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Cell ; 94(3): 363-74, 1998 Aug 07.
Article in English | MEDLINE | ID: mdl-9708738

ABSTRACT

The c-Myc and E2F transcription factors are among the most potent regulators of cell cycle progression in higher eukaryotes. This report describes the isolation of a novel, highly conserved 434 kDa protein, designated TRRAP, which interacts specifically with the c-Myc N terminus and has homology to the ATM/PI3-kinase family. TRRAP also interacts specifically with the E2F-1 transactivation domain. Expression of transdominant mutants of the TRRAP protein or antisense RNA blocks c-Myc- and E1A-mediated oncogenic transformation. These data suggest that TRRAP is an essential cofactor for both the c-Myc and E1A/E2F oncogenic transcription factor pathways.


Subject(s)
Carrier Proteins , Cell Cycle Proteins , DNA-Binding Proteins , Nuclear Proteins/physiology , Protein Serine-Threonine Kinases , Proteins/physiology , Proto-Oncogene Proteins c-myc/physiology , Transcription Factors/physiology , Adaptor Proteins, Signal Transducing , Adenovirus E1A Proteins/genetics , Adenovirus E1A Proteins/physiology , Amino Acid Sequence , Ataxia Telangiectasia Mutated Proteins , Cell Transformation, Neoplastic/drug effects , Cell Transformation, Neoplastic/genetics , Cell Transformation, Neoplastic/pathology , Conserved Sequence , DNA, Complementary/isolation & purification , E2F Transcription Factors , E2F1 Transcription Factor , Evolution, Molecular , Genes, Dominant , HeLa Cells , Humans , Molecular Sequence Data , Mutagenesis, Site-Directed , Nuclear Proteins/chemistry , Nuclear Proteins/genetics , Oligonucleotides, Antisense/pharmacology , Phosphatidylinositol 3-Kinases/chemistry , Protein Binding , Retinoblastoma-Binding Protein 1 , Transcription Factor DP1 , Tumor Suppressor Proteins
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