McMahon S B, Van Buskirk H A, Dugan K A, Copeland T D, Cole M D
Department of Molecular Biology, Princeton University, New Jersey 08544-1014, USA.
Cell. 1998 Aug 7;94(3):363-74. doi: 10.1016/s0092-8674(00)81479-8.
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.
c-Myc和E2F转录因子是高等真核生物细胞周期进程中最有力的调节因子。本报告描述了一种新型的、高度保守的434 kDa蛋白质的分离,该蛋白质命名为TRRAP,它与c-Myc的N末端特异性相互作用,并且与ATM/PI3激酶家族具有同源性。TRRAP也与E2F-1反式激活结构域特异性相互作用。TRRAP蛋白的反式显性突变体或反义RNA的表达可阻断c-Myc和E1A介导的致癌转化。这些数据表明,TRRAP是c-Myc和E1A/E2F致癌转录因子途径的必需辅因子。