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Genes to Cells (2007) 12, 1281-1287. doi:10.1111/j.1365-2443.2007.01131.x
© 2007 Blackwell Publishing or its licensors

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A reduction state potentiates the glucocorticoid response through receptor protein stabilization

Hirochika Kitagawa1, Ikuko Yamaoka1,2, Chihiro Akimoto1, Ikuko Kase1, Yoshihiro Mezaki1, Takafumi Shimizu1 and Shigeaki Kato1,2,*

1 The Institute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo, 113-0032, Japan
2 ERATO, Japan Science and Technology Agency, Kawaguchi, Saitama 332-0012, Japan

The intracellular redox state regulates all biological processes including gene expression. The glucocorticoid receptor (GR), a hormone-dependent transcription factor, is affected by the redox state. GR translocation from the cytoplasm to the nucleus is regulated by oxidative stress. The molecular mechanism of how the redox state affects GR transcriptional regulation, however, has not been clarified. We identified a deoxidizing agent, cobalt chloride (CoCl2), that potentiates the GR transcriptional effects by stabilizing endogenously expressed GR protein as well as exogenously over-expressed one without affecting GR mRNA level. Consequent GR protein stabilization enhanced co-factor recruitments on the target gene promoters. These results support the existence of a novel redox-dependent mechanism of GR transcriptional regulation mediated by receptor protein stabilization.


Communicated by: Kohei Miyazono

* Correspondence: E-mail: uskato{at}mail.ecc.u-tokyo.ac.jp







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