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Loss of androgen receptor transcriptional activity at the G(1)/S transition
Elisabeth D Martinez1, Mark Danielsen
1Department of Biochemistry and Molecular Biology, Georgetown University School of Medicine, Washington, D. C. 20007, USA.
Abstract:
Androgens are essential for the differentiation, growth, and maintenance of male-specific organs. The effects of androgens in cells are mediated by the androgen receptor (AR), a member of the nuclear receptor superfamily of transcription factors. Recently, transient transfection studies have shown that overexpression of cell cycle regulatory proteins affects the transcriptional activity of the AR. In this report, we characterize the transcriptional activity of endogenous AR through the cell cycle. We demonstrate that in G0, AR enhances transcription from an integrated steroid-responsive mouse mammary tumor virus promoter and also from an integrated androgen-specific probasin promoter. This activity is strongly reduced or abolished at the G(1)/S boundary. In S phase, the receptor regains activity, indicating that there is a transient regulatory event that inactivates the AR at the G(1)/S transition. This regulation is specific for the AR, since the related glucocorticoid receptor is transcriptionally active at the G(1)/S boundary. Not all of the effects of androgens are blocked, however, since androgens retain the ability to increase AR protein levels. The transcriptional inactivity of the AR at the G(1)/S junction coincides with a decrease in AR protein level, although activity can be partly rescued without an increase in receptor. Inhibition of histone deacetylases brings about this partial restoration of AR activity at the G(1)/S boundary, demonstrating the involvement of acetylation pathways in the cell cycle regulation of AR transcriptional activity. Finally, a model is proposed that explains the inactivity of the AR at the G(1)/S transition by integrating receptor levels, the action of cell cycle regulators, and the contribution of histone acetyltransferase-containing coactivators.
Insights
Androgen receptor (AR) activity is reduced at the G1/S cell cycle boundary, impacting gene transcription. This regulation involves AR protein levels and histone deacetylase inhibition, offering insights into androgen signaling.
Area of Science:
- Molecular Biology
- Cell Biology
- Endocrinology
Background:
- Androgens are crucial for male development and function.
- The androgen receptor (AR) mediates androgen effects by regulating gene transcription.
- Cell cycle regulatory proteins can influence AR transcriptional activity.
Purpose of the Study:
- To investigate the cell cycle-dependent transcriptional activity of the endogenous androgen receptor (AR).
- To elucidate the mechanisms regulating AR activity during the cell cycle, particularly at the G1/S transition.
Main Methods:
- Characterization of endogenous AR transcriptional activity across the cell cycle using integrated reporter gene assays (mouse mammary tumor virus and probasin promoters).
- Analysis of AR protein levels and their correlation with transcriptional activity.
- Investigation of the effect of histone deacetylase inhibition on AR activity at the G1/S boundary.
Main Results:
- AR enhances transcription in G0 phase, but this activity is significantly reduced or abolished at the G1/S boundary.
- AR regains transcriptional activity in S phase, indicating a transient regulatory event.
- AR activity is specifically regulated at the G1/S transition, unlike the glucocorticoid receptor.
- Androgens increase AR protein levels, and AR inactivity at G1/S coincides with decreased AR protein.
- Inhibition of histone deacetylases partially restores AR activity at the G1/S boundary.
Conclusions:
- The androgen receptor's transcriptional activity is tightly regulated throughout the cell cycle, with a specific inactivation at the G1/S transition.
- This cell cycle regulation involves changes in AR protein levels and epigenetic modifications, specifically histone acetylation.
- A model integrating receptor levels, cell cycle regulators, and coactivator complexes explains AR inactivity at the G1/S junction.