The tri-nucleotide spacer sequence between estrogen response element half-sites is conserved and modulates ERα-mediated transcriptional responses
| Autor: | Caleb B. Kallen, Neil Sidell, Danzhou Yang, Feng jue Shu |
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| Rok vydání: | 2010 |
| Předmět: |
Transcription
Genetic Endocrinology Diabetes and Metabolism Clinical Biochemistry Response element Estrogen receptor Biology Response Elements Biochemistry Article Cell Line Transactivation Endocrinology Cell Line Tumor Consensus sequence Humans Enhancer Molecular Biology Hormone response element Estrogen Receptor alpha Nucleic acid sequence Estrogens Cell Biology Molecular biology Genetic Loci Molecular Medicine Estrogen receptor alpha hormones hormone substitutes and hormone antagonists Protein Binding |
| Zdroj: | The Journal of Steroid Biochemistry and Molecular Biology. 120:172-179 |
| ISSN: | 0960-0760 |
| DOI: | 10.1016/j.jsbmb.2010.04.009 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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