Inhibition of histone deacetylation augments dihydrotestosterone inductionof androgen receptor levels: An explanation for trichostatin A effects on androgen-induced chromatin remodeling and transcription of the mouse mammary tumor virus promoter

The integrated mouse mammary tumor virus (MMTV) promoter has provided an ex cellent model system with which to study the impact of steroid hormones on transcriptional activation in the context of a defined chromatin structure. The hormone response element (HRE) of this promoter is positioned on a pha sed nucleosome which becomes remodeled in response to steroids. One possibl e mechanism of chromatin remodeling by steroid receptors could involve recr uitment of coactivators which alter the histone acetylation status of the H RE nucleosome. To examine how the androgen receptor (AR) influences transcr iption and chromatin remodeling and to assess whether changes in histone ac etylation are involved in these effects, we determined whether the specific histone deacetylase inhibitor trichostatin A (TSA) influenced basal- and a ndrogen-mediated transcriptional activation of the integrated MMTV promoter in the mouse L-cell fibroblast cell line 29+. These cells harbor the MMTV promoter integrated in the genome and express only one steroid hormone rece ptor subtype, i.e., the AR. Surprisingly, we found that treatment of the ce lls with TSA alone had virtually no effect on transcription and chromatin r emodeling of the MMTV promoter nor on AR levels. However, pretreatment with TSA augmented the DHT effects on all three parameters. These results sugge st that histone acetylation changes at the MMTV B nucleosome per se are not alone sufficient to induce chromatin remodeling and subsequent induction o f MMTV transcription. Rather, the histone deacetylase inhibitor TSA exerts a portion of its effect on MMTV chromatin remodeling and transcriptional ac tivation indirectly through increases in AR levels. (C) 1999 Academic Press .