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Investigation on the potential role of the Ah receptor nuclear translocator protein in vitamin D receptor action.

作者信息

Reisz-Porszasz S, Reyes H, DeLuca H F, Prahl J M, Hankinson O

机构信息

Laboratory of Biomedical and Environmental Sciences, University of California, Los Angeles.

出版信息

J Recept Res. 1993;13(8):1147-59. doi: 10.3109/10799899309063269.

Abstract

The Ah receptor nuclear translocator protein (ARNT) is required for binding of the Ah (dioxin) receptor to the xenobiotic responsive element (XRE), and is a structural component of the XRE-binding form of the Ah receptor. The vitamin D receptor requires an accessory protein for binding to the vitamin D responsive element (VDRE) in the osteocalcin gene. Since the vitamin D receptor has similarities to the Ah receptor, we investigated whether ARNT is also required for vitamin D receptor activity. Two lines of evidence demonstrate that ARNT is not required for vitamin D receptor activity, and therefore does not correspond to the vitamin D receptor accessory protein: i) Antibodies to ARNT have no effect on binding of the vitamin D receptor to the VDRE. ii) c4, a mutant of Hepa-1 cells that is defective in ARNT activity, and in which binding of the Ah receptor to the XRE does not occur, possesses a vitamin D receptor with full activity for binding the VDRE.

摘要

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