Literature DB >> 8395010

The conserved ninth C-terminal heptad in thyroid hormone and retinoic acid receptors mediates diverse responses by affecting heterodimer but not homodimer formation.

M Au-Fliegner1, E Helmer, J Casanova, B M Raaka, H H Samuels.   

Abstract

The receptors for thyroid hormone (T3R), all-trans-retinoic acid (RAR), and 9-cis-retinoic acid (RXR) bind DNA response elements as homo- and heterodimers. The ligand-binding domains of these receptors contain nine conserved heptads proposed to play a role in dimerization. Mutant receptors with changes in the first or last hydrophobic amino acids in the highly conserved ninth heptad of chick T3R alpha [cT3R alpha(L365R) and cT3R(L372R)] and human RAR alpha (hRAR alpha) [hRAR(M377R) and hRAR(L384R)] reveal that this heptad is essential for certain heterodimeric interactions and for diverse functional activities. Without ligands, wild-type receptors form both homodimers and heterodimers, while these mutants form only homodimers. Surprisingly, the cognate ligand for each mutant enables heterodimer formation between cT3R(L365R) and RAR or RXR and between hRAR(M377R) and T3R or RXR. Both cT3R(L365R) and hRAR(M377R) mediate ligand-dependent transcriptional regulation. However, unlike the wild-type receptor, non-ligand-associated cT3R(L365R) does not suppress the basal activity of certain promoters containing thyroid hormone response elements, suggesting that this silencing effect of T3R is mediated by unliganded heterodimers of T3R and endogenous RXR or related factors. Heterodimerization is also necessary for the strong ligand-independent inhibition between T3R and RAR on a common response element, since the ninth-heptad mutants function as poor inhibitors. However, with a T3R-specific response element, hRAR(M377R) acts as a retinoic acid-dependent inhibitor of cT3R, indicating the importance of heterodimerization for this inhibition. Our studies also suggest that the ninth heptad is necessary for the dominant inhibition of wild-type T3Rs by mutant T3Rs, as has been found for the thyroid hormone-resistant syndrome in humans. Thus, the ninth heptad repeat is required for heterodimerization, suppression of basal promoter activity, and dominant negative effects of T3R and RAR. Lastly, the finding that cT3R(L365R) and hRAR(M377R) require ligands for heterodimer formation also raises the possibility that heterodimeric interactions are mediated by the ninth heptad without ligands but by a second region of these receptors with ligands.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8395010      PMCID: PMC360309          DOI: 10.1128/mcb.13.9.5725-5737.1993

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  65 in total

1.  CAT constructions with multiple unique restriction sites for the functional analysis of eukaryotic promoters and regulatory elements.

Authors:  B Luckow; G Schütz
Journal:  Nucleic Acids Res       Date:  1987-07-10       Impact factor: 16.971

2.  RXR beta: a coregulator that enhances binding of retinoic acid, thyroid hormone, and vitamin D receptors to their cognate response elements.

Authors:  V C Yu; C Delsert; B Andersen; J M Holloway; O V Devary; A M Näär; S Y Kim; J M Boutin; C K Glass; M G Rosenfeld
Journal:  Cell       Date:  1991-12-20       Impact factor: 41.582

3.  Studies of a sibship with apparent hereditary resistance to the intracellular action of thyroid hormone.

Authors:  S Refetoff; L J DeGroot; B Benard; L T DeWind
Journal:  Metabolism       Date:  1972-08       Impact factor: 8.694

4.  The herpes simplex virus thymidine kinase gene promoter contains a novel thyroid hormone response element.

Authors:  H Y Park; D Davidson; B M Raaka; H H Samuels
Journal:  Mol Endocrinol       Date:  1993-03

5.  Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta.

Authors:  A Sakurai; K Takeda; K Ain; P Ceccarelli; A Nakai; S Seino; G I Bell; S Refetoff; L J DeGroot
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

6.  A direct repeat in the cellular retinol-binding protein type II gene confers differential regulation by RXR and RAR.

Authors:  D J Mangelsdorf; K Umesono; S A Kliewer; U Borgmeyer; E S Ong; R M Evans
Journal:  Cell       Date:  1991-08-09       Impact factor: 41.582

7.  A homozygous deletion in the c-erbA beta thyroid hormone receptor gene in a patient with generalized thyroid hormone resistance: isolation and characterization of the mutant receptor.

Authors:  S J Usala; J B Menke; T L Watson; F E Wondisford; B D Weintraub; J Bérard; W E Bradley; S Ono; O T Mueller; B B Bercu
Journal:  Mol Endocrinol       Date:  1991-03

8.  pEXPRESS: a family of expression vectors containing a single transcription unit active in prokaryotes, eukaryotes and in vitro.

Authors:  B M Forman; H H Samuels
Journal:  Gene       Date:  1991-08-30       Impact factor: 3.688

9.  Specificity of a retinoic acid response element in the phosphoenolpyruvate carboxykinase gene promoter: consequences of both retinoic acid and thyroid hormone receptor binding.

Authors:  P C Lucas; B M Forman; H H Samuels; D K Granner
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

10.  Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells.

Authors:  C M Gorman; L F Moffat; B H Howard
Journal:  Mol Cell Biol       Date:  1982-09       Impact factor: 4.272

View more
  33 in total

1.  Multiple mutations contribute to repression by the v-Erb A oncoprotein.

Authors:  Sangho Lee; Martin L Privalsky
Journal:  Oncogene       Date:  2005-10-13       Impact factor: 9.867

2.  Cross-talk between thyroid hormone and specific retinoid X receptor subtypes in yeast selectively regulates cognate ligand actions.

Authors:  P G Walfish; Y F Yang; T Ypganathan; L A Chang; T R Butt
Journal:  Gene Expr       Date:  1996

3.  Regulation of the mdm2 oncogene by thyroid hormone receptor.

Authors:  J S Qi; Y Yuan; V Desai-Yajnik; H H Samuels
Journal:  Mol Cell Biol       Date:  1999-01       Impact factor: 4.272

4.  Transcriptional silencing by unliganded thyroid hormone receptor beta requires a soluble corepressor that interacts with the ligand-binding domain of the receptor.

Authors:  G X Tong; M Jeyakumar; M R Tanen; M K Bagchi
Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

5.  Differential recognition of liganded and unliganded thyroid hormone receptor by retinoid X receptor regulates transcriptional repression.

Authors:  J Zhang; I Zamir; M A Lazar
Journal:  Mol Cell Biol       Date:  1997-12       Impact factor: 4.272

6.  DNA bending by thyroid hormone receptor: influence of half-site spacing and RXR.

Authors:  K Shulemovich; D D Dimaculangan; D Katz; M A Lazar
Journal:  Nucleic Acids Res       Date:  1995-03-11       Impact factor: 16.971

7.  Ligand-dependent occupancy of the retinoic acid receptor beta 2 promoter in vivo.

Authors:  A Dey; S Minucci; K Ozato
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

8.  Expression of human all-trans-retinoic acid receptor beta and its ligand-binding domain in Escherichia coli.

Authors:  M Berggren Söderlund; G Johannesson; G Fex
Journal:  Biochem J       Date:  1995-05-15       Impact factor: 3.857

9.  Mutations that alter ligand-induced switches and dimerization activities in the retinoid X receptor.

Authors:  X K Zhang; G Salbert; M O Lee; M Pfahl
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

10.  Functional evidence for retinoid X receptor (RXR) as a nonsilent partner in the thyroid hormone receptor/RXR heterodimer.

Authors:  Dangsheng Li; Tong Li; Fang Wang; Heather Tian; Herbert H Samuels
Journal:  Mol Cell Biol       Date:  2002-08       Impact factor: 4.272

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.