Interaction of Estrogen Receptor α with 3-Methyladenine DNA Glycosylase Modulates Transcription and DNA Repair

• Published in: The Journal of biological chemistry 2004-04, Vol.279 (16), p.16875-16882
• Main Authors: Likhite, Varsha S., Cass, Emily I., Anderson, Scott D., Yates, John R., Nardulli, Ann M.
• Format: Article
• Language: English
• Subjects: DNA Glycosylases - genetics; DNA Glycosylases - metabolism; DNA Repair; Estrogen Receptor alpha; HeLa Cells; Humans; Protein Binding; Receptors, Estrogen - metabolism; Signal Transduction - genetics; Transcription, Genetic
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M313155200

Estrogen receptor α (ERα) interacts with basal transcription factors, coregulatory proteins, and chromatin modifiers to initiate transcription of the target genes. We have identified a novel interaction between ERα and the DNA repair protein 3-methyladenine DNA glycosylase (MPG) thereby providing a functional link between gene expression and DNA repair. Interestingly, the ERα-MPG interaction was enhanced by the presence of estrogen response element (ERE)-containing DNA. In vitro pull-down assays indicated that the interaction of ERα with MPG was direct and occurred through the DNA- and ligand-binding domains and the hinge region of the receptor. More importantly, endogenously expressed ERα and MPG from MCF-7 cells coimmunoprecipitated with ERα- and MPG-specific antibodies. The ERα-MPG interaction had functional consequences on the activities of both proteins. ERα increased MPG acetylation, stabilized the binding of MPG with hypoxanthine-containing oligos, and enhanced MPG-catalyzed removal of hypoxanthine from DNA. In turn, MPG dramatically stabilized the interaction of ERα with ERE-containing oligos, decreased p300-mediated acetylation of the receptor, and reduced transcription of simple and complex ERE-containing reporter plasmids in a dose-dependent manner. Our studies suggest that recruitment of MPG to ERE-containing genes influences transcription and plays a role in maintaining integrity of the genome by recruiting DNA repair proteins to actively transcribing DNA.