The N‐terminal part of TIF1, a putative mediator of the ligand‐dependent activation function (AF‐2) of nuclear receptors, is fused to B‐raf in the oncogenic protein T18.

Nuclear receptors (NRs) bound to response elements mediate the effects of cognate ligands on gene expression. Their ligand‐dependent activation function, AF‐2, presumably acts on the basal transcription machinery through intermediary proteins/mediators. We have isolated a mouse nuclear protein, TIF1, which enhances RXR and RAR AF‐2 in yeast and interacts in a ligand‐dependent manner with several NRs in yeast and mammalian cells, as well as in vitro. Remarkably, these interactions require the amino acids constituting the AF‐2 activating domain conserved in all active NRs. Moreover, the oestrogen receptor (ER) AF‐2 antagonist hydroxytamoxifen cannot promote ER‐TIF1 interaction. We propose that TIF1, which contains several conserved domains found in transcriptional regulatory proteins, is a mediator of ligand‐dependent AF‐2. Interestingly, the TIF1 N‐terminal moiety is fused to B‐raf in the mouse oncoprotein T18.

[1]  P. Chambon,et al.  A new version of the two-hybrid assay for detection of protein-protein interactions. , 1995, Nucleic acids research.

[2]  P. Chambon,et al.  Detection of retinoid X receptors using specific monoclonal and polyclonal antibodies. , 1994, Biochemical and biophysical research communications.

[3]  P. Chambon,et al.  Pure and functionally homogeneous recombinant retinoid X receptor. , 1994, The Journal of biological chemistry.

[4]  M. Parker,et al.  Interaction of proteins with transcriptionally active estrogen receptors. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Michael R. Green,et al.  Facilitated binding of TATA-binding protein to nucleosomal DNA , 1994, Nature.

[6]  H. Richard-Foy A way into the packaging , 1994, Nature.

[7]  S. Fields,et al.  The two-hybrid system: an assay for protein-protein interactions. , 1994, Trends in genetics : TIG.

[8]  U. Rapp,et al.  The Raf-1 serine/threonine protein kinase. , 1994, Seminars in cancer biology.

[9]  Michael R. Green,et al.  Nuclear protein CBP is a coactivator for the transcription factor CREB , 1994, Nature.

[10]  A. Nordheim CREB takes CBP to tango , 1994, Nature.

[11]  D. Barettino,et al.  Characterization of the ligand‐dependent transactivation domain of thyroid hormone receptor. , 1994, The EMBO journal.

[12]  W. Sellers,et al.  E1A-associated p300 and CREB-associated CBP belong to a conserved family of coactivators , 1994, Cell.

[13]  G. Martin,et al.  Estrogen receptor-associated proteins: possible mediators of hormone-induced transcription. , 1994, Science.

[14]  M. Carlson,et al.  The SNF/SWI family of global transcriptional activators. , 1994, Current opinion in cell biology.

[15]  H. Chiba,et al.  Two human homologues of Saccharomyces cerevisiae SWI2/SNF2 and Drosophila brahma are transcriptional coactivators cooperating with the estrogen receptor and the retinoic acid receptor. , 1994, Nucleic acids research.

[16]  M. Leid Ligand-induced alteration of the protease sensitivity of retinoid X receptor alpha. , 1994, The Journal of biological chemistry.

[17]  P. Freemont,et al.  The p53-associated protein MDM2 contains a newly characterized zinc-binding domain called the RING finger. , 1994, Trends in biochemical sciences.

[18]  Tom Maniatis,et al.  Transcriptional activation: A complex puzzle with few easy pieces , 1994, Cell.

[19]  P Chambon,et al.  The retinoid signaling pathway: molecular and genetic analyses. , 1994, Seminars in cell biology.

[20]  P. Chambon,et al.  Homo- and heterodimers of the retinoid X receptor (RXR) activated transcription in yeast. , 1994, Nucleic acids research.

[21]  N. Stuurman,et al.  The t(15;17) translocation alters a nuclear body in a retinoic acid‐reversible fashion. , 1994, The EMBO journal.

[22]  P. Chambon,et al.  Dimerization interfaces formed between the DNA binding domains determine the cooperative binding of RXR/RAR and RXR/TR heterodimers to DR5 and DR4 elements. , 1994, The EMBO journal.

[23]  R. Evans,et al.  A novel macromolecular structure is a target of the promyelocyte-retinoic acid receptor oncoprotein , 1994, Cell.

[24]  Maria Carmo-Fonseca,et al.  Retinoic acid regulates aberrant nuclear localization of PML-RARα in acute promyelocytic leukemia cells , 1994, Cell.

[25]  P. Lemotte,et al.  Different agonist- and antagonist-induced conformational changes in retinoic acid receptors analyzed by protease mapping , 1994, Molecular and Cellular Biology.

[26]  P. Chambon,et al.  Role of nuclear retinoic acid receptors in the regulation of gene expression. , 1994 .

[27]  S. Pemrick,et al.  The retinoid receptors. , 1994, Leukemia.

[28]  Y. Ouchi,et al.  Genomic binding-site cloning reveals an estrogen-responsive gene that encodes a RING finger protein. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[29]  Paul A. Khavari,et al.  BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription , 1993, Nature.

[30]  M. Yaniv,et al.  A human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor. , 1993, The EMBO journal.

[31]  Masatoshi Hagiwara,et al.  Phosphorylated CREB binds specifically to the nuclear protein CBP , 1993, Nature.

[32]  P. Chambon,et al.  PMLRAR homodimers: distinct DNA binding properties and heteromeric interactions with RXR. , 1993, The EMBO journal.

[33]  D. Metzger,et al.  Production and characterization of monoclonal antibodies recognising defined regions of the human oestrogen receptor. , 1993, Hybridoma.

[34]  Jonathan A. Cooper,et al.  Mammalian Ras interacts directly with the serine/threonine kinase raf , 1993, Cell.

[35]  D. Reinberg,et al.  Multiple functional domains of human transcription factor IIB: distinct interactions with two general transcription factors and RNA polymerase II. , 1993, Genes & development.

[36]  P. Chambon,et al.  Efficient transactivation by retinoic acid receptors in yeast requires retinoid X receptors. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[37]  M. Carlson,et al.  The yeast SNF2/SWI2 protein has DNA-stimulated ATPase activity required for transcriptional activation. , 1993, Genes & development.

[38]  M. Horikoshi,et al.  The p250 subunit of native TATA box-binding factor TFIID is the cell-cycle regulatory protein CCG1 , 1993, Nature.

[39]  J. Y. Chen,et al.  Multiple parameters control the selectivity of nuclear receptors for their response elements. Selectivity and promiscuity in response element recognition by retinoic acid receptors and retinoid X receptors. , 1993, The Journal of biological chemistry.

[40]  J. Gall,et al.  A putative zinc‐binding protein on lampbrush chromosome loops. , 1993, The EMBO journal.

[41]  P. Freemont The RING finger. A novel protein sequence motif related to the zinc finger. , 1993, Annals of the New York Academy of Sciences.

[42]  G. Thireos,et al.  Two distinct yeast transcriptional activators require the function of the GCN5 protein to promote normal levels of transcription. , 1992, The EMBO journal.

[43]  T. Ishigaki,et al.  RFP is a DNA binding protein associated with the nuclear matrix. , 1992, Nucleic acids research.

[44]  P. Chambon,et al.  Cooperation of proto‐signals for nuclear accumulation of estrogen and progesterone receptors. , 1992, The EMBO journal.

[45]  R. Losson,et al.  Functional analysis of the human estrogen receptor using a phenotypic transactivation assay in yeast. , 1992, Gene.

[46]  P. Chambon,et al.  Multiplicity generates diversity in the retinoic acid signalling pathways. , 1992, Trends in biochemical sciences.

[47]  P. Chambon,et al.  Promoter context- and response element-dependent specificity of the transcriptional activation and modulating functions of retinoic acid receptors , 1992, Cell.

[48]  P. Freemont,et al.  A novel zinc finger coiled-coil domain in a family of nuclear proteins. , 1992, Trends in biochemical sciences.

[49]  P. Chambon,et al.  Immunodetection of multiple species of retinoic acid receptor α : evidence for phosphorylation , 1992 .

[50]  P. Chambon,et al.  Promoter specificity of the two transcriptional activation functions of the human oestrogen receptor in yeast. , 1992, Nucleic acids research.

[51]  P. Chambon,et al.  The acidic transcriptional activator GAL‐VP16 acts on preformed template‐committed complexes. , 1992, The EMBO journal.

[52]  I B Dawid,et al.  The bromodomain: a conserved sequence found in human, Drosophila and yeast proteins. , 1992, Nucleic acids research.

[53]  J. Lees,et al.  Identification of a conserved region required for hormone dependent transcriptional activation by steroid hormone receptors. , 1992, The EMBO journal.

[54]  V. Laudet,et al.  Evolution of the nuclear receptor gene superfamily. , 1992, The EMBO journal.

[55]  Thomas C. Kaufman,et al.  brahma: A regulator of Drosophila homeotic genes structurally related to the yeast transcriptional activator SNF2 SWI2 , 1992, Cell.

[56]  P. Chambon,et al.  Structure, localization and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute promyelocytic leukemia (APL): structural similarities with a new family of oncoproteins. , 1992, The EMBO journal.

[57]  P. Chambon,et al.  Immunodetection of multiple species of retinoic acid receptor alpha: evidence for phosphorylation. , 1992, Experimental cell research.

[58]  T. Fleming,et al.  Development of a highly efficient expression cDNA cloning system: application to oncogene isolation. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[59]  E. Besa Acute promyelocytic leukemia. , 1991, Blood.

[60]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[61]  Elisabeth Scheer,et al.  Distinct classes of transcriptional activating domains function by different mechanisms , 1990, Cell.

[62]  P. Chambon,et al.  Role of the two activating domains of the oestrogen receptor in the cell‐type and promoter‐context dependent agonistic activity of the anti‐oestrogen 4‐hydroxytamoxifen. , 1990, The EMBO journal.

[63]  H. Samuels,et al.  Interactions among a subfamily of nuclear hormone receptors: the regulatory zipper model. , 1990, Molecular endocrinology.

[64]  N. Webster,et al.  The human estrogen receptor has two independent nonacidic transcriptional activation functions , 1989, Cell.

[65]  P. Chambon,et al.  Steroid hormone receptors compete for factors that mediate their enhancer function , 1989, Cell.

[66]  P. Chambon,et al.  The contribution of the N- and C-terminal regions of steroid receptors to activation of transcription is both receptor and cell-specific. , 1989, Nucleic acids research.

[67]  P. Chambon,et al.  Nuclear receptors enhance our understanding of transcription regulation. , 1988, Trends in genetics : TIG.

[68]  P. Chambon,et al.  The human oestrogen receptor functions in yeast , 1988, Nature.

[69]  H. Hiai,et al.  Developmentally regulated expression of a human "finger"-containing gene encoded by the 5' half of the ret transforming gene , 1988, Molecular and cellular biology.

[70]  S. Green,et al.  A versatile in vivo and in vitro eukaryotic expression vector for protein engineering , 1988, Nucleic Acids Res..

[71]  P. Chambon,et al.  Functional domains of the human estrogen receptor , 1987, Cell.