Previous studies indicate that Chinese indigenous pig breeds demonstrate distinct pattern of glucocorticoid receptor (GR) expression, which is associated with their unique growth and metabolic phenotypes. Here we sought to unravel the transcriptional mechanisms underlying the breed-specific hepatic GR expression in preweaning Chinese Erhualian (EHL) and Western Large White (LW) piglets. Total GR mRNA and the predominant GR mRNA variant 1–9/10 were expressed significantly higher in EHL compared with LW piglets (P<0.01), which was associated with more enriched histone H3 acetylation on 1–9/10 promoter (P<0.05). Nuclear content of transcription factor specificity protein 1 (Sp1) was significantly lower in EHL piglets, yet its binding to GR 1–9/10 promoter was significantly higher in EHL piglets, as revealed by chromatin immunoprecipitation assays. Although p53 binding to GR promoter 1–9/10 did not differ between breeds, expression of p53 mRNA and protein, as well as its binding to Sp1, were significantly higher in EHL piglets. Moreover, p53 activator doxorubicin significantly enhanced GR 1–9/10 promoter activity in HepG2 cells at 100 nM, which was associated with significantly higher protein content of p53 and GR. Sp1 inhibitor, mithramycin A, significantly inhibited (P<0.05) the basal activity of GR promoter 1–9/10 and completely blocked doxorubicin -induced activation of GR promoter 1–9/10. These data indicate that higher hepatic GR expression in EHL piglets attributes mainly to the enhanced transcription of GR promoter 1–9/10, which is achieved from breed-specific interaction of p53 and Sp1 on porcine GR 1–9/10 promoter.
References
[1]
Bamberger CM, Schulte HM, Chrousos GP (1996) Molecular determinants of glucocorticoid receptor function and tissue sensitivity to glucocorticoids. Endocr Rev 17: 245–261.
[2]
Lu NZ, Cidlowski JA (2004) The origin and functions of multiple human glucocorticoid receptor isoforms. Ann N Y Acad Sci 1024: 102–123.
[3]
Poletto R, Steibel JP, Siegford JM, Zanella AJ (2006) Effects of early weaning and social isolation on the expression of glucocorticoid and mineralocorticoid receptor and 11beta-hydroxysteroid dehydrogenase 1 and 2 mRNAs in the frontal cortex and hippocampus of piglets. Brain Res 1067: 36–42.
[4]
Li LA, Xia D, Bao ED, Wei S, Xiao JS, et al. (2008) Erhualian and Pietrain pigs exhibit distinct behavioral, endocrine and biochemical responses during transport. Livest Sci 113: 169–177.
[5]
Wei S, Xia D, Li L, Xiao J, Bao J, et al. (2010) Breed-specific expression of hippocampal 11[beta]-hydroxysteroid dehydrogenases and glucocorticoid receptors in Erhualian and Pietrain pigs exhibiting distinct stress coping characteristics. Livest Sci 131: 240–244.
[6]
Yang X, Liu R, Elke A, Dong X, Zhao R (2012) Breed-specific patterns of hepatic gluconeogenesis and glucocorticoid action in pigs. Archiv Tierzucht 1: 152–162.
[7]
Li X, Yang X, Shan B, Shi J, Xia D, et al. (2009) Meat quality is associated with muscle metabolic status but not contractile myofiber type composition in premature pigs. Meat Sci 81: 218–223.
[8]
Turner JD, Alt SR, Cao L, Vernocchi S, Trifonova S, et al. (2010) Transcriptional control of the glucocorticoid receptor: CpG islands, epigenetics and more. Biochem Pharmacol 80: 1860–1868.
[9]
Cao-Lei L, Leija SC, Kumsta R, Wust S, Meyer J, et al. (2011) Transcriptional control of the human glucocorticoid receptor: identification and analysis of alternative promoter regions. Hum Genet 129: 533–543.
[10]
Strahle U, Schmidt A, Kelsey G, Stewart AF, Cole TJ, et al. (1992) At least three promoters direct expression of the mouse glucocorticoid receptor gene. Proc Natl Acad Sci U S A 89: 6731–6735.
[11]
Russcher H, Dalm VA, de Jong FH, Brinkmann AO, Hofland LJ, et al. (2007) Associations between promoter usage and alternative splicing of the glucocorticoid receptor gene. J Mol Endocrinol 38: 91–98.
[12]
McCormick JA, Lyons V, Jacobson MD, Noble J, Diorio J, et al. (2000) 5′-heterogeneity of glucocorticoid receptor messenger RNA is tissue specific: differential regulation of variant transcripts by early-life events. Mol Endocrinol 14: 506–517.
[13]
Kanitz E, Otten W, Hameister T, Tuchscherer M, Puppe B, et al. (2011) Age-related changes in corticosteroid receptor expression and monoamine neurotransmitter concentrations in various brain regions of postnatal pigs. J Neurosci 89: 1134–1141.
[14]
Jenson M, Kilroy G, York DA, Braymer D (1996) Abnormal regulation of hepatic glucocorticoid receptor mRNA and receptor protein distribution in the obese Zucker rat. Obes Res 4: 133–143.
[15]
Marelli SP, Terova G, Cozzi MC, Lasagna E, Sarti FM, et al. (2010) Gene expression of hepatic glucocorticoid receptor NR3C1 and correlation with plasmatic corticosterone in Italian chickens. Anim Biotechnol 21: 140–148.
[16]
Suehiro T, Kaneda T, Ikeda Y, Arii K, Kumon Y, et al. (2004) Regulation of human glucocorticoid receptor gene transcription by Sp1 and p53. Mol Cell Endocrinol 222: 33–40.
[17]
Breslin MB, Vedeckis WV (1998) The human glucocorticoid receptor promoter upstream sequences contain binding sites for the ubiquitous transcription factor, Yin Yang 1. J Steroid Biochem 67: 369–381.
[18]
Govindan MV (2010) Recruitment of cAMP-response element-binding protein and histone deacetylase has opposite effects on glucocorticoid receptor gene transcription. J Biol Chem 285: 4489–4510.
[19]
Weaver IC, Cervoni N, Champagne FA, D'Alessio AC, Sharma S, et al. (2004) Epigenetic programming by maternal behavior. Nat Neurosci 7: 847–854.
[20]
Nobukuni Y, Smith CL, Hager GL, tera-Wadleigh SD (1995) Characterization of the human glucocorticoid receptor promoter. Biochemistry 34: 8207–8214.
[21]
Koutsodontis G, Vasilaki E, Chou WC, Papakosta P, Kardassis D (2005) Physical and functional interactions between members of the tumour suppressor p53 and the Sp families of transcription factors: importance for the regulation of genes involved in cell-cycle arrest and apoptosis. Biochem J 389: 443–455.
[22]
Velculescu VE, El-Deiry WS (1996) Biological and clinical importance of the p53 tumor suppressor gene. Clin Chem 42: 858–868.
[23]
Sengupta S, Wasylyk B (2004) Physiological and pathological consequences of the interactions of the p53 tumor suppressor with the glucocorticoid, androgen, and estrogen receptors. Ann N Y Acad Sci 1024: 54–71.
[24]
Nishimura K, Makino S, Tanaka Y, Kaneda T, Hashimoto K (2004) Altered expression of p53 mRNA in the brain and pituitary during repeated immobilization stress: negative correlation with glucocorticoid receptor mRNA levels. J Neuroendocrinol 16: 84–91.
[25]
Murphy SH, Suzuki K, Downes M, Welch GL, De Jesus P, et al. (2011) Tumor suppressor protein (p)53, is a regulator of NF-kappaB repression by the glucocorticoid receptor. Proc Natl Acad Sci U S A 108: 17117–17122.
[26]
Reyer H, Ponsuksili S, Wimmers K, Murani E (2013) Transcript variants of the porcine glucocorticoid receptor gene (NR3C1). Gen Comp Endocrinol 189: 127–133.
[27]
Zou H, Li R, Jia Y, Yang X, Ni Y, et al. (2012) Breed-Dependent Transcriptional Regulation of 5′-Untranslated GR (NR3C1) Exon 1 mRNA Variants in the Liver of Newborn Piglets. PLoS One 7: e40432.
[28]
Lee JS, Ward WO, Knapp G, Ren H, Vallanat B, et al. (2012) Transcriptional ontogeny of the developing liver. BMC Genomics 13: 33.
[29]
FELDMAN D (1974) Ontogeny of Rat Hepatic Glucocorticoid Receptors. Endocrinology 95: 1219–1227.
[30]
Kitraki E, Alexis MN, Stylianopoulou F (1984) Glucocorticoid receptors in developing rat brain and liver. J Steroid Biochem 20: 263–269.
[31]
Kalinyak JE, Griffin CA, Hamilton RW, Bradshaw JG, Perlman AJ, et al. (1989) Developmental and hormonal regulation of glucocorticoid receptor messenger RNA in the rat. J Clin Invest 84: 1843–1848.
[32]
McNeil CJ, Nwagwu MO, Finch AM, Page KR, Thain A, et al. (2007) Glucocorticoid exposure and tissue gene expression of 11beta HSD-1, 11beta HSD-2, and glucocorticoid receptor in a porcine model of differential fetal growth. Reproduction 133: 653–661.
[33]
Saffer JD, Jackson SP, Annarella MB (1991) Developmental expression of Sp1 in the mouse. Molecular and Cellular Biology 11: 2189–2199.
[34]
Kaczynski J, Cook T, Urrutia R (2003) Sp1- and Kruppel-like transcription factors. Genome Biol 4: 206.
[35]
Zong J, Ashraf J, Thompson EB (1990) The promoter and first, untranslated exon of the human glucocorticoid receptor gene are GC rich but lack consensus glucocorticoid receptor element sites. Mol Cell Biol 10: 5580–5585.
[36]
Berger SL (2002) Histone modifications in transcriptional regulation. Curr Opin Genet Dev 12: 142–148.
[37]
Shahbazian MD, Grunstein M (2007) Functions of Site-Specific Histone Acetylation and Deacetylation. Annu Rev Biochem 76: 75–100.
[38]
Yamabe Y, Shimamoto A, Goto M, Yokota J, Sugawara M, et al. (1998) Sp1-Mediated Transcription of the Werner Helicase Gene Is Modulated by Rb and p53. Mol Cell Biol 18: 6191–6200.
[39]
D'Alessio JA, Ng R, Willenbring H, Tjian R (2011) Core promoter recognition complex changes accompany liver development. Proc Natl Acad Sci U S A 108: 3906–3911.
[40]
Chua H-H, Chiu H-Y, Lin S-J, Weng P-L, Lin J-H, et al. (2012) p53 and Sp1 cooperate to regulate the expression of epstein–barr viral Zta protein. Journal of Medical Virology 84: 1279–1288.
[41]
Dhar SK, Xu Y, Chen Y, St Clair DK (2006) Specificity protein 1-dependent p53-mediated suppression of human manganese superoxide dismutase gene expression. J Biol Chem 281: 21698–21709.
[42]
Thornborrow EC, Manfredi JJ (2001) The Tumor Suppressor Protein p53 Requires a Cofactor to Activate Transcriptionally the Human BAX Promoter. J Biol Chem 276: 15598–15608.
[43]
Zhan Q, Chen IT, Antinore MJ, Fornace AJ Jr (1998) Tumor suppressor p53 can participate in transcriptional induction of the GADD45 promoter in the absence of direct DNA binding. Mol Cell Biol 18: 2768–2778.
[44]
Sadji-Ouatas Z, Lasfer M, Julien S, Feldmann G, Reyl-Desmars F (2002) Doxorubicin and octreotide induce a 40 kDa breakdown product of p53 in human hepatoma and tumoral colon cell lines. Biochem J 364: 881–885.
[45]
Koblish HK, Zhao S, Franks CF, Donatelli RR, Tominovich RM, et al. (2006) Benzodiazepinedione inhibitors of the Hdm2:p53 complex suppress human tumor cell proliferation in vitro and sensitize tumors to doxorubicin in vivo. Mol Cancer Ther 5: 160–169.
[46]
Ju J, Schmitz JC, Song B, Kudo K, Chu E (2007) Regulation of p53 Expression in Response to 5-Fluorouracil in Human Cancer RKO Cells. Clin Cancer Res 13: 4245–4251.
[47]
Wang S, Song P, Zou M-H (2012) Inhibition of AMP-activated Protein Kinase α (AMPKα) by Doxorubicin Accentuates Genotoxic Stress and Cell Death in Mouse Embryonic Fibroblasts and Cardiomyocytes. J Biol Chem 287: 8001–8012.
[48]
Rudiger JJ, Roth M, Bihl MP, Cornelius BC, Johnson M, et al. (2002) Interaction of C/EBPalpha and the glucocorticoid receptor in vivo and in nontransformed human cells. FASEB J 16: 177–184.
[49]
Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25: 402–408.
[50]
Alastalo TP, Hellesuo M, Sandqvist A, Hietakangas V, Kallio M, et al. (2003) Formation of nuclear stress granules involves HSF2 and coincides with the nucleolar localization of Hsp70. J Cell Sci 116: 3557–3570.
[51]
Cha JY, Repa JJ (2007) The liver X receptor (LXR) and hepatic lipogenesis. The carbohydrate-response element-binding protein is a target gene of LXR. J Biol Chem 282: 743–751.
[52]
Ming L, Sakaida T, Yue W, Jha A, Zhang L, et al. (2008) Sp1 and p73 activate PUMA following serum starvation. Carcinogenesis 29: 1878–1884.
[53]
Singh DP, Bhargavan B, Chhunchha B, Kubo E, Kumar A, et al. (2012) Transcriptional protein Sp1 regulates LEDGF transcription by directly interacting with its cis-elements in GC-rich region of TATA-less gene promoter. PLoS One 7: e37012.
[54]
Kataoka H, Bonnefin P, Vieyra D, Feng X, Hara Y, et al. (2003) ING1 Represses Transcription by Direct DNA Binding and through Effects on p53. Cancer Res 63: 5785–5792.
[55]
Iwano S, Shibahara N, Saito T, Kamataki T (2006) Activation of p53 as a causal step for atherosclerosis induced by polycyclic aromatic hydrocarbons. FEBS Lett 580: 890–893.