The tri-nucleotide spacer sequence between estrogen response element half-sites is conserved and modulates ERalpha-mediated transcriptional responses

• Type of Material: Article
• Authors: Feng-jue Shu, Emory University; Neil Sidell, Emory University; Danzhou Yang, The University of Arizona; Caleb B. Kallen, Emory University
• Language: English
• Date: 2010-06
• Publisher: Elsevier: 12 months
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2010 Elsevier Ltd. All rights reserved.
• License: Creative Commons Attribution-NonCommerical-NoDerivs 3.0 Unported
• Final Published Version (URL): http://dx.doi.org/10.1016/j.jsbmb.2010.04.009
• Title of Journal or Parent Work: Journal of Steroid Biochemistry and Molecular Biology
• ISSN: 0960-0760
• Volume: 120
• Issue: 4-5
• Start Page: 172
• End Page: 179
• Grant/Funding Information: This work was supported by the Research Scientist Development Program/NIH K12-HD000849 (to CBK) and the NIH R01-CA129424 (to NS).
• Keywords: estrogen receptor; estrogen response element; tri-nucleotide spacer; estrogen
• Research Categories: Biology, Molecular; Chemistry, Biochemistry; Health Sciences, Obstetrics and Gynecology

Abstract

The estrogen response element (ERE) consensus sequence is AGGTCAnnnTGACCT, where nnn is known as the tri-nucleotide spacer sequence. Studying 1017 high-confidence ERα-bound loci, we found that genomic EREs are enriched for spacers composed of C(A/T)G, suggesting that the spacer may influence receptor binding and transcriptional responses. We designed consensus EREs containing variable spacer sequences and compared ERα binding in gel shift assays and enhancer function in reporter assays. We found that ERα-ERE binding affinity is modulated by the tri-nucleotide spacer sequence and is favored by spacer sequences of CTG > GCC > TTT. Similarly, luciferase reporter assays indicated that the estrogen-stimulated transcriptional response is modulated by the spacer and parallels the gel shift data: CTG > GCC > TTT. Reporter assays demonstrated that the spacer sequence also modulates the sensitivity of EREs to repression engendered by the receptor antagonist hydroxytamoxifen. These experiments indicate that the sequence of the tri-nucleotide spacer is non-random at receptor-bound genomic loci, influences ERα-DNA binding affinity, and modulates transactivation potential of the receptor-ligand-DNA complex. This work has implications for understanding which genomic EREs are targeted by ERα, should improve computational prediction of functional EREs within genomic sequences, and describes novel sequence determinants of the estrogen response.