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雌激素受体基因调控机制的多样性。

Diversity in the mechanisms of gene regulation by estrogen receptors.

作者信息

Sanchez Rocio, Nguyen Denis, Rocha Walter, White John H, Mader Sylvie

机构信息

Département de Biochimie, Université de Montréal, CP 6128 Succursale Centre Ville, Montréal, Quebec H3C 3J7, Canada.

出版信息

Bioessays. 2002 Mar;24(3):244-54. doi: 10.1002/bies.10066.

Abstract

The sequencing of the human genome has opened the way for using bioinformatics to identify sets of genes controlled by specific regulatory signals. Here, we review the unexpected diversity of DNA response elements mediating transcriptional regulation by estrogen receptors (ERs), which control the broad physiological effects of estrogens. Consensus palindromic estrogen response elements are found in only a few known estrogen target genes, whereas most responsive genes contain only low-affinity half palindromes, which may also control regulation by other nuclear receptors. ERs can also regulate gene expression in the absence of direct interaction with DNA, via protein-protein interactions with other transcription factors or by modulating the activity of upstream signaling components, thereby significantly expanding the repertoire of estrogen-responsive genes. These diverse mechanisms of action must be taken into account in screening for potential estrogen-responsive sequences in the genome or in regulatory regions of target genes identified by expression profiling.

摘要

人类基因组测序为利用生物信息学识别由特定调控信号控制的基因集开辟了道路。在此,我们综述了介导雌激素受体(ERs)转录调控的DNA反应元件出人意料的多样性,雌激素受体控制着雌激素广泛的生理效应。仅在少数已知的雌激素靶基因中发现了共有回文雌激素反应元件,而大多数反应性基因仅含有低亲和力的半回文序列,这些序列也可能控制其他核受体的调控。ERs还可以在不与DNA直接相互作用的情况下,通过与其他转录因子的蛋白质-蛋白质相互作用或调节上游信号成分的活性来调控基因表达,从而显著扩大雌激素反应性基因的范围。在筛选基因组中潜在的雌激素反应序列或通过表达谱鉴定的靶基因调控区域时,必须考虑这些多样的作用机制。

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