EWS-ATF-1 chimeric protein in soft tissue clear cell sarcoma associates with CREB-binding protein and interferes with p53-mediated trans-activation function
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Fujimura, Y
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机构:Med Coll Penn & Hahnemann Univ, Sch Med, Program Canc Genet, Canc Ctr,Dept Biochem, Philadelphia, PA 19102 USA
Fujimura, Y
Siddique, H
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机构:Med Coll Penn & Hahnemann Univ, Sch Med, Program Canc Genet, Canc Ctr,Dept Biochem, Philadelphia, PA 19102 USA
Siddique, H
Lee, L
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机构:Med Coll Penn & Hahnemann Univ, Sch Med, Program Canc Genet, Canc Ctr,Dept Biochem, Philadelphia, PA 19102 USA
Lee, L
Rao, VN
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机构:Med Coll Penn & Hahnemann Univ, Sch Med, Program Canc Genet, Canc Ctr,Dept Biochem, Philadelphia, PA 19102 USA
Rao, VN
Reddy, ESP
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机构:Med Coll Penn & Hahnemann Univ, Sch Med, Program Canc Genet, Canc Ctr,Dept Biochem, Philadelphia, PA 19102 USA
Reddy, ESP
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[1] Med Coll Penn & Hahnemann Univ, Sch Med, Program Canc Genet, Canc Ctr,Dept Biochem, Philadelphia, PA 19102 USA
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.