Effects of gamma irradiation on the DNA-protein complex between the estrogen response element and the estrogen receptor

被引:1
作者
Stisova, Viktorie [1 ]
Goffinont, Stephane [2 ]
Spotheim-Maurizot, Melanie [2 ]
Davidkova, Marie [1 ]
机构
[1] Nucl Phys Inst AS CR, Radiat Dosimetry Dept, Prague 18086 8, Czech Republic
[2] CNRS, Ctr Biophys Mol, F-45071 Orleans 2, France
关键词
DNA-protein complex; Estrogen response element; Estrogen receptor; Ionizing radiation; BINDING DOMAIN; BREAST-CANCER; TRANSCRIPTIONAL ACTIVATION; RADIATION-DAMAGE; HORMONE-BINDING; TAMOXIFEN; BETA; RADIOLYSIS; ALPHA; CELLS;
D O I
10.1016/j.radphyschem.2010.03.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Signaling by estrogens, risk factors in breast cancer, is mediated through their binding to the estrogen receptor protein (ER), followed by the formation of a complex between ER and a DNA sequence, called estrogen response element (ERE). Anti-estrogens act as competitive inhibitors by blocking the signal transduction. We have studied in vitro the radiosensitivity of the complex between ER alpha, a subtype of this receptor, and a DNA fragment bearing ERE, as well as the influence of an estrogen (estradiol) or an anti-estrogen (tamoxifen) on this radiosensitivity. We observe that the complex is destabilized upon irradiation with gamma rays in aerated aqueous solution. The analysis of the decrease of binding abilities of the two partners shows that destabilization is mainly due to the damage to the protein. The destabilization is reduced when irradiating in presence of tamoxifen and is increased in presence of estradiol. These effects are due to opposite influences of the ligands on the loss of binding ability of ER. The mechanism that can account for our results is: binding of estradiol or tamoxifen induces distinct structural changes of the ER ligand-binding domain that can trigger (by allostery) distinct structural changes of the ER DNA-binding domains and thus, can differently affect ER-ERE interaction. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:880 / 889
页数:10
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