Potentiation of estrogen receptor transcriptional activity by breast cancer amplified sequence 2

被引:30
作者
Qi, C [1 ]
Zhu, YT [1 ]
Chang, J [1 ]
Yeldandi, AV [1 ]
Rao, MS [1 ]
Zhu, YJ [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Pathol, Chicago, IL 60611 USA
关键词
breast cancer amplified sequence 2; coactivator; estrogen receptor alpha;
D O I
10.1016/j.bbrc.2004.12.187
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
Breast cancer amplified sequence 2 (BCAS2) was initially identified as a gene that was overexpressed and amplified in some breast cancer cell lines. It was later found to be a component of the spliceosome. Here, we identified BCAS2 as an estrogen receptor (ER) alpha interacting protein by yeast two-hybrid screening. In addition to ERalpha, BCAS2 also interacted with ERbeta, TRbeta, PR, and PPARgamma in a ligand-independent way. Transient transfection assays revealed that overexpression of BCAS2 enhanced while inhibition of BCAS2 expression attenuated the estrogen receptor-mediated transcription. BCAS2 potentiated the activation function-2 (AF-2) activity of ERalpha but had no effect on the AF-1 activity. This study suggested that BCAS2 might play an important role in breast cancer development by increasing the estrogen receptor's function. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:393 / 398
页数:6
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