Estrogen receptor alpha regulates expression of the breast cancer 1 associated ring domain 1 (BARD1) gene through intronic DNA sequence.
Mol Cell Endocrinol
; 267(1-2): 106-15, 2007 Mar 15.
Article
en En
| MEDLINE
| ID: mdl-17275994
ABSTRACT
We have used a chromatin immunoprecipitation (ChIP)-based cloning strategy to isolate and identify genes associated with estrogen receptor alpha (ERalpha) in MCF-7 human breast cancer cells. One of the gene regions isolated was a 288bp fragment from the ninth intron of the breast cancer 1 associated ring domain (BARD1) gene. We demonstrated that ERalpha associated with this region of the endogenous BARD 1 gene in MCF-7 cells, that ERalpha bound to three of five ERE half sites located in the 288bp BARD1 region, and that this 288bp BARD1 region conferred estrogen responsiveness to a heterologous promoter. Importantly, treatment of MCF-7 cells with estrogen increased BARD1 mRNA and protein levels. These findings demonstrate that ChIP cloning strategies can be utilized to successfully isolate regulatory regions that are far removed from the transcription start site and assist in identifying cis elements involved in conferring estrogen responsiveness.
Texto completo:
1
Colección:
01-internacional
Asunto principal:
Intrones
/
Regulación Neoplásica de la Expresión Génica
/
Proteínas Supresoras de Tumor
/
Ubiquitina-Proteína Ligasas
/
Receptor alfa de Estrógeno
Tipo de estudio:
Prognostic_studies
/
Risk_factors_studies
Límite:
Humans
Idioma:
En
Revista:
Mol Cell Endocrinol
Año:
2007
Tipo del documento:
Article
País de afiliación:
Estados Unidos