SENP1 enhances androgen receptor-dependent transcription through desumoylation of histone deacetylase 1

Mol Cell Biol. 2004 Jul;24(13):6021-8. doi: 10.1128/MCB.24.13.6021-6028.2004.

Abstract

SUMO (also called Sentrin) is a ubiquitin-like protein that plays an important role in regulating protein function and localization. It is known that several nuclear receptors are modified by SUMO; however, the effect of desumoylation in regulating nuclear receptor function has not been elucidated. Here we show that androgen receptor (AR)-mediated transcription is markedly enhanced by SENP1, a member of SUMO-specific protease family. SENP1's ability to enhance AR-dependent transcription is not mediated through desumoylation of AR, but rather through its ability to deconjugate histone deacetylase 1 (HDAC1), thereby reducing its deacetylase activity. HDAC1's repressive effect on AR-dependent transcription could be reversed by SENP1 and by deletion of its sumoylation sites. RNA interference depletion of endogenous HDAC1 also reduced SENP1's effect. Thus, SENP1 could regulate AR-dependent transcription through desumoylation of HDAC1. These studies provide insights on the potential role of desumoylation in the regulation of nuclear receptor activity.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Line, Tumor
  • Cysteine Endopeptidases
  • Endopeptidases / physiology*
  • Gene Expression Regulation
  • Histone Deacetylase 1
  • Histone Deacetylases / genetics
  • Histone Deacetylases / metabolism*
  • Humans
  • RNA, Small Interfering / pharmacology
  • Receptors, Androgen / physiology*
  • Receptors, Cytoplasmic and Nuclear
  • SUMO-1 Protein / metabolism
  • Transcription, Genetic*
  • Ubiquitins / metabolism

Substances

  • RNA, Small Interfering
  • Receptors, Androgen
  • Receptors, Cytoplasmic and Nuclear
  • SUMO-1 Protein
  • Ubiquitins
  • Endopeptidases
  • SENP1 protein, human
  • Cysteine Endopeptidases
  • HDAC1 protein, human
  • Histone Deacetylase 1
  • Histone Deacetylases