Abstract
The polyglutamine tract, beginning at codon 75 in the N-terminal modulatory domain of rat glucocorticoid receptor (rGR), was analyzed in 61 inbred strains and 155 wild caught Rattus norvegicns. A discontinuous distribution of repeat lengths was found (7, 17–23 repeats). To investigate the possible significance of this distribution, full-length rGR cDNAs with 7, 18, 20, and 21 CAG repeats were expressed in CV-1 cells, and the resulting GR protein analyzed by Western blots and extensive Scatchard analyses. The quantity and steroid binding capacity of GR, together with the binding affinities for dexamethasone and corticosterone, were found to be indistinguishable for the four repeat alleles. From the sequencing of four inbred strains CAG repeat variants were found to be flanked by silent allelic substitutions at nucleotide positions 198, 531, and 711. The four variable sites extended over 471–519 bp of coding sequence, forming six Grl haplotypes. The results are discussed in the light of genetic studies on the Milan hypertensive and normotensive strains of rat. Codon sequence of rat GR required amendment at the following residues: D98, G226, D260, P600, and F602.
Similar content being viewed by others
References
Almlöf A, Wright APH, Gustafsson J-A (1995) Role of acidic and phosphorylated residues in gene activation by the GR. J Biol Chem 270, 17535–17540
Almlöf T, Gustafsson J-A, Wright APH (1997) Role of hydrophobic amino acid clusters in the transactivation activity of the human glucocorticoid receptor. Mol Cell Biol 17, 934–945
Bianchi G, Ferrari P, Barker BR (1984) The Milan hypertensive strain. In Handbook of Hypertension, W de Jong, (ed.) (Amsterdam: Elsevier publishers) 4, pp. 328–349
Bianchi G, Ferrari P, Salvati P, Parenti P, Cusi D, Guidi E (1986) A renal abnormality in the Milan hypertensive strain of rats and in humans predisposed to essential hypertension. Hypertension 4 (Suppl 3), S33-S36
Brook DJ, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, Hunter K, Stanton VP, Thirion J-P, Hudson T, Sohn R, Zemelman B, Snell RG, Rundle SA, Crow S, Davies J, Shelbourne P, Buxton J, Jones C, Juvonen V, Johnson K, Harper PS, Shaw DJ, Housman DE (1992) Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 68, 799–808
Chamberlain NL, Driver ED, Miesfeld RL (1994) The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function. Nucleic Acids Res 22, 3181–3186
Coleman MP, Murray JC, Willard HF, Nolan KF, Reid KBM, Beake DJ, Lindsay S, Bhattacharya SS, Wright A, Davies KE (1991) Genetic and physical mapping around the properidin P gene. Genomics 11, 991–996
Danielsen M (1991) Structure and function of the glucocorticoid receptor. In Nuclear Hormone Receptors M Parker, (ed) (Suffolk, UK: St. Edmunsbury Press, Ltd.), pp 39–68
Edwards A, Hammond HA, Jin L, Casky TC, Chakraborty R (1992) Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics 12, 241–253
Ferrari P, Mantero F, Bianchi G (1985) Role of adrenal steroids in the rat genetic models of hypertension. In The Adrenal Gland and Hypertension, F Mantero, E Biglieri, JW Funder, BJ Scoggins, (eds) (New York: Raven Press), Serono Symposia 27, pp 149–158
Fraser R, Ancil WK, Brown WB, Ingram MC, Holloway CD, Henderson IW, Kenyon CJ (1994) Evidence of abnormalities in corticosteroid secretion, leading to volume-dependent hypertension in Milan rats. Hypertension 24, 512–515
Fu Y-H, Kuhl DPA, Pizzuti A, Pieretti M, Sutclife JF, Richards S, Verkerk AJMH, Holden JJA, Fenwick Jr, RG, Waren ST, Oostra BA, Nelson DL and Casky CT (1991) Variation of the CGG repeat of the Fragile X site results in genetic instability: resolution of the Sherman paradox. Cell 67, 1047–1058
Gearing KL, Gustafsson J-A, Okret S (1993) Heterogeneity in the polyglutamine tract of the glucocorticoid receptor from different rat strains. Nucleic Acids Res 21, 2014
Greenhouse DD, Festing MFW, Hasans S, Cohen AL (1990) Catalogue of inbred strains of rats. In Genetic Monitoring of Inbred Strains of Rats HJ Hedrich (ed) (Stuttgart: Gustav Fischer Verlag), pp 410–480
Harris S, Moncrieff C, Johnson K (1996) Myotonic dystrophy: will the real gene please step forward! Hum Mol Genet 5, 1417–1423
Hedrich HJ (1990) List of congenic and segregating inbred strains. In Genetic Monitoring of Inbred Strains of Rats, HJ Hedrich (ed) (Stuttgart: Gustav Fischer Verlag), pp 481–486
Heeley RP, Gill E, VanZutphen B, Kenyon CJ, Sutcliffe RG (1996a) A bimodal distribution of CAG repeats in the glucocorticoid receptor of wild and inbred rats. J Endocrinol 148 (Suppl)
Heeley RP, Casari G, Zagato L, Torielli L, Sutcliffe RG, Bianchi G, Kenyon CJ (1996b) Glucocorticoid receptor mutations in genetically hypertensive rats: markers of glucocorticoid sensitivity. Biochem Soc Trans 25, 236S
Hollenberg SM, Evans RM (1988) Multiple and cooperative transactivation domains of the human glucocorticoid receptor. Cell 55, 899–906
Housely PR, Sanchez ER, Danielsen M, Ringold GM, Pratt WB (1990) Evidence that the conserved region in the steroid binding domain of the glucocorticoid receptor is required for both optimal binding of HSP90 and protection from proteolytic cleavage: a two site model for HSP90 binding to the hormone binding domain. J Biol Chem 265, 12778–12781
Iniguez-Lluhi JA, Lou DY, Yamamoto KR (1997) Three amino acid substitutions selectively disrupt the activation but not the repression function of the glucocorticoid receptor N-terminus. J Biol Chem 272, 4149–4156
Jacob HJ, Brown DM, Bunker RK, Daly MJ, Dzau VJ, Goodman A, Koike G, Kren V, Kurtz T, Lernmark A, Levan G, Mao Y-p, Petersson A, Pravenec M, Simon JS, Szpirer C, Szpirer J, Trolliet MR, Winer ES, Lander ES (1995) A linkage map of the laboratory rat. Nat Genet 9, 63–69
Kashi Y, King D, Soller M (1997) Simple sequence repeats as a source of quantitative genetic variation. Trends-Genet 13, 74–78
Kenyon CJ, Casari G, Zagato L, Inglis G, Heeley R, Torielli L, Connell JMC, Sutcliffe RG, Bianchi G (1994) Glucocorticoid receptor and 11β-hydroxylase genes interact epistatically with adducin in blood pressure control of Milan rats. J Endocrinol 143 (suppl), xx-xx
LaSpada AR, Roling DB, Harding AE, Warner CL, Spiegel R, Hausmanowa-Petrusewics I, Yee W-C, Fischbeck AH (1992) Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Nat Genet 197, 301–304
Lubahn DB, Joseph DR, Sar M, Tan J-a, Higgs HN, Larson RE, French FS, Wilson EM (1988) The human androgen receptor: complementary deoxyribonucleic acid cloning, sequence analysis and gene expression in prostate. Mol Endocrinol 2, 1265–1275
McPhaul MJ, Marcelli M, Tilley WD, Griffin JE, Isidro-Gutierrez RF, Wilson JD (1991) Molecular basis of androgen resistance in a family with a qualitative abnormality of the androgen receptor and responsive to high dose androgen therapy. J Clin Invest 87, 1413–1421
Mhatre AN, Trifiro MA, Kaufman M, Kazemi-Esfarjani P, Figlewics D, Rouleou G, Pinsky L (1993) Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy. Nat Genet 5, 184–188
Miesfeld R, Rusconi S, Godowski P, Maler BA, Okret S, Wikström A-C, Gustafsson J-A, Yamamoto KR (1986) Genetic complementation of glucocorticoid receptor deficiency by expression of cloned receptor cDNA. Cell 46, 389–399
Miesfeld R, Godowski PJ, Maler BA, Yamamoto KR (1987) Glucocorticoid receptor mutants that define a small region sufficient for enhancer activation. Science 236, 423–427
Munson PJ, Rodbard D (1980) Versatile computerised approach for characterisation of ligand binding systems. Anal Biochem 107, 220–239
Otsen M (1995) Use of DNA markers for genetic characterisation and linkage studies in the rat. PhD. Thesis, Utrecht University, pp 43–58
Panarelli M, Holloway CD, Barr ABP, Fraser R, Kenyon CJ (1995) Differences in temperature sensitive receptor binding of glucocorticoids in Spontaneously Hypertensive (SHR) and Wistar Kyoto (WKY) rats. Steroids 60, 73–75
Perutz MF, Johnson T, Suzuki M, Finch JT (1994) Glutamine repeats as polar zippers: their possible role in neurodegenerative diseases. Proc Natl Acad Sci 91, 5355–5358
Ross CA, McInnis MG, Margolis RL, Li S-H (1993) Genes with triplet repeats: candidate mediators of neuropsychiatric disorders. Trends Neurosci 16, 254–260
Rubinsztein DC, Amos W, Leggo J, Goodurn S, Jain S, Li S-H, Margolis RL, Ross CA, Ferguson-Smith MA (1995) Microsatellite evolution—evidence for directionality and variation in rate between species. Nat Genet 10, 337–343
Schoenberg MP, Hakimi JM, Wang S, Bova GS, Epstein GI, Fischbeck KH, Isaacs WB, Walsh PC, Barrack ER (1994) Microsatellite mutation (CAG24–18) in the androgen receptor gene in human prostate cancer. Biochem Biophys Res Commun 198, 74–80
Sinden SS, Wells WRD (1992) DNA structure, mutations and human genetic disease. Curr Opin Biotechnol 3, 612–622
Stewart PM, Whorwood CB, Valentino R, Burt D, Sheppard MC, Edwards CRW (1993) 11 β-hydroxysteroid dehydrogenase activity and gene expression in the hypertensive Bianchi Milan rat. Hypertension 11, 349–354
Zerylnick C, Torroni A, Sherman SL, Warren ST (1995) Normal variation at the myotonic dystrophy locus in global human populations. Am J Hum Genet 56, 123–130
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Heeley, R.P., Gill, E., van Zutphen, B. et al. Polymorphisms of the glucocorticoid receptor gene in laboratory and wild rats: steroid binding properties of trinucleotide CAG repeat length variants. Mammalian Genome 9, 198–203 (1998). https://doi.org/10.1007/s003359900725
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/s003359900725