| Literature DB >> 9708738 |
S B McMahon1, H A Van Buskirk, K A Dugan, T D Copeland, M D Cole.
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.Entities:
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Year: 1998 PMID: 9708738 DOI: 10.1016/s0092-8674(00)81479-8
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582