Transcriptional Activation by the Ewing's Sarcoma (EWS) Oncogene Can Be Cis-repressed by the EWS RNA-binding Domain*
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[1] M. Green,et al. The HIV-1 Tat protein activates transcription from an upstream DNA-binding site: implications for Tat function. , 1991, Genes & development.
[2] L. Tora,et al. The N-terminal domain of human TAFII68 displays transactivation and oncogenic properties , 1999, Oncogene.
[3] C. Gunter,et al. Purified Recombinant Fmrp Exhibits Selective RNA Binding as an Intrinsic Property of the Fragile X Mental Retardation Protein* , 1998, The Journal of Biological Chemistry.
[4] C. Burd,et al. Conserved structures and diversity of functions of RNA-binding proteins. , 1994, Science.
[5] S. Pan,et al. The EWS/ATF1 fusion protein contains a dispersed activation domain that functions directly , 1998, Oncogene.
[6] L. Lee,et al. The EWS-ATF-1 gene involved in malignant melanoma of soft parts with t(12;22) chromosome translocation, encodes a constitutive transcriptional activator. , 1996, Oncogene.
[7] D. Immanuel,et al. TLS (FUS) binds RNA in vivo and engages in nucleo-cytoplasmic shuttling. , 1997, Journal of cell science.
[8] Olivier Delattre,et al. EWS, but Not EWS-FLI-1, Is Associated with Both TFIID and RNA Polymerase II: Interactions between Two Members of the TET Family, EWS and hTAFII68, and Subunits of TFIID and RNA Polymerase II Complexes , 1998, Molecular and Cellular Biology.
[9] H. Zinszner,et al. A novel effector domain from the RNA-binding protein TLS or EWS is required for oncogenic transformation by CHOP. , 1994, Genes & development.
[10] K. A. Lee,et al. In vitro phosphorylation studies of a conserved region of the transcription factor ATF1. , 1993, Nucleic acids research.
[11] E. Reddy,et al. EWS/Fli-1 chimeric protein is a transcriptional activator. , 1993, Cancer research.
[12] V. Nikodem,et al. hnRNP U Inhibits Carboxy-Terminal Domain Phosphorylation by TFIIH and Represses RNA Polymerase II Elongation , 1999, Molecular and Cellular Biology.
[13] S. Barnache,et al. The Transcription Factor Spi-1/PU.1 Interacts with the Potential Splicing Factor TLS* , 1998, The Journal of Biological Chemistry.
[14] M. Montminy,et al. Identification of a cyclic-AMP-responsive element within the rat somatostatin gene. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[15] M. Ouchida,et al. The EWS gene, involved in Ewing family of tumors, malignant melanoma of soft parts and desmoplastic small round cell tumors, codes for an RNA binding protein with novel regulatory domains. , 1994, Oncogene.
[16] G. Walter,et al. Monoclonal antibodies specific for the carboxy terminus of simian virus 40 large T antigen , 1984, Journal of virology.
[17] J. Pelletier,et al. The desmoplastic small round cell tumor t(11;22) translocation produces EWS/WT1 isoforms with differing oncogenic properties , 1998, Oncogene.
[18] K. A. Lee,et al. Transcriptional regulation by CREB and its relatives. , 1993, Biochimica et biophysica acta.
[19] D. Immanuel,et al. A topogenic role for the oncogenic N-terminus of TLS: nucleolar localization when transcription is inhibited , 1997, Oncogene.
[20] M. Montminy,et al. Protein-kinase-A-dependent activator in transcription factor CREB reveals new role for CREM repressers , 1993, Nature.
[21] N. Maizels,et al. A Specific Isoform of hnRNP D Interacts with DNA in the LR1 Heterodimer: Canonical RNA Binding Motifs in a Sequence-specific Duplex DNA Binding Protein* , 1998, The Journal of Biological Chemistry.
[22] T. Rabbitts,et al. Transcriptional activation by TAL1 and FUS-CHOP proteins expressed in acute malignancies as a result of chromosomal abnormalities. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[23] K. A. Lee,et al. The cellular transcription factor CREB corresponds to activating transcription factor 47 (ATF-47) and forms complexes with a group of polypeptides related to ATF-43 , 1990, Molecular and cellular biology.
[24] K. A. Lee,et al. Promoters containing ATF-binding sites are de-regulated in cells that express the EWS/ATF1 oncogene. , 1995, Oncogene.
[25] C. Denny,et al. The Ewing's sarcoma EWS/FLI-1 fusion gene encodes a more potent transcriptional activator and is a more powerful transforming gene than FLI-1 , 1993, Molecular and cellular biology.
[26] Kevin A. W. Lee,et al. MMSP tumor cells expressing the EWS/ATF1 oncogene do not support cAMP-inducible transcription , 1998, Oncogene.
[27] R. Lührmann,et al. Molecular cloning and subcellular localisation of the snRNP-associated protein 69KD, a structural homologue of the proto-oncoproteins TLS and EWS with RNA and DNA-binding properties. , 1996, Journal of molecular biology.
[28] Erica A Golemis,et al. Oncogenic EWS-Fli1 interacts with hsRPB7, a subunit of human RNA polymerase II , 1998, Oncogene.
[29] Jun Ma,et al. A new class of yeast transcriptional activators , 1987, Cell.
[30] C. Denny,et al. Multiple domains mediate transformation by the Ewing's sarcoma EWS/FLI-1 fusion gene. , 1995, Oncogene.
[31] F. Rauscher. Chromosome translocation-mediated conversion of a tumor suppressor gene into a dominant oncogene: fusion of EWS1 to WT1 in desmoplastic small round cell tumors. , 1997, Current topics in microbiology and immunology.
[32] C. Denny,et al. Biology of EWS/FLI and related fusion genes in Ewing's sarcoma and primitive neuroectodermal tumor. , 1997, Current topics in microbiology and immunology.
[33] G. McKnight,et al. Regulation of transcription by cyclic AMP-dependent protein kinase. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[34] M. Carey,et al. A synergistic increase in potency of a multimerized VP16 transcriptional activation domain. , 1992, The EMBO journal.
[35] G. Childs,et al. The Transcriptional Repressor ZFM1 Interacts with and Modulates the Ability of EWS to Activate Transcription* , 1998, The Journal of Biological Chemistry.
[36] D. Brow,et al. Control of pre-mRNA accumulation by the essential yeast protein Nrd1 requires high-affinity transcript binding and a domain implicated in RNA polymerase II association. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[37] M. Ouchida,et al. TLS/FUS fusion domain of TLS/FUS-erg chimeric protein resulting from the t(16;21) chromosomal translocation in human myeloid leukemia functions as a transcriptional activation domain. , 1994, Oncogene.
[38] M. Ouchida,et al. Inhibition of apoptosis by normal and aberrant Fli-1 and erg proteins involved in human solid tumors and leukemias , 1997, Oncogene.
[39] Hiroshi Handa,et al. NELF, a Multisubunit Complex Containing RD, Cooperates with DSIF to Repress RNA Polymerase II Elongation , 1999, Cell.
[40] D. Ron. TLS-CHOP and the role of RNA-binding proteins in oncogenic transformation. , 1997, Current topics in microbiology and immunology.
[41] P. Raychaudhuri,et al. trans-Activation by the hnRNP K Protein Involves an Increase in RNA Synthesis from the Reporter Genes (*) , 1996, The Journal of Biological Chemistry.
[42] K. Tanaka,et al. EWS-Fli1 antisense oligodeoxynucleotide inhibits proliferation of human Ewing's sarcoma and primitive neuroectodermal tumor cells. , 1997, The Journal of clinical investigation.
[43] M. Malim,et al. The VP16 transcription activation domain is functional when targeted to a promoter-proximal RNA sequence. , 1992, Genes & development.
[44] G. Thomas,et al. Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation. , 1993, Genomics.
[45] W. Schaffner,et al. C-terminal domain (CTD) of RNA-polymerase II and N-terminal segment of the human TATA binding protein (TBP) can mediate remote and proximal transcriptional activation, respectively. , 1993, Nucleic acids research.
[46] C. Denny,et al. Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[47] D. Storm,et al. The Prooncoprotein EWS Binds Calmodulin and Is Phosphorylated by Protein Kinase C through an IQ Domain* , 1997, The Journal of Biological Chemistry.
[48] D. L. Weeks,et al. Adenovirus E3-early promoter: sequences required for activation by E1A. , 1985, Nucleic acids research.
[49] M. Schemper,et al. EWS/FLI-1 antagonists induce growth inhibition of Ewing tumor cells in vitro. , 1996, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[50] William Arbuthnot Sir Lane,et al. Tyrosine kinase Pyk2 mediates G-protein-coupled receptor regulation of the Ewing sarcoma RNA-binding protein EWS , 1999, Current Biology.
[51] M. Ouchida,et al. Loss of tumorigenicity of Ewing's sarcoma cells expressing antisense RNA to EWS-fusion transcripts. , 1995, Oncogene.
[52] P. Chambon,et al. hTAF(II)68, a novel RNA/ssDNA‐binding protein with homology to the pro‐oncoproteins TLS/FUS and EWS is associated with both TFIID and RNA polymerase II. , 1996, The EMBO journal.
[53] G. Thomas,et al. EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts , 1993, Nature Genetics.
[54] J. Pelletier,et al. The DNA binding domains of the WT1 tumor suppressor gene product and chimeric EWS/WT1 oncoprotein are functionally distinct , 1998, Oncogene.