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Originally published In Press as doi:10.1074/jbc.M106354200 on March 13, 2002

J. Biol. Chem., Vol. 277, Issue 20, 17781-17788, May 17, 2002
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Androgen Receptor-interacting Protein 3 and Other PIAS Proteins Cooperate with Glucocorticoid Receptor-interacting Protein 1 in Steroid Receptor-dependent Signaling*

Noora KotajaDagger , Marianne VihinenDagger , Jorma J. PalvimoDagger §, and Olli A. JänneDagger ||

From the Dagger  Biomedicum Helsinki, Institute of Biomedicine (Physiology), § Institute of Biotechnology, and the  Department of Clinical Chemistry, University of Helsinki and Helsinki University Central Hospital, Helsinki FIN-00014, Finland

Androgen receptor (AR)-interacting protein 3 (ARIP3/PIASxalpha ) is a coregulator capable of modulating transcriptional activity of various steroid receptors. We have characterized functional regions of ARIP3 and studied its interaction with the glucocorticoid receptor (GR)-interacting protein 1 (GRIP1). We find that the potential zinc-binding domain is critical for ARIP3 to function as a coactivator; the deletion of amino acids 347-418 or the mutation of the conserved cysteines 385 and 388 to serines converts ARIP3 to a transcriptional repressor from AR-dependent minimal promoters and abolishes its ability to activate GR. By contrast, mutations in the two LXXLL motifs of ARIP3 have relatively minor effects on its ability to regulate AR or GR function. ARIP3 is able to interact with different regions of GRIP1, but the strongest interaction is detected with the C-terminal region (amino acids 1122-1462) of GRIP1. The interaction of ARIP3 with the latter GRIP1 domain or full-length GRIP1 and the ability of ARIP3 to cooperate with GRIP1 in the regulation of AR- or GR-dependent transcription are dependent on the ARIP3 zinc-binding region. We also find a strong synergism between GRIP1 and two other PIAS family members, Miz1 and PIAS1. Taken together, our results suggest that PIAS proteins and GRIP1 interact functionally in transcriptional regulation.

* This work was supported by grants from the Medical Research Council (Academy of Finland), the Finnish Foundation for Cancer Research, the Sigrid Jusélius Foundation, Biocentrum Helsinki, the Helsinki University Central Hospital, and Association for the Cure of Cancer of Prostate.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

|| To whom correspondence should be addressed: Biomedicum Helsinki, Institute of Biomedicine, University of Helsinki, P.O. Box 63, FIN-00014 Helsinki, Finland. Tel.: 358-9-191-25040; Fax: 358-9-191-25047; E-mail: olli.janne@helsinki.fi.

Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.


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