Skip to main content
The EMBO Journal logoLink to The EMBO Journal
. 1996 Jun 17;15(12):3006–3015.

Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: evidence for tissue-specific modulation of receptor function.

D Forrest 1, E Hanebuth 1, R J Smeyne 1, N Everds 1, C L Stewart 1, J M Wehner 1, T Curran 1
PMCID: PMC450242  PMID: 8670802

Abstract

The diverse functions of thyroid hormone (T3) are presumed to be mediated by two genes encoding the related receptors, TRalpha and TRbeta. However, the in vivo functions of TRalpha and TRbeta are undefined. Here, we report that targeted inactivation of the mouse TRbeta gene results in goitre and elevated levels of thyroid hormone. Also, thyroid-stimulating hormone (TSH), which is released by pituitary thyrotropes and which is normally suppressed by increased levels of thyroid hormone, was present at elevated levels in homozygous mutant (Thrb-/-) mice. These findings suggest a unique role for TRbeta that cannot be substituted by TRalpha in the T3-dependent feedback regulation of TSH transcription. Thrb-/- mice provide a recessive model for the human syndrome of resistance to thyroid hormone (RTH) that exhibits a similar endocrine disorder but which is typically caused by dominant TRbeta mutants that are transcriptional inhibitors. It is unknown whether TRalpha, TRbeta or other receptors are targets for inhibition in dominant RTH; however, the analysis of Thrb-/- mice suggests that antagonism of TRbeta-mediated pathways underlies the disorder of the pituitary-thyroid axis. Interestingly, in the brain, the absence of TRbeta may not mimic the defects often associated with dominant RTH, since no overt behavioural or neuroanatomical abnormalities were detected in Thrb-/- mice. These data define in vivo functions for TRbeta and indicate that specificity in T3 signalling is conferred by distinct receptor genes.

Full text

PDF
3006

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anthony A., Adams P. M., Stein S. A. The effects of congenital hypothyroidism using the hyt/hyt mouse on locomotor activity and learned behavior. Horm Behav. 1993 Sep;27(3):418–433. doi: 10.1006/hbeh.1993.1031. [DOI] [PubMed] [Google Scholar]
  2. Baniahmad A., Tsai S. Y., O'Malley B. W., Tsai M. J. Kindred S thyroid hormone receptor is an active and constitutive silencer and a repressor for thyroid hormone and retinoic acid responses. Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10633–10637. doi: 10.1073/pnas.89.22.10633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bradley D. J., Towle H. C., Young W. S., 3rd Spatial and temporal expression of alpha- and beta-thyroid hormone receptor mRNAs, including the beta 2-subtype, in the developing mammalian nervous system. J Neurosci. 1992 Jun;12(6):2288–2302. doi: 10.1523/JNEUROSCI.12-06-02288.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brönnegård M., Törring O., Bös J., Sylven C., Marcus C., Wallin G. Expression of thyrotropin receptor and thyroid hormone receptor messenger ribonucleic acid in normal, hyperplastic, and neoplastic human thyroid tissue. J Clin Endocrinol Metab. 1994 Aug;79(2):384–389. doi: 10.1210/jcem.79.2.8045952. [DOI] [PubMed] [Google Scholar]
  5. Chambon P. The retinoid signaling pathway: molecular and genetic analyses. Semin Cell Biol. 1994 Apr;5(2):115–125. doi: 10.1006/scel.1994.1015. [DOI] [PubMed] [Google Scholar]
  6. Chatterjee V. K., Lee J. K., Rentoumis A., Jameson J. L. Negative regulation of the thyroid-stimulating hormone alpha gene by thyroid hormone: receptor interaction adjacent to the TATA box. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9114–9118. doi: 10.1073/pnas.86.23.9114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chatterjee V. K., Nagaya T., Madison L. D., Datta S., Rentoumis A., Jameson J. L. Thyroid hormone resistance syndrome. Inhibition of normal receptor function by mutant thyroid hormone receptors. J Clin Invest. 1991 Jun;87(6):1977–1984. doi: 10.1172/JCI115225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chen J. D., Evans R. M. A transcriptional co-repressor that interacts with nuclear hormone receptors. Nature. 1995 Oct 5;377(6548):454–457. doi: 10.1038/377454a0. [DOI] [PubMed] [Google Scholar]
  9. Childs G. V., Taub K., Jones K. E., Chin W. W. Triiodothyronine receptor beta-2 messenger ribonucleic acid expression by somatotropes and thyrotropes: effect of propylthiouracil-induced hypothyroidism in rats. Endocrinology. 1991 Nov;129(5):2767–2773. doi: 10.1210/endo-129-5-2767. [DOI] [PubMed] [Google Scholar]
  10. Chin W. W., Kronenberg H. M., Dee P. C., Maloof F., Habener J. F. Nucleotide sequence of the mRNA encoding the pre-alpha-subunit of mouse thyrotropin. Proc Natl Acad Sci U S A. 1981 Sep;78(9):5329–5333. doi: 10.1073/pnas.78.9.5329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Damm K., Thompson C. C., Evans R. M. Protein encoded by v-erbA functions as a thyroid-hormone receptor antagonist. Nature. 1989 Jun 22;339(6226):593–597. doi: 10.1038/339593a0. [DOI] [PubMed] [Google Scholar]
  12. Fondell J. D., Roy A. L., Roeder R. G. Unliganded thyroid hormone receptor inhibits formation of a functional preinitiation complex: implications for active repression. Genes Dev. 1993 Jul;7(7B):1400–1410. doi: 10.1101/gad.7.7b.1400. [DOI] [PubMed] [Google Scholar]
  13. Forrest D., Hallbök F., Persson H., Vennström B. Distinct functions for thyroid hormone receptors alpha and beta in brain development indicated by differential expression of receptor genes. EMBO J. 1991 Feb;10(2):269–275. doi: 10.1002/j.1460-2075.1991.tb07947.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Forrest D., Sjöberg M., Vennström B. Contrasting developmental and tissue-specific expression of alpha and beta thyroid hormone receptor genes. EMBO J. 1990 May;9(5):1519–1528. doi: 10.1002/j.1460-2075.1990.tb08270.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Forrest D. The erbA/thyroid hormone receptor genes in development of the central nervous system. Semin Cancer Biol. 1994 Apr;5(2):167–176. [PubMed] [Google Scholar]
  16. Forrest D., Yuzaki M., Soares H. D., Ng L., Luk D. C., Sheng M., Stewart C. L., Morgan J. I., Connor J. A., Curran T. Targeted disruption of NMDA receptor 1 gene abolishes NMDA response and results in neonatal death. Neuron. 1994 Aug;13(2):325–338. doi: 10.1016/0896-6273(94)90350-6. [DOI] [PubMed] [Google Scholar]
  17. Geyer M. A., Wilkinson L. S., Humby T., Robbins T. W. Isolation rearing of rats produces a deficit in prepulse inhibition of acoustic startle similar to that in schizophrenia. Biol Psychiatry. 1993 Sep 15;34(6):361–372. doi: 10.1016/0006-3223(93)90180-l. [DOI] [PubMed] [Google Scholar]
  18. Gurr J. A., Catterall J. F., Kourides I. A. Cloning of cDNA encoding the pre-beta subunit of mouse thyrotropin. Proc Natl Acad Sci U S A. 1983 Apr;80(8):2122–2126. doi: 10.1073/pnas.80.8.2122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Hauser P., Zametkin A. J., Martinez P., Vitiello B., Matochik J. A., Mixson A. J., Weintraub B. D. Attention deficit-hyperactivity disorder in people with generalized resistance to thyroid hormone. N Engl J Med. 1993 Apr 8;328(14):997–1001. doi: 10.1056/NEJM199304083281403. [DOI] [PubMed] [Google Scholar]
  20. Hodin R. A., Lazar M. A., Wintman B. I., Darling D. S., Koenig R. J., Larsen P. R., Moore D. D., Chin W. W. Identification of a thyroid hormone receptor that is pituitary-specific. Science. 1989 Apr 7;244(4900):76–79. doi: 10.1126/science.2539642. [DOI] [PubMed] [Google Scholar]
  21. Hörlein A. J., När A. M., Heinzel T., Torchia J., Gloss B., Kurokawa R., Ryan A., Kamei Y., Söderström M., Glass C. K. Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor. Nature. 1995 Oct 5;377(6548):397–404. doi: 10.1038/377397a0. [DOI] [PubMed] [Google Scholar]
  22. Kendall S. K., Gordon D. F., Birkmeier T. S., Petrey D., Sarapura V. D., O'Shea K. S., Wood W. M., Lloyd R. V., Ridgway E. C., Camper S. A. Enhancer-mediated high level expression of mouse pituitary glycoprotein hormone alpha-subunit transgene in thyrotropes, gonadotropes, and developing pituitary gland. Mol Endocrinol. 1994 Oct;8(10):1420–1433. doi: 10.1210/mend.8.10.7531821. [DOI] [PubMed] [Google Scholar]
  23. Lechan R. M., Qi Y., Jackson I. M., Mahdavi V. Identification of thyroid hormone receptor isoforms in thyrotropin-releasing hormone neurons of the hypothalamic paraventricular nucleus. Endocrinology. 1994 Jul;135(1):92–100. doi: 10.1210/endo.135.1.7516871. [DOI] [PubMed] [Google Scholar]
  24. Lee J. W., Ryan F., Swaffield J. C., Johnston S. A., Moore D. D. Interaction of thyroid-hormone receptor with a conserved transcriptional mediator. Nature. 1995 Mar 2;374(6517):91–94. doi: 10.1038/374091a0. [DOI] [PubMed] [Google Scholar]
  25. Lezoualc'h F., Hassan A. H., Giraud P., Loeffler J. P., Lee S. L., Demeneix B. A. Assignment of the beta-thyroid hormone receptor to 3,5,3'-triiodothyronine-dependent inhibition of transcription from the thyrotropin-releasing hormone promoter in chick hypothalamic neurons. Mol Endocrinol. 1992 Nov;6(11):1797–1804. doi: 10.1210/mend.6.11.1480171. [DOI] [PubMed] [Google Scholar]
  26. Marks M. J., Stitzel J. A., Collins A. C. Genetic influences on nicotine responses. Pharmacol Biochem Behav. 1989 Jul;33(3):667–678. doi: 10.1016/0091-3057(89)90406-1. [DOI] [PubMed] [Google Scholar]
  27. Mellström B., Naranjo J. R., Santos A., Gonzalez A. M., Bernal J. Independent expression of the alpha and beta c-erbA genes in developing rat brain. Mol Endocrinol. 1991 Sep;5(9):1339–1350. doi: 10.1210/mend-5-9-1339. [DOI] [PubMed] [Google Scholar]
  28. Nagaya T., Jameson J. L. Thyroid hormone receptor dimerization is required for dominant negative inhibition by mutations that cause thyroid hormone resistance. J Biol Chem. 1993 Jul 25;268(21):15766–15771. [PubMed] [Google Scholar]
  29. Ng L., Forrest D., Haugen B. R., Wood W. M., Curran T. N-terminal variants of thyroid hormone receptor beta: differential function and potential contribution to syndrome of resistance to thyroid hormone. Mol Endocrinol. 1995 Sep;9(9):1202–1213. doi: 10.1210/mend.9.9.7491112. [DOI] [PubMed] [Google Scholar]
  30. Ono S., Schwartz I. D., Mueller O. T., Root A. W., Usala S. J., Bercu B. B. Homozygosity for a dominant negative thyroid hormone receptor gene responsible for generalized resistance to thyroid hormone. J Clin Endocrinol Metab. 1991 Nov;73(5):990–994. doi: 10.1210/jcem-73-5-990. [DOI] [PubMed] [Google Scholar]
  31. Pauly J. R., Robinson S. F., Collins A. C. Chronic corticosterone administration enhances behavioral sensitization to amphetamine in mice. Brain Res. 1993 Aug 27;620(2):195–202. doi: 10.1016/0006-8993(93)90156-h. [DOI] [PubMed] [Google Scholar]
  32. Prost E., Koenig R. J., Moore D. D., Larsen P. R., Whalen R. G. Multiple sequences encoding potential thyroid hormone receptors isolated from mouse skeletal muscle cDNA libraries. Nucleic Acids Res. 1988 Jul 11;16(13):6248–6248. doi: 10.1093/nar/16.13.6248. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Refetoff S., DeWind L. T., DeGroot L. J. Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone. J Clin Endocrinol Metab. 1967 Feb;27(2):279–294. doi: 10.1210/jcem-27-2-279. [DOI] [PubMed] [Google Scholar]
  34. Refetoff S., Degroot L. J., Barsano C. P. Defective thyroid hormone feedback regulation in the syndrome of peripheral resistance to thyroid hormone. J Clin Endocrinol Metab. 1980 Jul;51(1):41–45. doi: 10.1210/jcem-51-1-41. [DOI] [PubMed] [Google Scholar]
  35. Refetoff S., Weiss R. E., Usala S. J. The syndromes of resistance to thyroid hormone. Endocr Rev. 1993 Jun;14(3):348–399. doi: 10.1210/edrv-14-3-348. [DOI] [PubMed] [Google Scholar]
  36. Rodriguez-Peña A., Ibarrola N., Iñiguez M. A., Muñoz A., Bernal J. Neonatal hypothyroidism affects the timely expression of myelin-associated glycoprotein in the rat brain. J Clin Invest. 1993 Mar;91(3):812–818. doi: 10.1172/JCI116301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Sakurai A., Miyamoto T., Refetoff S., DeGroot L. J. Dominant negative transcriptional regulation by a mutant thyroid hormone receptor-beta in a family with generalized resistance to thyroid hormone. Mol Endocrinol. 1990 Dec;4(12):1988–1994. doi: 10.1210/mend-4-12-1988. [DOI] [PubMed] [Google Scholar]
  38. Sap J., Muñoz A., Damm K., Goldberg Y., Ghysdael J., Leutz A., Beug H., Vennström B. The c-erb-A protein is a high-affinity receptor for thyroid hormone. Nature. 1986 Dec 18;324(6098):635–640. doi: 10.1038/324635a0. [DOI] [PubMed] [Google Scholar]
  39. Sjöberg M., Vennström B., Forrest D. Thyroid hormone receptors in chick retinal development: differential expression of mRNAs for alpha and N-terminal variant beta receptors. Development. 1992 Jan;114(1):39–47. doi: 10.1242/dev.114.1.39. [DOI] [PubMed] [Google Scholar]
  40. Stewart C. L. Production of chimeras between embryonic stem cells and embryos. Methods Enzymol. 1993;225:823–855. doi: 10.1016/0076-6879(93)25053-5. [DOI] [PubMed] [Google Scholar]
  41. Strait K. A., Schwartz H. L., Perez-Castillo A., Oppenheimer J. H. Relationship of c-erbA mRNA content to tissue triiodothyronine nuclear binding capacity and function in developing and adult rats. J Biol Chem. 1990 Jun 25;265(18):10514–10521. [PubMed] [Google Scholar]
  42. Strait K. A., Zou L., Oppenheimer J. H. Beta 1 isoform-specific regulation of a triiodothyronine-induced gene during cerebellar development. Mol Endocrinol. 1992 Nov;6(11):1874–1880. doi: 10.1210/mend.6.11.1282672. [DOI] [PubMed] [Google Scholar]
  43. Stunnenberg H. G. Mechanisms of transactivation by retinoic acid receptors. Bioessays. 1993 May;15(5):309–315. doi: 10.1002/bies.950150504. [DOI] [PubMed] [Google Scholar]
  44. Takeda K., Sakurai A., DeGroot L. J., Refetoff S. Recessive inheritance of thyroid hormone resistance caused by complete deletion of the protein-coding region of the thyroid hormone receptor-beta gene. J Clin Endocrinol Metab. 1992 Jan;74(1):49–55. doi: 10.1210/jcem.74.1.1727829. [DOI] [PubMed] [Google Scholar]
  45. Tata J. R. Gene expression during metamorphosis: an ideal model for post-embryonic development. Bioessays. 1993 Apr;15(4):239–248. doi: 10.1002/bies.950150404. [DOI] [PubMed] [Google Scholar]
  46. Usala S. J., Bale A. E., Gesundheit N., Weinberger C., Lash R. W., Wondisford F. E., McBride O. W., Weintraub B. D. Tight linkage between the syndrome of generalized thyroid hormone resistance and the human c-erbA beta gene. Mol Endocrinol. 1988 Dec;2(12):1217–1220. doi: 10.1210/mend-2-12-1217. [DOI] [PubMed] [Google Scholar]
  47. Walters S. N., Morell P. Effects of altered thyroid states on myelinogenesis. J Neurochem. 1981 May;36(5):1792–1801. doi: 10.1111/j.1471-4159.1981.tb00433.x. [DOI] [PubMed] [Google Scholar]
  48. Ways D. K., Qin W., Cook P., Parker P. J., Menke J. B., Hao E., Smith A. M., Jones C., Hershman J. M., Geffner M. E. Dominant and nondominant negative C-erbA beta 1 receptors associated with thyroid hormone resistance syndromes augment 12-O-tetradecanoyl-phorbol-13-acetate induction of the collagenase promoter and exhibit defective 3,5,3'-triiodothyronine-mediated repression. Mol Endocrinol. 1993 Sep;7(9):1112–1120. doi: 10.1210/mend.7.9.8247013. [DOI] [PubMed] [Google Scholar]
  49. Weinberger C., Thompson C. C., Ong E. S., Lebo R., Gruol D. J., Evans R. M. The c-erb-A gene encodes a thyroid hormone receptor. Nature. 1986 Dec 18;324(6098):641–646. doi: 10.1038/324641a0. [DOI] [PubMed] [Google Scholar]
  50. Weiss R. E., Stein M. A., Duck S. C., Chyna B., Phillips W., O'Brien T., Gutermuth L., Refetoff S. Low intelligence but not attention deficit hyperactivity disorder is associated with resistance to thyroid hormone caused by mutation R316H in the thyroid hormone receptor beta gene. J Clin Endocrinol Metab. 1994 Jun;78(6):1525–1528. doi: 10.1210/jcem.78.6.8200958. [DOI] [PubMed] [Google Scholar]
  51. Wood W. M., Kao M. Y., Gordon D. F., Ridgway E. C. Thyroid hormone regulates the mouse thyrotropin beta-subunit gene promoter in transfected primary thyrotropes. J Biol Chem. 1989 Sep 5;264(25):14840–14847. [PubMed] [Google Scholar]
  52. Wood W. M., Ocran K. W., Gordon D. F., Ridgway E. C. Isolation and characterization of mouse complementary DNAs encoding alpha and beta thyroid hormone receptors from thyrotrope cells: the mouse pituitary-specific beta 2 isoform differs at the amino terminus from the corresponding species from rat pituitary tumor cells. Mol Endocrinol. 1991 Aug;5(8):1049–1061. doi: 10.1210/mend-5-8-1049. [DOI] [PubMed] [Google Scholar]

Articles from The EMBO Journal are provided here courtesy of Nature Publishing Group

RESOURCES