干扰雌激素受体调控的转录动力学。

S A Johnsen, S Kangaspeska, G Reid, F Gannon
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引用次数: 8

摘要

近年来,越来越多的人认识到转录因子激活基因的静态二维模型是不够的。基于一些小组的工作(Kang et al. 2002;Liu and Bagchi 2004;Metivier等人,2003;Park et al. 2005;Reid et al. 2003;Shang et al. 2000;Sharma and Fondell 2002;Vaisanen et al. 2005),越来越清楚的是,核受体的转录调控是一个动态和周期性的过程(Metivier et al. 2006)。这种认识的转变产生了重大的后果,从核受体作为配体激活因子与反应元件结合以激活靶基因的表达,到受体反复结合以实现转录的过程。本章概述了将激活过程视为周期性过程所产生的新见解,以及开发调节雌激素受体活性的新策略的后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interfering with the dynamics of estrogen receptor-regulated transcription.

In recent years, there has been a growing realization that a static two-dimensional model of gene activation by transcription factors is inadequate. Based on the work from a number of groups (Kang et al. 2002; Liu and Bagchi 2004; Metivier et al. 2003; Park et al. 2005; Reid et al. 2003; Shang et al. 2000; Sharma and Fondell 2002; Vaisanen et al. 2005), it is becoming clear that transcriptional regulation by nuclear receptors is a dynamic and cyclical process (Metivier et al. 2006). There are significant consequences that arise from this shift in understanding, from nuclear receptors as ligand activated factors that bind to a response element to activate expression of a target gene to a process where the receptor repeatedly binds in order to achieve transcription. New insights that arise from viewing the activation process as cyclical and the consequences of this for developing new strategies that modulate the activity of the estrogen receptor are outlined in this chapter.

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