Estrogen Receptor has Enhanced Affinity for Bromodeoxyuridine-Substituted DNA

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 75; no. 10; pp. 4896 - 4900
• Main Authors: Kallos, John, Fasy, Thomas M., Hollander, Vincent P., Bick, Michael D.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences of the United States of America 01-10-1978; National Acad Sciences
• Subjects: Animals; Atoms; Binding, Competitive; Biochemistry; Bromine; Bromodeoxyuridine - metabolism; Cell lines; DNA; DNA - metabolism; Estrogen receptors; Genetic equilibrium; Kinetics; Rabbits; Radioactive decay; Receptors; Receptors, Estrogen - metabolism
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.75.10.4896

The estrogen receptor (E2R) from rabbit uterus has an enhanced affinity for BrdUrd-substituted DNA compared to unsubstituted DNA. Increasing levels of BrdUrd substitution (from 0 to 100%) in a DNA sample are associated with increasingly tighter binding of E2R to that DNA as measured by equilibrium competition experiments and by rates of dissociation (or receptor transfer experiments). Although the rates of dissociation of E2R· DNA complexes vary greatly, depending on the BrdUrd-substitution level in the DNA, no differences were detected between the rates of association of E2R with unsubstituted and fully BrdUrd-substituted DNA. The E2R· DNA complex dissociates more rapidly in 150 mM KCl than in 50 mM KCl; but, at both ionic strengths, BrdUrd substitution in the DNA confers enhanced stability on the complex. The demonstration that a specific mammalian regulatory protein has an enhanced affinity for BrdUrd-substituted DNA further strengthens the possibility that BrdUrd modulates gene expression through an altered binding of regulatory proteins.