Hormone-Dependent Coactivator Binding to a Hydrophobic Cleft on Nuclear Receptors

Author:

Feng Weijun123,Ribeiro Ralff C. J.123,Wagner Richard L.123,Nguyen Hoa123,Apriletti James W.123,Fletterick Robert J.123,Baxter John D.123,Kushner Peter J.123,West Brian L.123

Affiliation:

1. W. Feng, H. Nguyen, J. W. Apriletti, J. D. Baxter, P. J. Kushner, B. L. West, Metabolic Research Unit, Box 0540, University of California San Francisco, San Francisco, CA 94143–0540, USA.

2. R. C. J. Ribeiro, Department of Pharmaceutical Sciences, University of Brasilia, D.F., Brazil.

3. R. L. Wagner and R. J. Fletterick, Department of Biochemistry and Biophysics, S1058, University of California San Francisco, San Francisco, CA 94143, USA.

Abstract

The ligand-binding domain of nuclear receptors contains a transcriptional activation function (AF-2) that mediates hormone-dependent binding of coactivator proteins. Scanning surface mutagenesis on the human thyroid hormone receptor was performed to define the site that binds the coactivators, glucocorticoid receptor–interacting protein 1 (GRIP1) and steroid receptor coactivator 1 (SRC-1). The residues involved encircle a small surface that contains a hydrophobic cleft. Ligand activation of transcription involves formation of this surface by folding the carboxyl-terminal α helix against a scaffold of three other helices. These features may represent general ones for nuclear receptors.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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