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Cyclin D1 Binds the Androgen Receptor and Regulates Hormone-Dependent Signaling in a p300/CBP-Associated Factor (P/CAF)-Dependent Manner
- Source :
- Molecular Endocrinology. 15:797-811
- Publication Year :
- 2001
- Publisher :
- The Endocrine Society, 2001.
-
Abstract
- The androgen receptor (AR) is a ligand-regulated member of the nuclear receptor superfamily. The cyclin D1 gene product, which encodes the regulatory subunit of holoenzymes that phosphorylate the retinoblastoma protein (pRB), promotes cellular proliferation and inhibits cellular differentiation in several different cell types. Herein the cyclin D1 gene product inhibited ligand-induced AR- enhancer function through a pRB-independent mechanism requiring the cyclin D1 carboxyl terminus. The histone acetyltransferase activity of P/CAF (p300/CBP associated factor) rescued cyclin D1-mediated AR trans-repression. Cyclin D1 and the AR both bound to similar domains of P/CAF, and cyclin D1 displaced binding of the AR to P/CAF in vitro. These studies suggest cyclin D1 binding to the AR may repress ligand-dependent AR activity by directly competing for P/CAF binding.
- Subjects :
- Male
Cyclin E
Cyclin D
Blotting, Western
Molecular Sequence Data
Cyclin A
Cell Cycle Proteins
Ligands
03 medical and health sciences
0302 clinical medicine
Endocrinology
Cyclin D1
Acetyltransferases
Androgen Receptor Antagonists
Tumor Cells, Cultured
Humans
Histone acetyltransferase activity
p300-CBP Transcription Factors
Amino Acid Sequence
Molecular Biology
Histone Acetyltransferases
030304 developmental biology
Cyclin
0303 health sciences
biology
Prostatic Neoplasms
General Medicine
Molecular biology
Receptors, Androgen
030220 oncology & carcinogenesis
Mutation
biology.protein
Cyclin-dependent kinase complex
Sequence Alignment
Cyclin A2
Signal Transduction
Transcription Factors
Subjects
Details
- ISSN :
- 19449917 and 08888809
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Molecular Endocrinology
- Accession number :
- edsair.doi.dedup.....15d2cbb7632d8298b04e97e07bd3e99c
- Full Text :
- https://doi.org/10.1210/mend.15.5.0641