整合核受体迁移的基因调控模型。

Nuclear receptor signaling Pub Date : 2006-01-01 Epub Date: 2006-04-28 DOI:10.1621/nrs.04010
Laurent Gelman, Jerome N Feige, Cicerone Tudor, Yves Engelborghs, Walter Wahli, Beatrice Desvergne
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引用次数: 12

摘要

核受体在活细胞中的作用模式是一个积极研究的领域,但由于缺乏能够评估体内分子机制的方法,直到最近,许多仍然是假设的。然而,近年来,荧光显微镜方法的发展使得对活细胞或生物体中核受体直接调控基因的分子机制的解剖成为可能。在我们对活细胞中过氧化物酶体增殖物激活受体(ppar)的分析之后,我们在这里讨论了使用这些工具产生的不同模型,这些模型试图将移动性、DNA结合或染色质相互作用和转录活性联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Integrating nuclear receptor mobility in models of gene regulation.

Integrating nuclear receptor mobility in models of gene regulation.

Integrating nuclear receptor mobility in models of gene regulation.

The mode of action of nuclear receptors in living cells is an actively investigated field but much remains hypothetical due to the lack, until recently, of methods allowing the assessment of molecular mechanisms in vivo. However, these last years, the development of fluorescence microscopy methods has allowed initiating the dissection of the molecular mechanisms underlying gene regulation by nuclear receptors directly in living cells or organisms. Following our analyses on peroxisome proliferator activated receptors (PPARs) in living cells, we discuss here the different models arising from the use of these tools, that attempt to link mobility, DNA binding or chromatin interaction, and transcriptional activity.

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