 197 (2008) 335-342
53. Hen G., Yosefi S., Ronin A., Einat P., Rosenblum C.I., Denver R.J., and Friedman-Einat M. Monitoring leptin activity using the chicken leptin receptor. J Endocrinol. 197 (2008) 325-333
54. Dridi S., Swennen Q., Decuypere E., and Buyse J. Mode of leptin action in chicken hypothalamus. Brain Res. 1047 (2005) 214-223
55. Dridi S., Buyse J., Decuypere E., and Taouis M. Potential role of leptin in increase of fatty acid synthase gene expression in chicken liver. Domest Anim Endocrinol. 29 (2005) 646-660
56. Dridi S., Ververken C., Hillgartner F.B., Arckens L., Vander Gucht E., Cnops L., Decuypere E., and Buyse J. FAS inhibitor cerulenin reduces food intake and melanocortin receptor gene expression without modulating the other (an)orexigenic neuropeptides in chickens. Am J Physiol Regul Integr Comp Physiol. 29 (2006) R138-147
57. Loftus T.M., Jaworsky D.E., Frehywot G.L., Townsend C.A., Ronnett G.V., Lane M.D., and Kuhajda F.P. Reduced food intake and body weight in mice treated with fatty acid synthase inhibitors. Science. 288 (2000) 2379-2381
58. Yang H., Yang T., Baur J.A., Perez E., Matsui T., Carmona J.J., Lamming D.W., Souza-Pinto N.C., Bohr V.A., Rosenzweig A., De Cabo R., Sauve A.A., and Sinclair D.A. Nutrient-sensitive mitochondrial NAD+ levels dictate cell survival. Cell. 130 (2007) 1095-1107