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将核受体流动性整合到基因调控模型中。

Integrating nuclear receptor mobility in models of gene regulation.

作者信息

Gelman Laurent, Feige Jerome N, Tudor Cicerone, Engelborghs Yves, Wahli Walter, Desvergne Beatrice

机构信息

Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.

出版信息

Nucl Recept Signal. 2006;4:e010. doi: 10.1621/nrs.04010. Epub 2006 Apr 28.

Abstract

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.

摘要

核受体在活细胞中的作用模式是一个正在积极研究的领域,但由于直到最近仍缺乏能够在体内评估分子机制的方法,许多方面仍属假说。然而,在过去几年中,荧光显微镜方法的发展使得能够直接在活细胞或生物体中开始剖析核受体介导的基因调控的分子机制。在对活细胞中的过氧化物酶体增殖物激活受体(PPARs)进行分析之后,我们在此讨论使用这些工具产生的不同模型,这些模型试图将流动性、DNA结合或染色质相互作用与转录活性联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee0/1472671/4fe0186571bd/nrs04010.f1.jpg

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