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ARA67/PAT1 functions as a repressor to suppress androgen receptor transactivation.


ABSTRACT: The androgen receptor (AR) may recruit multiple coregulators for proper or optimal transactivation. Here we report the identification and characterization of ARA67/PAT1 as an AR coregulator from a prostate cDNA library. ARA67/PAT1 was screened out as an AR N terminus interacting protein. Interaction mapping shows that the cooperation of multiple domains within ARA67/PAT1 may be required for the maximal interaction with AR. ARA67/PAT1 functions as a repressor with better suppressive effects on AR compared to glucocorticoid receptor and estrogen receptor. Further mechanism dissection reveals that the interrupted AR cytoplasmic-nuclear shuttling may play a major role in ARA67/PAT1 mediated suppression on AR. Together, these results suggest that ARA67/PAT1 may function as a novel repressor that can modulate AR function in prostate cancer.

SUBMITTER: Zhang Y 

PROVIDER: S-EPMC321420 | biostudies-literature | 2004 Feb

REPOSITORIES: biostudies-literature

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ARA67/PAT1 functions as a repressor to suppress androgen receptor transactivation.

Zhang Yanqing Y   Yang Yue Y   Yeh Shuyuan S   Chang Chawnshang C  

Molecular and cellular biology 20040201 3


The androgen receptor (AR) may recruit multiple coregulators for proper or optimal transactivation. Here we report the identification and characterization of ARA67/PAT1 as an AR coregulator from a prostate cDNA library. ARA67/PAT1 was screened out as an AR N terminus interacting protein. Interaction mapping shows that the cooperation of multiple domains within ARA67/PAT1 may be required for the maximal interaction with AR. ARA67/PAT1 functions as a repressor with better suppressive effects on AR  ...[more]

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