Chromatin remodeling and control of cell proliferation by progestins via cross talk of progesterone receptor with the estrogen receptors and kinase signaling pathways

Transcription from the mouse mammary tumor virus (MMTV) promoter can be induced by glucocorticoids or progestins. Progesterone treatment of cultured cells carrying an integrated single copy of an MMTV transgene leads to recruitment of progesterone receptor (PR), SWI/SNF, and SNF2h-related complexes...

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Autor principal: Vicent, G.P
Otros Autores: Ballaré, C., Zaurin, R., Saragüeta, P., Beato, M.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Blackwell Publishing Inc. 2006
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a adenosine triphosphate, 15237-44-2, 56-65-5, 987-65-5; lysine, 56-87-1, 6899-06-5, 70-54-2; mitogen activated protein kinase, 142243-02-5; phosphotransferase, 9031-09-8, 9031-44-1; progesterone, 57-83-0; protein kinase B, 148640-14-6; protein tyrosine kinase, 80449-02-1; protein kinase, 9026-43-1; Progestins; Protein Kinases, EC 2.7.1.37; Receptors, Estrogen; Receptors, Progesterone 
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100 1 |a Vicent, G.P. 
245 1 0 |a Chromatin remodeling and control of cell proliferation by progestins via cross talk of progesterone receptor with the estrogen receptors and kinase signaling pathways 
260 |b Blackwell Publishing Inc.  |c 2006 
270 1 0 |m Beato, M.; Center for Genomic Regulation (C.R.G.), PRBB, Dr Aiguader 88, E-08003 Barcelona, Spain; email: miguel.beato@crg.es 
506 |2 openaire  |e Política editorial 
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504 |a HASSAN, A.H., PROCHASSON, P., NEELY, K.E., Function and selectivity of bromodomains in anchoring chromatin-modifying complexes to promoter nucleosomes (2002) Cell, 111, pp. 369-379 
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504 |a O'MALLEY, B.W., CONNEELY, O.M., Orphan receptors: In search of a unifying hypothesis for activation (1992) Mol. Endocrinol, 6, pp. 1359-1361 
504 |a ZARET, K.S., YAMAMOTO, K.R., Reversible and persistent changes in chromatin structure accompany activation of a glucocorticoid-dependent enhancer element (1984) Cell, 38, pp. 29-38 
504 |a CHANDLER, V.L., MALER, B.A., YAMAMOTO, K.R., DNA sequences bound specifically by glucocorticoid receptor in vitro render a heterologous promoter hormone responsive in vivo (1983) Cell, 33, pp. 489-499 
504 |a PAYVAR, F., DEFRANCO, D., FIRESTONE, G.L., Sequence-specific binding of glucocorticoid receptor to MTV DNA at sites within and upstream of the transcribed region (1983) Cell, 35, pp. 381-392 
504 |a SCHEIDEREIT, C., GEISSE, S., WESTPHAL, H.M., BEATO, M., The glucocorticoid receptor binds to defined nucleotide sequences near the promoter of mouse mammary tumour virus (1983) Nature, 304, pp. 749-752 
504 |a CHALEPAKIS, G., ARNEMANN, J., SLATER, E., Differential gene activation by glucocorticoids and progestins through the hormone regulatory element of mouse mammary tumor virus (1988) Cell, 53, pp. 371-382 
504 |a VON DER AHE, D., JANICH, S., SCHEIDEREIT, C., Glucocorticoid and progesterone receptors bind to the same sites in two hormonally regulated promoters (1985) Nature, 313, pp. 706-709 
504 |a CATO, A.C., HENDERSON, D., PONTA, H., The hormone response element of the mouse mammary tumour virus DNA mediates the progestin and androgen induction of transcription in the proviral long terminal repeat region (1987) EMBO J, 6, pp. 363-368 
504 |a RICHARD-FOY, H., HAGER, G.L., Sequence-specific positioning of nucleosomes over the steroid-inducible MMTV promoter (1987) EMBO J, 6, pp. 2321-2328 
504 |a BRUGGEMEIER, U., ROGGE, L., WINNACKER, E.L., BEATO, M., Nuclear factor I acts as a transcription factor on the MMTV promoter but competes with steroid hormone receptors for DNA binding (1990) EMBO J, 9, pp. 2233-2239 
504 |a KALFF, M., GROSS, B., BEATO, M., Progesterone receptor stimulates transcription of mouse mammary tumour virus in a cell-free system (1990) Nature, 344, pp. 360-362 
504 |a TRUSS, M., BARTSCH, J., SCHELBERT, A., Hormone induces binding of receptors and transcription factors to a rearranged nucleosome on the MMTV promoter in vivo (1995) EMBO J, 14, pp. 1737-1751 
504 |a BRÜGGEMEIER, U., KALFF, M., FRANKE, S., Ubiquitous transcription factor OTF-1 mediates induction of the mouse mammary tumour virus promoter through synergistic interaction with hormone receptors (1991) Cell, 64, pp. 565-572 
504 |a PINA, B., BRUGGEMEIER, U., BEATO, M., Nucleosome positioning modulates accessibility of regulatory proteins to the mouse mammary tumor virus promoter (1990) Cell, 60, pp. 719-731 
504 |a EISFELD, K., CANDAU, R., TRUSS, M., BEATO, M., Binding of NF1 to the MMTV promoter in nucleosomes: Influence of rotational phasing, translational positioning and histone H1 (1997) Nucleic Acids Res, 25, pp. 3733-3742 
504 |a BARTSCH, J., TRUSS, M., BODE, J., BEATO, M., Moderate increase in histone acetylation activates the mouse mammary tumor virus promoter and remodels its nucleosome structure (1996) Proc. Natl. Acad. Sci. USA, 93, pp. 10741-10746 
504 |a VENDITTI, P., DI CROCE, L., KAUER, M., Assembly of MMTV promoter minichromosomes with positioned nucleosomes precludes NF1 access but not restriction enzyme cleavage (1998) Nucleic Acids Res, 26, pp. 3657-3666 
504 |a DI CROCE, L., KOOP, R., VENDITTI, P., Two-step synergism between the progesterone receptor and the DNA-binding domain of nuclear factor 1 on MMTV minichromosomes (1999) Mol. Cell, 4, pp. 45-54 
504 |a TSUKIYAMA, T., WU, C., Purification and properties of an ATP-dependent nucleosome remodeling factor (1995) Cell, 83, pp. 1011-1020 
504 |a VICENT, G.P., NACHT, A.S., SMITH, C.L., DNA instructed displacement of histones H2A and H2B at an inducible promoter (2004) Mol. Cell, 16, pp. 439-452 
504 |a SPANGENBERG, C., EISFELD, K., STUNKEL, W., The mouse mammary tumour virus promoter positioned on a tetramer of histones H3 and H4 binds nuclear factor 1 and OTF1 (1998) J. Mol. Biol, 278, pp. 725-739 
504 |a HORN, P.J., CARRUTHERS, L.M., LOGIE, C., Phosphorylation of linker histones regulates ATP-dependent chromatin remodeling enzymes (2002) Nat. Struct. Biol, 9, pp. 263-267 
504 |a VICENT, G.P., MELIA, M.J., BEATO, M., Asymmetric binding of histone H1 stabilizes MMTV nucleosomes and the interaction of progesterone receptor with the exposed HRE (2002) J. Mol. Biol, 324, pp. 501-517 
504 |a KOOP, R., DI CROCE, L., BEATO, M., Histone H1 enhances synergistic activation of the MMTV promoter in chromatin (2003) EMBO J, 22, pp. 588-599 
504 |a BJORNSTROM, L., SJOBERG, M., Mechanisms of estrogen receptor signaling: Convergence of genomic and nongenomic actions on target genes (2005) Mol. Endocrinol, 19, pp. 833-842 
504 |a MIGLIACCIO, A., PICCOLO, D., CASTORIA, G., Activation of the Src/p21ras/Erk pathway by progesterone receptor via cross-talk with estrogen receptor (1998) EMBO J, 17, pp. 2008-2018 
504 |a BALLARE, C., UHRIG, M., BECHTOLD, T., Two domains of the progesterone receptor interact with the estrogen receptor and are required for progesterone activation of the c-Src/Erk pathway in mammalian cells (2003) Mol. Cell. Biol, 23, pp. 1994-2008 
504 |a VICENT, G.P., BALLARE, C., NACHT, A.S., Induction of progesterone target genes requires activation of Erk and Msk kinases and phosphorylation of histone H3 (2006) Mol. Cell, , In press 
504 |a VALLEJO, G., BALLARE, C., BARANAO, J.L., Progestin activation of nongenomic pathways via cross talk of progesterone receptor with estrogen receptor beta induces proliferation of endometrial stromal cells (2005) Mol. Endocrinol, 19, pp. 3023-3037 
520 3 |a Transcription from the mouse mammary tumor virus (MMTV) promoter can be induced by glucocorticoids or progestins. Progesterone treatment of cultured cells carrying an integrated single copy of an MMTV transgene leads to recruitment of progesterone receptor (PR), SWI/SNF, and SNF2h-related complexes to MMTV promoter. Recruitment is accompanied by selective displacement of histones H2A and H2B from the nucleosome B. In nucleosomes assembled on promoter sequences, SWI/SNF displaces histones H2A and H2B from MMTV nucleosome B, but not from other MMTV nucleosomes or from an rDNA promoter nucleosome. Thus, the outcome of nucleosome remodeling by purified SWI/SNF depends on the DNA sequence. On the other hand, 5 min after hormone treatment, the cytoplasmic signaling cascade Src/Ras/Erk is activated via an interaction of PR with the estrogen receptor, which activates Src. As a consequence of Erk activation PR is phosphorylated, Msk1 is activated, and a ternary complex PR-Erk-Msk1 is recruited to MMTV nucleosome B. Msk1 phosphorylates H3 at serine 10, which is followed by acetylation at lysine 14, displacement of HP1γ, and recruitment of Brg1, PCAF, and RNA polymerase II. Blocking Erk activation or Msk1 activity prevents induction of the MMTV transgene. Thus, the rapid nongenomic effects of progestins are essential for their transcriptional effects on certain progestin target genes. In rat endometrial stromal cells, picomolar concentrations of progestins trigger the cross talk of PR with ERβ that activates the Erk and Akt kinase pathways leading to cell proliferation in the absence of direct transcriptional effects of the ligand-activated PR. Thus, depending on the cellular context rapid kinase activation and transcriptional effect play different roles in the physiological response to progestins. © 2006 New York Academy of Sciences.  |l eng 
593 |a Centre de Regulació Genòmica (CRG), Universitat Pompeu Fabra (UPF), PRBB, Dr Aiguader 88, 08003 Barcelona, Spain 
593 |a Instituto de Biología Y Medicina Experimental, CONICET, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina 
593 |a Center for Genomic Regulation (C.R.G.), PRBB, Dr Aiguader 88, E-08003 Barcelona, Spain 
690 1 0 |a CHROMATIN 
690 1 0 |a HISTONE H1 
690 1 0 |a KINASES 
690 1 0 |a MOUSE MAMMARY TUMOR VIRUS 
690 1 0 |a PROGESTERONE RECEPTOR 
690 1 0 |a TRANSCRIPTIONAL REGULATION 
690 1 0 |a ADENOSINE TRIPHOSPHATE 
690 1 0 |a CELL NUCLEUS RECEPTOR 
690 1 0 |a DNA DIRECTED RNA POLYMERASE III 
690 1 0 |a ESTROGEN RECEPTOR 
690 1 0 |a GESTAGEN 
690 1 0 |a HETEROCHROMATIN PROTEIN 1 
690 1 0 |a HISTONE ACETYLTRANSFERASE PCAF 
690 1 0 |a HISTONE H2A 
690 1 0 |a HISTONE H2B 
690 1 0 |a HISTONE H3 
690 1 0 |a LYSINE 
690 1 0 |a MITOGEN ACTIVATED PROTEIN KINASE 
690 1 0 |a PHOSPHOTRANSFERASE 
690 1 0 |a PROGESTERONE 
690 1 0 |a PROGESTERONE RECEPTOR 
690 1 0 |a PROTEIN KINASE B 
690 1 0 |a PROTEIN TYROSINE KINASE 
690 1 0 |a RAS PROTEIN 
690 1 0 |a REGULATOR PROTEIN 
690 1 0 |a RIBOSOME DNA 
690 1 0 |a STEROID RECEPTOR 
690 1 0 |a ESTROGEN RECEPTOR 
690 1 0 |a GESTAGEN 
690 1 0 |a PROGESTERONE RECEPTOR 
690 1 0 |a PROTEIN KINASE 
690 1 0 |a BINDING KINETICS 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a CHROMATIN ASSEMBLY AND DISASSEMBLY 
690 1 0 |a CHROMOSOME ANALYSIS 
690 1 0 |a CONCENTRATION (PARAMETERS) 
690 1 0 |a CONFERENCE PAPER 
690 1 0 |a CYTOPLASM 
690 1 0 |a DNA SEQUENCE 
690 1 0 |a ENDOMETRIUM CELL 
690 1 0 |a ENZYME ACTIVATION 
690 1 0 |a ENZYME ACTIVITY 
690 1 0 |a ENZYME PHOSPHORYLATION 
690 1 0 |a GENE SEQUENCE 
690 1 0 |a HORMONAL REGULATION 
690 1 0 |a HUMAN 
690 1 0 |a MINICHROMOSOME 
690 1 0 |a MITOSIS INHIBITION 
690 1 0 |a MOLECULAR INTERACTION 
690 1 0 |a MOUSE MAMMARY TUMOR ONCOVIRUS 
690 1 0 |a NONHUMAN 
690 1 0 |a NUCLEOSOME 
690 1 0 |a OUTCOME ASSESSMENT 
690 1 0 |a PROMOTER REGION 
690 1 0 |a PROTEIN PROTEIN INTERACTION 
690 1 0 |a PROTEIN PURIFICATION 
690 1 0 |a SIGNAL TRANSDUCTION 
690 1 0 |a TRANSCRIPTION REGULATION 
690 1 0 |a TRANSGENE 
690 1 0 |a ANIMAL 
690 1 0 |a DRUG EFFECT 
690 1 0 |a GENE EXPRESSION REGULATION 
690 1 0 |a GENETICS 
690 1 0 |a METABOLISM 
690 1 0 |a MOUSE 
690 1 0 |a MOUSE MAMMARY TUMOR ONCOVIRUS 
690 1 0 |a RAT 
690 1 0 |a REVIEW 
690 1 0 |a MOUSE MAMMARY TUMOR VIRUS 
690 1 0 |a RATTUS 
690 1 0 |a ANIMALS 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a CHROMATIN ASSEMBLY AND DISASSEMBLY 
690 1 0 |a GENE EXPRESSION REGULATION 
690 1 0 |a MAMMARY TUMOR VIRUS, MOUSE 
690 1 0 |a MICE 
690 1 0 |a PROGESTINS 
690 1 0 |a PROMOTER REGIONS (GENETICS) 
690 1 0 |a PROTEIN KINASES 
690 1 0 |a RATS 
690 1 0 |a RECEPTORS, ESTROGEN 
690 1 0 |a RECEPTORS, PROGESTERONE 
690 1 0 |a SIGNAL TRANSDUCTION 
700 1 |a Ballaré, C. 
700 1 |a Zaurin, R. 
700 1 |a Saragüeta, P. 
700 1 |a Beato, M. 
773 0 |d Blackwell Publishing Inc., 2006  |g v. 1089  |h pp. 59-72  |p Ann. New York Acad. Sci.  |x 00778923  |w (AR-BaUEN)CENRE-1541  |z 1573316695  |z 9781573316699  |t Annals of the New York Academy of Sciences 
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