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甲状腺激素反应元件半位点组织及其对甲状腺激素介导转录的影响。

Thyroid hormone response element half-site organization and its effect on thyroid hormone mediated transcription.

作者信息

Paquette Martin A, Atlas Ella, Wade Mike G, Yauk Carole L

机构信息

Environmental Health Science and Research Bureau, Healthy Environments and Consumer Safety Branch, Health Canada, Ottawa, Ontario, Canada; Department of Biology, Carleton University, Ottawa, Ontario, Canada.

Environmental Health Science and Research Bureau, Healthy Environments and Consumer Safety Branch, Health Canada, Ottawa, Ontario, Canada.

出版信息

PLoS One. 2014 Jun 27;9(6):e101155. doi: 10.1371/journal.pone.0101155. eCollection 2014.

Abstract

Thyroid hormone (TH) exerts its effects by binding to the thyroid hormone receptor (TR), which binds to TH response elements (TREs) to regulate target gene expression. We investigated the relative ability of liganded homodimers TR and retinoid X receptor (RXR), and the heterodimer TR/RXR, to regulate gene expression for the TRE half-site organizations: direct repeat 4 (DR4), inverted repeat 0 (IR0) and everted repeat 6 (ER6). Luciferase reporter assays using a DR4 TRE suggest that both the TR homodimer and TR/RXR heterodimer regulate luciferase expression in the presence of their respective ligands. However, in the presence of the IR0 TRE, transfection with TR/RXR and RXR alone increased luciferase activity and there was no effect of TR alone. The presence of 9-cis-retinoic acid was necessary for luciferase expression, whereas TH treatment alone was insufficient. For the ER6 TRE, transfection with TR/RXR, TR alone and RXR alone (in the presence of their respective ligands) all caused a significant increase in luciferase activity. When both ligands were present, transfection with both TR/RXR caused more activation. Finally, we investigated the efficacy of the TR-antagonist 1-850 in inhibiting transcription by TR or TR/RXR at DR4 and ER6 TREs. We found that 1-850 did not suppress luciferase activation in the presence of TR/RXR for the ER6 TRE, suggesting conformational changes of the ligand binding domain of the TR when bound to different TRE half-site organizations. Collectively, the findings indicate that there are fundamental differences between TRE configurations that affect nuclear receptor interactions with the response element and ability to bind ligands and antagonists.

摘要

甲状腺激素(TH)通过与甲状腺激素受体(TR)结合发挥作用,TR与甲状腺激素反应元件(TREs)结合以调节靶基因表达。我们研究了配体化的同源二聚体TR和视黄酸X受体(RXR)以及异源二聚体TR/RXR对TRE半位点组织(直接重复序列4(DR4)、反向重复序列0(IR0)和外翻重复序列6(ER6))基因表达的调节能力。使用DR4 TRE的荧光素酶报告基因检测表明,TR同源二聚体和TR/RXR异源二聚体在各自配体存在的情况下均调节荧光素酶表达。然而,在IR0 TRE存在的情况下,单独转染TR/RXR和RXR可增加荧光素酶活性,而单独的TR则无作用。9-顺式视黄酸的存在是荧光素酶表达所必需的,而单独的TH处理则不足。对于ER6 TRE,单独转染TR/RXR、TR和RXR(在各自配体存在的情况下)均导致荧光素酶活性显著增加。当两种配体都存在时,同时转染TR/RXR会引起更多的激活。最后,我们研究了TR拮抗剂1-850在DR4和ER6 TRE处抑制TR或TR/RXR转录的功效。我们发现,对于ER6 TRE,在存在TR/RXR的情况下,1-850不会抑制荧光素酶激活,这表明当TR与不同的TRE半位点组织结合时,其配体结合域会发生构象变化。总体而言,这些发现表明,TRE构型之间存在根本差异,这些差异会影响核受体与反应元件的相互作用以及结合配体和拮抗剂的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cdd/4074170/8fbf4b9e3e09/pone.0101155.g001.jpg

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