The Deoxyribonucleic Acid Repair Protein Flap Endonuclease-1 Modulates Estrogen-Responsive Gene Expression

• Published in: Molecular endocrinology (Baltimore, Md.) Vol. 21; no. 7; pp. 1569 - 1580
• Main Authors: Schultz-Norton, Jennifer R, Walt, Kjirsten A, Ziegler, Yvonne S, McLeod, Ian X, Yates, John R, Raetzman, Lori T, Nardulli, Ann M
• Format: Journal Article
• Language: English
• Published: United States Endocrine Society 01.07.2007; Oxford University Press
• Subjects: Amino Acid Sequence; Animals; Base Sequence; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Cell Line, Tumor; DNA Repair; DNA, Complementary - genetics; Estradiol - pharmacology; Estrogen Receptor alpha - genetics; Estrogen Receptor alpha - metabolism; Female; Flap Endonucleases - genetics; Flap Endonucleases - metabolism; Gene Expression - drug effects; Humans; Mice; Mice, Inbred C57BL; Molecular Sequence Data; Ovariectomy; Recombinant Proteins - genetics; Recombinant Proteins - metabolism; RNA Interference; Uterus - drug effects; Uterus - metabolism
• ISSN: 0888-8809; 1944-9917
• DOI: 10.1210/me.2006-0519

The ligand-occupied estrogen receptor α (ERα) initiates changes in gene expression through its interaction with target DNA. The capacity of ERα to modulate gene expression is influenced by the association of the receptor with a variety of coregulatory proteins. To further understand the role of these coregulatory proteins in ERα-mediated transcription, we have isolated and identified proteins associated with ERα when it is bound to the consensus estrogen response element. One of the proteins identified in this complex, flap endonuclease-1 (FEN-1), is required for DNA replication and repair. We show that FEN-1 interacts directly with ERα and enhances the interaction of ERα with estrogen response element-containing DNA. More importantly, chromatin immunoprecipitation and RNA interference assays demonstrate that endogenously expressed FEN-1 associates with the native pS2 gene in MCF-7 cells and influences estrogen-responsive gene expression. Interestingly, estrogen differentially regulates expression of FEN-1 in mouse uterine epithelial, stromal, and myometrial cells. Together, our studies help to elucidate the functional consequence of the ERα-FEN-1 interaction and increase our understanding of the elaborate regulatory mechanisms that drive estrogen-responsive gene expression and DNA repair.