Androgen receptor specifically interacts with a novel p21-activated kinase, PAK6

被引:125
作者
Yang, F
Lio, XY
Sharma, MJ
Zarnegar, M
Lim, B
Sun, Z
机构
[1] Stanford Univ, Sch Med, Dept Surg, Liem Sioc Liong Mol Biol Lab, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Genet, Liem Sioc Liong Mol Biol Lab, Stanford, CA 94305 USA
[3] Beth Israel Deaconess Med Ctr, Dept Med, Div Hematol Oncol, Boston, MA 02215 USA
关键词
D O I
10.1074/jbc.M010311200
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 androgen receptor (AR) is a hormone-dependent transcription factor that plays important roles in male sexual differentiation and development. Transcription activation by steroid hormone receptors, such as the androgen receptor, is mediated through interaction with cofactors. We recently identified a novel AR-interacting protein, provisionally termed PAK6, that shares a high degree of sequence similarity with p21-activated kinases (PAKs). PAK6 is a 75-kDa protein that contains a putative amino-terminal Cdc42/Rac interactive binding motif and a carboxyl-terminal kinase domain. A domain-specific and ligand dependent interaction between AR and PAK6 was further confirmed in vivo and in vitro. Northern blot analysis revealed that PAK6 is highly expressed in testis and prostate tissues. Most importantly, immunofluorescence studies showed that PAK6 cotranslocates into the nucleus with AR in response to androgen, Transient transfection experiments showed that PAK6 specifically repressed AR-mediated transcription, This report identifies a novel function for a PAK-homologous protein and suggests a potential unique mechanism by which other signal transduction pathways may cross-talk with AR pathways to regulate AR function in normal and malignant prostate cells.
引用
收藏
页码:15345 / 15353
页数:9
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