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J. Biol. Chem., Vol. 280, Issue 8, 6721-6730, February 25, 2005

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Ubc9 and Protein Inhibitor of Activated STAT 1 Activate Chicken Ovalbumin Upstream Promoter-Transcription Factor I-mediated Human CYP11B2 Gene Transcription^*

Isao Kurihara, Hirotaka Shibata¶, Sakiko Kobayashi, Noriko Suda, Yayoi Ikeda||, Kenichi Yokota, Ayano Murai, Ikuo Saito, William E. Rainey**, and Takao Saruta

From the Department of Internal Medicine, School of Medicine, Keio University, Tokyo 160-8582, Japan, the Health Center, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, the ^||Department of Fine Morphology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan, and the ^**Division of Reproductive Endocrinology, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9032

Aldosterone synthase (CYP11B2) is involved in the final steps of aldosterone biosynthesis and expressed exclusively in the adrenal zona glomerulosa cells. Using an electrophoretic mobility shift assay, we demonstrate that COUP-TFI binds to the –129/–114 element (Ad5) of human CYP11B2 promoter. Transient transfection in H295R adrenal cells demonstrated that COUP-TFI enhanced CYP11B2 reporter activity. However, the reporter construct with mutated Ad5 sequences showed reduced basal and COUP-TFI-enhanced activity, suggesting that binding of COUP-TFI to Ad5 is important for CYP11B2 transactivation. To elucidate molecular mechanisms of COUP-TFI-mediated activity, we subsequently screened for COUP-TFI-interacting proteins from a human adrenal cDNA library using a yeast two-hybrid system and identified Ubc9 and PIAS1, which have small ubiquitin-related modifier-1 (SUMO-1) conjugase and ligase activities, respectively. The coimmunoprecipitation assays confirmed that COUP-TFI forms a complex with Ubc9 and PIAS1 in mammalian cells. Immunohistochemistry showed that Ubc9 and PIAS1 are markedly expressed in rat adrenal glomerulosa cells. Coexpression of Ubc9 and PIAS1 synergistically enhanced the COUP-TFI-mediated CYP11B2 reporter activity, indicating that both proteins function as coactivators of COUP-TFI. However, sumoylation-defective mutants, Ubc9 (C93S) and PIAS1 (C351S), continued to function as coactivators of COUP-TFI, indicating that sumoylation activity are separable from coactivator ability. In addition, chromatin immunoprecipitation assays demonstrated that ectopically expressed COUP-TFI, Ubc9, and PIAS1 were recruited to an endogenous CYP11B2 promoter. Moreover, reduction of Ubc9 or PIAS1 protein levels by small interfering RNA inhibited the CYP11B2 transactivation by COUP-TFI. Our data support a physiological role of Ubc9 and PIAS1 as transcriptional coactivators in COUP-TFI-mediated CYP11B2 transcription.

Received for publication, October 18, 2004 , and in revised form, December 14, 2004.

^* This work was supported by a Grant-in-Aid for Scientific Research (C) from the Japan Society for the Promotion of Science (No. 14571072, 2002-4) (to H. S.), by a Grant-in-Aid for Research Project for Disorders of Adrenocortical Hormone Production from the Ministry of Health, Labor and Welfare, Japan (to T. S.), and by Grant DK043140 from the National Institutes of Health (to W. E. R.). The costs of publication of this article were defrayed in part by the payment of page charges. This 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. Tel.: 81-3-3353-1211 (ext. 62312); Fax: 81-3-5363-3635; E-mail: hiro-405{at}cb3.so-net.ne.jp.

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