EWS-ATF-1 chimeric protein in soft tissue clear cell sarcoma associates with CREB-binding protein and interferes with p53-mediated trans-activation function

被引:27
作者
Fujimura, Y
Siddique, H
Lee, L
Rao, VN
Reddy, ESP
机构
[1] Med Coll Penn & Hahnemann Univ, Sch Med, Program Canc Genet, Canc Ctr,Dept Biochem, Philadelphia, PA 19102 USA
[2] SAIC, Frederick, MD 21702 USA
关键词
EWS-ATF-1; CBP; p53; Ewing's sarcoma; clear cell sarcoma;
D O I
10.1038/sj.onc.1204684
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The recurrent t(12;22) (q13;q12) chromosomal translocation associated with soft tissue clear cell sarcoma results in a chimeric protein EWS-ATF-1 that acts as a constitutive transcriptional activator. The CBP/p300 transcriptional coactivator, which links various transcriptional factors to basal transcription apparatus, participates in transcriptional activation, growth and cell cycle control and differentiation. In this study, we show that EWS-ATF-1 associates constitutively with CBP both in vitro and in vivo. Both EWS and ATF-1 fusion domains are needed for this interaction. Here, we demonstrate that EWS-ATF-1 represses p53/CBP-mediated transactivation function. Overexpression of CBP can counteract this repressive effect of EWS-ATF-1. Taken together, these findings suggest that one of the mechanisms by which EWS-ATF-1 may cause tumors is through targeting CBP/p300 resulting in the loss of function of p53. This novel mechanism may be responsible for the development of these and other related solid tumors.
引用
收藏
页码:6653 / 6659
页数:7
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