CBP/p300 in cell growth, transformation, and development.

CREB binding protein (CBP) and p300 were both identified initially in protein interaction assays–the former through its association with the transcription factor CREB (Chrivia et al. 1993) and the latter through its interaction with the adenoviral-transforming protein E1A (Stein et al. 1990; Eckner et al. 1994). The recognition that these two proteins, one involved in transcription and the other in cell transformation, had highly conserved sequences suggested that they had the potential to participate in a variety of cellular functions (Fig. 1). Several excellent reviews (Janknecht and Hunter 1996; Shikama et al. 1997; Giles et al. 1998) have addressed the transcriptional coactivator functions of CBP/p300; this review focuses on the involvement of these proteins in the complex biological processes that affect cell growth, transformation, and development.

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

[2]  A. Baldwin,et al.  THE NF-κB AND IκB PROTEINS: New Discoveries and Insights , 1996 .

[3]  Philip A Beachy,et al.  Hedgehog-Regulated Processing of Gli3 Produces an Anterior/Posterior Repressor Gradient in the Developing Vertebrate Limb , 2000, Cell.

[4]  L. Biesecker,et al.  GLI3 mutations in human disorders mimic Drosophila cubitus interruptus protein functions and localization. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[5]  T. Hunter,et al.  A growing coactivator network , 1996, Nature.

[6]  G. Muscat,et al.  Exogenous expression of a dominant negative RORα1 vector in muscle cells impairs differentiation: RORα1 directly interacts with p300 and MyoD , 1999 .

[7]  P. Becker,et al.  Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila. , 2000, Molecular cell.

[8]  P. Ingham,et al.  Transcriptional activation of hedgehog target genes in Drosophila is mediated directly by the cubitus interruptus protein, a member of the GLI family of zinc finger DNA-binding proteins. , 1996, Genes & development.

[9]  H. Bading,et al.  Control of Recruitment and Transcription-Activating Function of CBP Determines Gene Regulation by NMDA Receptors and L-Type Calcium Channels , 1999, Neuron.

[10]  P. Bénit,et al.  Mutations of the TWIST gene in the Saethre-Chotzene syndrome , 1997, Nature Genetics.

[11]  C. Allis,et al.  ESA1 is a histone acetyltransferase that is essential for growth in yeast. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[12]  J. Pipas,et al.  The amino-terminal functions of the simian virus 40 large T antigen are required to overcome wild-type p53-mediated growth arrest of cells , 1994, Journal of virology.

[13]  A. Wolffe,et al.  p300 stimulates transcription instigated by ligand‐bound thyroid hormone receptor at a step subsequent to chromatin disruption , 1999, The EMBO journal.

[14]  D. Olson,et al.  Thyroid function in Rubinstein-Taybi syndrome. , 1997, The Journal of clinical endocrinology and metabolism.

[15]  H. Ruffner,et al.  CBP/p300 interact with and function as transcriptional coactivators of BRCA1. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[16]  R. D. Hanson,et al.  MLL, a mammalian trithorax-group gene, functions as a transcriptional maintenance factor in morphogenesis. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Q. T. Wang,et al.  Drosophila cubitus interruptus forms a negative feedback loop with patched and regulates expression of Hedgehog target genes. , 1997, Development.

[18]  R. W. Miller,et al.  Tumors in Rubinstein-Taybi syndrome. , 1995, American journal of medical genetics.

[19]  Carlos Caldas,et al.  Mutations truncating the EP300 acetylase in human cancers , 2000, Nature Genetics.

[20]  L. Kedes,et al.  Molecular mechanisms of myogenic coactivation by p300: direct interaction with the activation domain of MyoD and with the MADS box of MEF2C , 1997, Molecular and cellular biology.

[21]  S. Orkin,et al.  A lineage‐selective knockout establishes the critical role of transcription factor GATA‐1 in megakaryocyte growth and platelet development , 1997, The EMBO journal.

[22]  M. Gerritsen,et al.  CREB-binding protein/p300 are transcriptional coactivators of p65. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Interaction and functional collaboration of p300 and C/EBPbeta. , 1997, Molecular and cellular biology.

[24]  J. Chrivia,et al.  CREB-binding Protein Activates Transcription through Multiple Domains* , 1996, The Journal of Biological Chemistry.

[25]  D. Livingston,et al.  p300/MDM2 complexes participate in MDM2-mediated p53 degradation. , 1998, Molecular cell.

[26]  C. Goodman,et al.  A Genetic Analysis of Synaptic Development Pre- and Postsynaptic dCBP Control Transmitter Release at the Drosophila NMJ , 2000, Neuron.

[27]  Zhi-Min Yuan,et al.  Role for p300 in Stabilization of p53 in the Response to DNA Damage* , 1999, The Journal of Biological Chemistry.

[28]  J. Massagué,et al.  Physical and Functional Interaction of SMADs and p300/CBP* , 1998, The Journal of Biological Chemistry.

[29]  M. O’Connor,et al.  The Human Papillomavirus Type 16 E6 Oncoprotein Can Down-Regulate p53 Activity by Targeting the Transcriptional Coactivator CBP/p300 , 1999, Journal of Virology.

[30]  M. Cleary,et al.  CREB Binding Protein Interacts with Nucleoporin-Specific FG Repeats That Activate Transcription and Mediate NUP98-HOXA9 Oncogenicity , 1999, Molecular and Cellular Biology.

[31]  K. Sakaguchi,et al.  DNA damage activates p53 through a phosphorylation-acetylation cascade. , 1998, Genes & development.

[32]  Frank McCormick,et al.  β-Catenin regulates expression of cyclin D1 in colon carcinoma cells , 1999, Nature.

[33]  D. Livingston,et al.  Association of p300 and CBP with simian virus 40 large T antigen , 1996, Molecular and cellular biology.

[34]  H. Giebler,et al.  Human T-Cell Leukemia Virus Type 1 Tax Requires Direct Access to DNA for Recruitment of CREB Binding Protein to the Viral Promoter , 1998, Molecular and Cellular Biology.

[35]  G. Nabel,et al.  Specificity of Cyclin E-Cdk2, TFIIB, and E1A Interactions with a Common Domain of the p300 Coactivator , 1999, Molecular and Cellular Biology.

[36]  L. Kedes,et al.  Regulation of Histone Acetyltransferases p300 and PCAF by the bHLH Protein Twist and Adenoviral Oncoprotein E1A , 1999, Cell.

[37]  S. Ishii,et al.  CBP as a transcriptional coactivator of c-Myb. , 1996, Genes & development.

[38]  Raoul C. M. Hennekam,et al.  Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP , 1995, Nature.

[39]  V. Ogryzko,et al.  Regulation of activity of the transcription factor GATA-1 by acetylation , 1998, Nature.

[40]  J. T. Kadonaga,et al.  Biochemical Analysis of Distinct Activation Functions in p300 That Enhance Transcription Initiation with Chromatin Templates , 1999, Molecular and Cellular Biology.

[41]  G. Lozano,et al.  MDM2 function. , 1998, Biochimica et biophysica acta.

[42]  M. Rivera,et al.  A Role for CREB Binding Protein and p300 Transcriptional Coactivators in Ets-1 Transactivation Functions , 1998, Molecular and Cellular Biology.

[43]  R. Goodman,et al.  Cubitus interruptus Requires DrosophilaCREB-Binding Protein To Activate wingless Expression in theDrosophila Embryo , 2000, Molecular and Cellular Biology.

[44]  B. Howard,et al.  The SV40 large T antigen and adenovirus E1a oncoproteins interact with distinct isoforms of the transcriptional co‐activator, p300. , 1996, The EMBO journal.

[45]  R. Young,et al.  BRCA1 is a component of the RNA polymerase II holoenzyme. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[46]  Randall T. Moon,et al.  The transcriptional coactivator CBP interacts with beta-catenin to activate gene expression. , 2000, The Journal of cell biology.

[47]  R. Hennekam,et al.  Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations , 2000, Journal of medical genetics.

[48]  S. Kidd Characterization of the Drosophila cactus locus and analysis of interactions between cactus and dorsal proteins , 1992, Cell.

[49]  E. Moran DNA tumor virus transforming proteins and the cell cycle. , 1993, Current opinion in genetics & development.

[50]  T. Ouchi,et al.  BRCA1 regulates p53-dependent gene expression. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[51]  Wei Gu,et al.  Synergistic activation of transcription by CBP and p53 , 1997, Nature.

[52]  A. Sundqvist,et al.  The carboxy‐terminal region of adenovirus E1A activates transcription through targeting of a C‐terminal binding protein‐histone deacetylase complex , 1998, FEBS letters.

[53]  Bruce Stillman,et al.  Nucleosomal DNA regulates the core-histone-binding subunit of the human Hat1 acetyltransferase , 1998, Current Biology.

[54]  J. Nyborg,et al.  The Human T-Cell Leukemia Virus Type 1 Oncoprotein Tax Inhibits the Transcriptional Activity of c-Myb through Competition for the CREB Binding Protein , 1998, Journal of Virology.

[55]  T. Braun,et al.  Inhibition of muscle differentiation by the adenovirus E1a protein: repression of the transcriptional activating function of the HLH protein Myf-5. , 1992, Genes & development.

[56]  C. Glass,et al.  Differential use of CREB binding protein-coactivator complexes. , 1998, Science.

[57]  Stephen N. Jones,et al.  Regulation of p53 stability by Mdm2 , 1997, Nature.

[58]  J. Yu,et al.  Three unrelated viral transforming proteins (vIRF, EBNA2, and E1A) induce the MYC oncogene through the interferon-responsive PRF element by using different transcription coadaptors. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[59]  M J May,et al.  NF-kappa B and Rel proteins: evolutionarily conserved mediators of immune responses. , 1998, Annual review of immunology.

[60]  L. Tsai,et al.  Involvement of the cell-cycle inhibitor Cip1/WAF1 and the E1A-associated p300 protein in terminal differentiation. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[61]  G. Muscat,et al.  The orphan nuclear receptor, COUP-TF II, inhibits myogenesis by post-transcriptional regulation of MyoD function: COUP-TF II directly interacts with p300 and myoD. , 1998, Nucleic acids research.

[62]  K. Toth,et al.  Transcription factor TFIID is a direct functional target of the adenovirus E1A transcription-repression domain. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[63]  T. Nabeshima,et al.  Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism. , 1999, Human molecular genetics.

[64]  E. Jabs,et al.  Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations. , 1998, American journal of human genetics.

[65]  F. Kashanchi,et al.  The Coactivator CBP Stimulates Human T-cell Lymphotrophic Virus Type I Tax Transactivation in Vitro * , 1998, The Journal of Biological Chemistry.

[66]  S. Ghosh,et al.  Phosphorylation of NF-kappa B p65 by PKA stimulates transcriptional activity by promoting a novel bivalent interaction with the coactivator CBP/p300. , 1998, Molecular cell.

[67]  T. Unger,et al.  Critical role for Ser20 of human p53 in the negative regulation of p53 by Mdm2 , 1999, The EMBO journal.

[68]  A. Giordano,et al.  p300 is required for MyoD‐dependent cell cycle arrest and muscle‐specific gene transcription , 1997, The EMBO journal.

[69]  P. Simpson,et al.  Maternal-Zygotic Gene Interactions during Formation of the Dorsoventral Pattern in Drosophila Embryos. , 1983, Genetics.

[70]  E. Verdin,et al.  Acetylation of the HIV-1 Tat protein by p300 is important for its transcriptional activity , 1999, Current Biology.

[71]  D. Latchman,et al.  CBP associates with the p42/p44 MAPK enzymes and is phosphorylated following NGF treatment. , 1999, NeuroReport.

[72]  O. Rozenblatt-Rosen,et al.  The C-terminal SET domains of ALL-1 and TRITHORAX interact with the INI1 and SNR1 proteins, components of the SWI/SNF complex. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[73]  J. Manley,et al.  Selective nuclear transport of the Drosophila morphogen dorsal can be established by a signaling pathway involving the transmembrane protein Toll and protein kinase A. , 1992, Genes & development.

[74]  R. Gaynor,et al.  HTLV-1 21 bp repeat sequences facilitate stable association between Tax and CREB to increase CREB binding affinity. , 1996, Journal of molecular biology.

[75]  M. Ohki,et al.  Interaction and functional cooperation of the leukemia‐associated factors AML1 and p300 in myeloid cell differentiation , 1998, The EMBO journal.

[76]  D. Livingston,et al.  Distinct roles of the co-activators p300 and CBP in retinoic-acid-induced F9-cell differentiation , 1998, Nature.

[77]  B. Thisse,et al.  Sequence of the twist gene and nuclear localization of its protein in endomesodermal cells of early Drosophila embryos. , 1988, The EMBO journal.

[78]  A. Nordheim,et al.  MAP kinase-dependent transcriptional coactivation by Elk-1 and its cofactor CBP. , 1996, Biochemical and biophysical research communications.

[79]  A. R. I. Altaba Gli proteins and Hedgehog signaling: development and cancer. , 1999 .

[80]  H. Ugai,et al.  The coactivators p300 and CBP have different functions during the differentiation of F9 cells , 1999, Journal of Molecular Medicine.

[81]  J. M. Boyd,et al.  A region in the C‐terminus of adenovirus 2/5 E1a protein is required for association with a cellular phosphoprotein and important for the negative modulation of T24‐ras mediated transformation, tumorigenesis and metastasis. , 1993, The EMBO journal.

[82]  I. Verma,et al.  Transcriptional activation by BRCA1 , 1996, Nature.

[83]  C. Glass,et al.  Factor-specific modulation of CREB-binding protein acetyltransferase activity. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[84]  E. Kieff,et al.  Epstein – Barr virus nuclear protein 2 interacts with p 300 , CBP , and PCAF histone acetyltransferases in activation of the LMP 1 promoter , 1999 .

[85]  S A Wasserman,et al.  A gradient of cactus protein degradation establishes dorsoventral polarity in the Drosophila embryo. , 1996, Developmental biology.

[86]  Wei Gu,et al.  Activation of p53 Sequence-Specific DNA Binding by Acetylation of the p53 C-Terminal Domain , 1997, Cell.

[87]  Mariann Bienz,et al.  Drosophila CBP represses the transcription factor TCF to antagonize Wingless signalling , 1998, Nature.

[88]  Andrew J. Bannister,et al.  Stimulation of c-Jun activity by CBP: c-Jun residues Ser63/73 are required for CBP induced stimulation in vivo and CBP binding in vitro. , 1995, Oncogene.

[89]  Yasunori Tanaka,et al.  Sonic Hedgehog-induced Activation of the Gli1Promoter Is Mediated by GLI3* , 1999, The Journal of Biological Chemistry.

[90]  N. Shiama The p300/CBP family: integrating signals with transcription factors and chromatin. , 1997, Trends in cell biology.

[91]  Anirvan Ghosh,et al.  Regulation of CBP-Mediated Transcription by Neuronal Calcium Signaling , 1999, Neuron.

[92]  A. Levine,et al.  Nuclear Export Is Required for Degradation of Endogenous p53 by MDM2 and Human Papillomavirus E6 , 1998, Molecular and Cellular Biology.

[93]  K. Webster,et al.  Adenovirus E1A Inhibits Cardiac Myocyte-specific Gene Expression through Its Amino Terminus* , 1997, The Journal of Biological Chemistry.

[94]  R. Behringer,et al.  twist is required in head mesenchyme for cranial neural tube morphogenesis. , 1995, Genes & development.

[95]  H. Masuya,et al.  Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein-Taybi syndrome. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[96]  N. Andrews,et al.  The transcriptional integrator CREB-binding protein mediates positive cross talk between nuclear hormone receptors and the hematopoietic bZip protein p45/NF-E2 , 1997, Molecular and cellular biology.

[97]  A. Joyner,et al.  Gli genes in development and cancer , 1999, Oncogene.

[98]  R. Goodman,et al.  Mutants of cubitus interruptus that are independent of PKA regulation are independent of hedgehog signaling. , 1999, Development.

[99]  Jeffrey D. Parvin,et al.  RNA Helicase A Mediates Association of CBP with RNA Polymerase II , 1997, Cell.

[100]  A. Giordano,et al.  Regulation of MyoD gene transcription and protein function by the transforming domains of the adenovirus E1A oncoprotein. , 1993, Oncogene.

[101]  G. Nabel,et al.  Regulation of NF-κB by Cyclin-Dependent Kinases Associated with the p300 Coactivator , 1997, Science.

[102]  P. Yaciuk,et al.  Analysis of E1A-mediated growth regulation functions: binding of the 300-kilodalton cellular product correlates with E1A enhancer repression function and DNA synthesis-inducing activity , 1990, Journal of virology.

[103]  F. Behm,et al.  All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders. , 1997, Blood.

[104]  Mariann Bienz,et al.  LEF-1, a Nuclear Factor Coordinating Signaling Inputs from wingless and decapentaplegic , 1997, Cell.

[105]  T. Kornberg,et al.  Proteolysis That Is Inhibited by Hedgehog Targets Cubitus interruptus Protein to the Nucleus and Converts It to a Repressor , 1997, Cell.

[106]  M. Horikoshi,et al.  Novel Substrate Specificity of the Histone Acetyltransferase Activity of HIV-1-Tat Interactive Protein Tip60* , 1997, The Journal of Biological Chemistry.

[107]  D. Latchman,et al.  Nerve Growth Factor Up-regulates the Transcriptional Activity of CBP through Activation of the p42/p44MAPK Cascade* , 1998, The Journal of Biological Chemistry.

[108]  D. Patel,et al.  The E6 protein of human papillomavirus type 16 binds to and inhibits co‐activation by CBP and p300 , 1999, The EMBO journal.

[109]  H. Giebler,et al.  Binding of p53 to the KIX Domain of CREB Binding Protein , 1999, The Journal of Biological Chemistry.

[110]  M Oelgeschläger,et al.  Interaction of the co‐activator CBP with Myb proteins: effects on Myb‐specific transactivation and on the cooperativity with NF‐M. , 1996, The EMBO journal.

[111]  N. Perkins,et al.  Transcriptional Cross Talk between NF-κB and p53 , 1999, Molecular and Cellular Biology.

[112]  C. Nüsslein-Volhard,et al.  cactus, a maternal gene required for proper formation of the dorsoventral morphogen gradient in Drosophila embryos. , 1991, Development.

[113]  L. Kedes,et al.  Adenovirus E1A products suppress myogenic differentiation and inhibit transcription from muscle-specific promoters , 1988, Nature.

[114]  E. Zackai,et al.  TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome. , 1999, American journal of medical genetics.

[115]  W. Kaelin,et al.  MDM2 Suppresses p73 Function without Promoting p73 Degradation , 1999, Molecular and Cellular Biology.

[116]  D. Livingston,et al.  Binding and modulation of p53 by p300/CBP coactivators , 1997, Nature.

[117]  E. Lees,et al.  Mammalian Srb/Mediator complex is targeted by adenovirus E1A protein , 1999, Nature.

[118]  S. Orkin,et al.  CREB-binding protein cooperates with transcription factor GATA-1 and is required for erythroid differentiation. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[119]  J. Choe,et al.  cAMP Response Element-binding Protein-binding Protein Binds to Human Papillomavirus E2 Protein and Activates E2-dependent Transcription* , 2000, The Journal of Biological Chemistry.

[120]  P. Wright,et al.  Role of Secondary Structure in Discrimination between Constitutive and Inducible Activators , 1999, Molecular and Cellular Biology.

[121]  D. Trouche,et al.  The CBP co-activator stimulates E2F1/DP1 activity. , 1996, Nucleic acids research.

[122]  Arun J Sharma,et al.  The NeuroD1/BETA2 Sequences Essential for Insulin Gene Transcription Colocalize with Those Necessary for Neurogenesis and p300/CREB Binding Protein Binding , 1999, Molecular and Cellular Biology.

[123]  R. Aguiar,et al.  A Novel Fusion Between MOZand the Nuclear Receptor Coactivator TIF2in Acute Myeloid Leukemia , 1998 .

[124]  C. Glass,et al.  Transcriptional Activation by NF-κB Requires Multiple Coactivators , 1999, Molecular and Cellular Biology.

[125]  R. Brennan,et al.  The Human T-cell Leukemia Virus-1 Transcriptional Activator Tax Enhances cAMP-responsive Element-binding Protein (CREB) Binding Activity through Interactions with the DNA Minor Groove* , 1998, The Journal of Biological Chemistry.

[126]  R. Roeder,et al.  Interaction of the human T-cell lymphotropic virus type 1 tax transactivator with transcription factor IIA , 1996, Molecular and cellular biology.

[127]  W. Gelbart,et al.  A transcript from a Drosophila pattern gene predicts a protein homologous to the transforming growth factor-β family , 1987, Nature.

[128]  R. Wadgaonkar,et al.  Murine Double Minute (MDM2) Blocks p53-coactivator Interaction, a New Mechanism for Inhibition of p53-dependent Gene Expression* , 1999, The Journal of Biological Chemistry.

[129]  A. Joyner,et al.  A mouse model of Greig cephalo–polysyndactyly syndrome: the extra–toesJ mutation contains an intragenic deletion of the Gli3 gene , 1993, Nature Genetics.

[130]  C. Nüsslein-Volhard,et al.  Mutations affecting segment number and polarity in Drosophila , 1980, Nature.

[131]  H. Bading,et al.  CBP: a signal-regulated transcriptional coactivator controlled by nuclear calcium and CaM kinase IV. , 1998, Science.

[132]  K. Gardner,et al.  Recruitment of p300/CBP in p53-Dependent Signal Pathways , 1997, Cell.

[133]  F. Gage,et al.  The Signal-Dependent Coactivator CBP Is a Nuclear Target for pp90RSK , 1996, Cell.

[134]  Y. Shi,et al.  Adenovirus E1A downregulates cJun- and JunB-mediated transcription by targeting their coactivator p300 , 1996, Molecular and cellular biology.

[135]  S. Ishii,et al.  Inhibitory interaction of c-Myb and GATA-1 via transcriptional co-activator CBP , 2000, Oncogene.

[136]  R. Evans,et al.  Localization of nascent RNA and CREB binding protein with the PML-containing nuclear body. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[137]  N. Shikama,et al.  A novel cofactor for p300 that regulates the p53 response. , 1999, Molecular cell.

[138]  R. Weichselbaum,et al.  Function for p300 and not CBP in the apoptotic response to DNA damage , 1999, Oncogene.

[139]  K. Yamamoto,et al.  Adenovirus E1A specifically blocks SWI/SNF-dependent transcriptional activation , 1996, Molecular and cellular biology.

[140]  C. Glass,et al.  Signal-specific co-activator domain requirements for Pit-1 activation , 1998, Nature.

[141]  R. Goodman,et al.  Adenoviral ElA-associated protein p300 as a functional homologue of the transcriptional co-activator CBP , 1995, Nature.

[142]  R. Kitsis,et al.  Transcriptional Coactivator p300 Stimulates Cell Type-specific Gene Expression in Cardiac Myocytes* , 1997, The Journal of Biological Chemistry.

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

[144]  Tony Kouzarides,et al.  Retinoblastoma protein recruits histone deacetylase to repress transcription , 1998, Nature.

[145]  E. Stavridi,et al.  Phosphorylation of Ser-20 mediates stabilization of human p53 in response to DNA damage. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[146]  R. Stein,et al.  p300 functions as a transcriptional coactivator for the TAL1/SCL oncoprotein , 1999, Oncogene.

[147]  S. Ishii,et al.  Drosophila CBP is a co-activator of cubitus interruptus in hedgehog signalling , 1997, Nature.

[148]  F. Kashanchi,et al.  Phosphorylation of p53 Serine 15 Increases Interaction with CBP* , 1998, The Journal of Biological Chemistry.

[149]  H. Shih,et al.  Control of cAMP-regulated enhancers by the viral transactivator Tax through CREB and the co-activator CBP , 1996, Nature.

[150]  R. Gaynor,et al.  Complex formation between CREB and Tax enhances the binding affinity of CREB for the human T-cell leukemia virus type 1 21-base-pair repeats , 1996, Molecular and cellular biology.

[151]  H. Giebler,et al.  Anchoring of CREB binding protein to the human T-cell leukemia virus type 1 promoter: a molecular mechanism of Tax transactivation , 1997, Molecular and cellular biology.

[152]  A. Sparks,et al.  Identification of c-MYC as a target of the APC pathway. , 1998, Science.

[153]  D. Wettstein,et al.  Activation of Xenopus Genes Required for Lateral Inhibition and Neuronal Differentiation during Primary Neurogenesis , 1999, Molecular and Cellular Neuroscience.

[154]  R. Evans,et al.  Modulation of CREB binding protein function by the promyelocytic (PML) oncoprotein suggests a role for nuclear bodies in hormone signaling. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[155]  Michael E. Greenberg,et al.  Coupling of the RAS-MAPK Pathway to Gene Activation by RSK2, a Growth Factor-Regulated CREB Kinase , 1996, Science.

[156]  D. Dean,et al.  Rb Interacts with Histone Deacetylase to Repress Transcription , 1998, Cell.

[157]  R. Derynck,et al.  The tumor suppressor Smad4/DPC4 and transcriptional adaptor CBP/p300 are coactivators for smad3 in TGF-beta-induced transcriptional activation. , 1998, Genes & development.

[158]  L. Cohen,et al.  A novel mechanism for cyclic adenosine 3',5'-monophosphate regulation of gene expression by CREB-binding protein. , 1999, Molecular endocrinology.

[159]  T. Maniatis Catalysis by a Multiprotein IκB Kinase Complex , 1997, Science.

[160]  W. Kraus,et al.  E1A-mediated inhibition of myogenesis correlates with a direct physical interaction of E1A12S and basic helix-loop-helix proteins , 1993, Molecular and cellular biology.

[161]  Tae Hoon Kim,et al.  Efficient recruitment of TFIIB and CBP-RNA polymerase II holoenzyme by an interferon-beta enhanceosome in vitro. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[162]  C. Hui,et al.  Developmentally regulated expression of the transcriptional cofactors/histone acetyltransferases CBP and p300 during mouse embryogenesis. , 1999, The International journal of developmental biology.

[163]  K. Tashiro,et al.  Molecular cloning and expression of Xenopus p300/CBP. , 1998, Biochimica et biophysica acta.

[164]  L. Kedes,et al.  Acetylation of MyoD directed by PCAF is necessary for the execution of the muscle program. , 1999, Molecular cell.

[165]  A. Harel-Bellan,et al.  Phosphorylation by p44 MAP Kinase/ERK1 stimulates CBP histone acetyl transferase activity in vitro. , 1999, Biochemical and biophysical research communications.

[166]  K. Senger,et al.  Acetylation of HMG I(Y) by CBP turns off IFN beta expression by disrupting the enhanceosome. , 1998, Molecular cell.

[167]  M. Tsai,et al.  The basic helix-loop-helix protein BETA2 interacts with p300 to coordinate differentiation of secretin-expressing enteroendocrine cells. , 1998, Genes & development.

[168]  Y. Nakatani,et al.  An Exposed KID-Like Domain in Human T-Cell Lymphotropic Virus Type 1 Tax Is Responsible for the Recruitment of Coactivators CBP/p300 , 1998, Molecular and Cellular Biology.

[169]  L. Kirshenbaum,et al.  Adenovirus E1A Represses Cardiac Gene Transcription and Reactivates DNA Synthesis in Ventricular Myocytes, via Alternative Pocket Protein- and p300-binding Domains (*) , 1995, The Journal of Biological Chemistry.

[170]  S. Ishii,et al.  Drosophila CBP is required for dorsal–dependent twist gene expression , 1997, Nature Genetics.

[171]  G. Condorelli,et al.  Human p300 Protein Is a Coactivator for the Transcription Factor MyoD (*) , 1996, The Journal of Biological Chemistry.

[172]  W. McGinnis,et al.  A genetic screen of the Drosophila X chromosome for mutations that modify Deformed function. , 1998, Genetics.

[173]  H. Esche,et al.  cAMP-independent Activation of the Adenovirus Type 12 E2 Promoter Correlates with the Recruitment of CREB-1/ATF-1, E1A12S, and CBP to the E2-CRE* , 2000, The Journal of Biological Chemistry.

[174]  T. Iwama,et al.  p300 gene alterations in colorectal and gastric carcinomas. , 1996, Oncogene.

[175]  W. Zhang,et al.  Acetylation and modulation of erythroid Krüppel-like factor (EKLF) activity by interaction with histone acetyltransferases. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[176]  M. Oren,et al.  Mdm2 promotes the rapid degradation of p53 , 1997, Nature.

[177]  R. Evans,et al.  A Viral Mechanism for Inhibition of p300 and PCAF Acetyltransferase Activity , 1999, Cell.

[178]  J B Lawrence,et al.  Molecular cloning and functional analysis of the adenovirus E1A-associated 300-kD protein (p300) reveals a protein with properties of a transcriptional adaptor. , 1994, Genes & development.

[179]  T. Kouzarides,et al.  Regulation of E2F1 activity by acetylation , 2000, The EMBO journal.

[180]  E. Green,et al.  Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome , 1997, Nature Genetics.

[181]  E. Kieff,et al.  Epstein-Barr virus nuclear protein 2 interacts with p300, CBP, and PCAF histone acetyltransferases in activation of the LMP1 promoter. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[182]  R. Goodman,et al.  Protein kinase A directly regulates the activity and proteolysis of cubitus interruptus. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[183]  K. Anderson,et al.  Signaling pathways that establish the dorsal-ventral pattern of the Drosophila embryo. , 1995, Annual review of genetics.

[184]  M. Karin,et al.  Activation of cAMP and mitogen responsive genes relies on a common nuclear factor , 1994, Nature.

[185]  A. Zantema,et al.  The adenovirus E1A-associated 300 kDa adaptor protein counteracts the inhibition of the collagenase promoter by E1A and represses transformation. , 1996, Oncogene.

[186]  Jye-Yee Lin,et al.  Functional impairment of p73 and p51, the p53-related proteins, by the human T-cell leukemia virus type 1 Tax oncoprotein , 2000, Oncogene.

[187]  C. Allis,et al.  The language of covalent histone modifications , 2000, Nature.

[188]  T. Suda,et al.  Mice homozygous for a truncated form of CREB-binding protein exhibit defects in hematopoiesis and vasculo-angiogenesis. , 1999, Blood.

[189]  G. Blobel,et al.  CREB-Binding Protein Acetylates Hematopoietic Transcription Factor GATA-1 at Functionally Important Sites , 1999, Molecular and Cellular Biology.

[190]  T. Hunter,et al.  TGF-beta-stimulated cooperation of smad proteins with the coactivators CBP/p300. , 1998, Genes & development.

[191]  Konrad Basler,et al.  Sending and Receiving the Hedgehog Signal: Control by the Drosophila Gli Protein Cubitus interruptus , 1996, Science.

[192]  D. Livingston,et al.  Phosphorylation of the adenovirus E1A‐associated 300 kDa protein in response to retinoic acid and E1A during the differentiation of F9 cells. , 1995, The EMBO journal.

[193]  G. Gillessen‐kaesbach,et al.  Identification of a frameshift mutation in the gene TWISTin a family affected with Robinow-Sorauf syndrome , 1999, Journal of Medical Genetics.

[194]  J H RUBINSTEIN,et al.  Broad thumbs and toes and facial abnormalities. A possible mental retardation syndrome. , 1963, American journal of diseases of children.

[195]  M. Breuning,et al.  Conjunction dysfunction: CBP/p300 in human disease. , 1998, Trends in genetics : TIG.

[196]  Andrew J. Bannister,et al.  CBP‐induced stimulation of c‐Fos activity is abrogated by E1A. , 1995, The EMBO journal.

[197]  D. Housman,et al.  MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3). , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[198]  J. Nevins,et al.  Interaction of the Dr1 inhibitory factor with the TATA binding protein is disrupted by adenovirus E1A. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[199]  A. Wolffe,et al.  Acetylation of general transcription factors by histone acetyltransferases , 1997, Current Biology.

[200]  S. Balcı,et al.  FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy , 1999, European Journal of Human Genetics.

[201]  Takeshi Suzuki,et al.  Tax protein of HTLV-1 inhibits CBP/p300-mediated transcription by interfering with recruitment of CBP/p300 onto DNA element of E-box or p53 binding site , 1999, Oncogene.

[202]  A. Levine,et al.  The p53-mdm-2 autoregulatory feedback loop. , 1993, Genes & development.

[203]  D. Lacombe,et al.  Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndrome. , 1998, American journal of medical genetics.

[204]  A. Wolffe,et al.  Xenopus NF‐Y pre‐sets chromatin to potentiate p300 and acetylation‐responsive transcription from the Xenopus hsp70 promoter in vivo , 1998, The EMBO journal.

[205]  S. Orkin,et al.  Erythroid differentiation in chimaeric mice blocked by a targeted mutation in the gene for transcription factor GATA-1 , 1991, Nature.

[206]  Y. Hayashi,et al.  Adenoviral E1A-associated protein p300 is involved in acute myeloid leukemia with t(11;22)(q23;q13). , 1997, Blood.

[207]  L. Biesecker Strike three for GLI3 , 1997, Nature Genetics.

[208]  C. Nüsslein-Volhard,et al.  cactus, a gene involved in dorsoventral pattern formation of Drosophila, is related to the IκB gene family of vertebrates , 1992, Cell.

[209]  D. Livingston,et al.  A family of transcriptional adaptor proteins targeted by the E1A oncoprotein , 1995, Nature.

[210]  J. Craig,et al.  Recruitment of CREB Binding Protein Is Sufficient for CREB-Mediated Gene Activation , 2000, Molecular and Cellular Biology.

[211]  A. Mal,et al.  The adenovirus E1A 289R and 243R proteins inhibit the phosphorylation of p300. , 1994, Oncogene.

[212]  J. Nyborg,et al.  Binding of the human T-cell leukemia virus Tax protein to the coactivator CBP interferes with CBP-mediated transcriptional control , 1999, Oncogene.

[213]  R. Steward,et al.  The dorsoventral signal transduction pathway and the Rel-like transcription factors in Drosophila. , 1997, Seminars in cancer biology.

[214]  M. Scheffner,et al.  The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53 , 1993, Cell.

[215]  D. Livingston,et al.  Interaction and functional collaboration of p300/CBP and bHLH proteins in muscle and B-cell differentiation. , 1996, Genes & development.

[216]  H. Esche,et al.  Differences in the interactions of oncogenic adenovirus 12 early region 1A and nononcogenic adenovirus 2 early region 1A with the cellular coactivators p300 and CBP. , 1999, Virology.

[217]  Mariann Bienz,et al.  A function of CBP as a transcriptional co‐activator during Dpp signalling , 1999, The EMBO journal.

[218]  J. Girault,et al.  Histone acetyltransferase activity of CBP is controlled by cycle-dependent kinases and oncoprotein E1A , 1998, Nature.

[219]  P. Yaciuk,et al.  Simian virus 40 large-T antigen expresses a biological activity complementary to the p300-associated transforming function of the adenovirus E1A gene products , 1991, Molecular and cellular biology.

[220]  S. Berger,et al.  p53 Sites Acetylated In Vitro by PCAF and p300 Are Acetylated In Vivo in Response to DNA Damage , 1999, Molecular and Cellular Biology.

[221]  C. Mello,et al.  A CBP/p300 homolog specifies multiple differentiation pathways in Caenorhabditis elegans. , 1998, Genes & development.

[222]  M. Nemethova,et al.  Polyomavirus Large T Antigen Binds the Transcriptional Coactivator Protein p300 , 1999, Journal of Virology.

[223]  Y. Shi,et al.  Neuralization of the Xenopus Embryo by Inhibition of p300/ CREB-Binding Protein Function , 1999, The Journal of Neuroscience.

[224]  N. Perkins,et al.  Transcriptional cross talk between NF-kappaB and p53. , 1999, Molecular and cellular biology.

[225]  C. McCallum,et al.  The Drosophila trithorax group proteins BRM, ASH1 and ASH2 are subunits of distinct protein complexes. , 1998, Development.

[226]  C. Disteche,et al.  The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein , 1996, Nature Genetics.

[227]  R. W. Lee,et al.  Ability of adenovirus 5 E1A proteins to suppress differentiation of BC3H1 myoblasts correlates with their binding to a 300 kDa cellular protein. , 1992, Molecular biology of the cell.

[228]  D. Livingston,et al.  Gene dose-dependent control of hematopoiesis and hematologic tumor suppression by CBP. , 2000, Genes & development.

[229]  R. Goodman,et al.  Differential Activation of Viral and Cellular Promoters by Human T-cell Lymphotropic Virus-1 Tax and cAMP-responsive Element Modulator Isoforms* , 1997, The Journal of Biological Chemistry.

[230]  S. Tsuzuki,et al.  c-Myb acetylation at the carboxyl-terminal conserved domain by transcriptional co-activator p300 , 2000, Oncogene.

[231]  Stuart L Schreiber,et al.  Histone Deacetylase Activity Is Required for Full Transcriptional Repression by mSin3A , 1997, Cell.

[232]  G. Blobel CREB-binding protein and p300: molecular integrators of hematopoietic transcription. , 2000, Blood.

[233]  J. Yan,et al.  Molecular interactions between the coactivator CBP and the human T-cell leukemia virus Tax protein. , 1998, Journal of molecular biology.

[234]  L. Kedes,et al.  Differential roles of p300 and PCAF acetyltransferases in muscle differentiation. , 1997, Molecular cell.

[235]  B. Howard,et al.  A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A , 1996, Nature.

[236]  H. Arnold,et al.  A novel E1A domain mediates skeletal-muscle-specific enhancer repression independently of pRB and p300 binding , 1996, Molecular and cellular biology.

[237]  H. Erdjument-Bromage,et al.  The Transcriptional Activity of NF-κB Is Regulated by the IκB-Associated PKAc Subunit through a Cyclic AMP–Independent Mechanism , 1997, Cell.

[238]  L. Pillus,et al.  Yeast SAS silencing genes and human genes associated with AML and HIV–1 Tat interactions are homologous with acetyltransferases , 1996, Nature Genetics.

[239]  M. Braun,et al.  Structural and transcriptional analysis of human papillomavirus type 16 sequences in cervical carcinoma cell lines , 1987, Journal of virology.