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在小鼠肝脏中进行 PXR 顺式调控元件的 ChIP 实验。

ChIPing the cistrome of PXR in mouse liver.

机构信息

Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA.

出版信息

Nucleic Acids Res. 2010 Dec;38(22):7943-63. doi: 10.1093/nar/gkq654. Epub 2010 Aug 6.

Abstract

The pregnane X receptor (PXR) is a key regulator of xenobiotic metabolism and disposition in liver. However, little is known about the PXR DNA-binding signatures in vivo, or how PXR regulates novel direct targets on a genome-wide scale. Therefore, we generated a roadmap of hepatic PXR bindings in the entire mouse genome [chromatin immunoprecipitation (ChIP)-Seq]. The most frequent PXR DNA-binding motif is the AGTTCA-like direct repeat with a 4 bp spacer [direct repeat (DR)-4)]. Surprisingly, there are also high motif occurrences with spacers of a periodicity of 5 bp, forming a novel DR-(5 n+4) pattern for PXR binding. PXR-binding overlaps with the epigenetic mark for gene activation (histone-H3K4-di-methylation), but not with epigenetic marks for gene suppression (DNA methylation or histone-H3K27-tri-methylation) (ChIP-on-chip). After administering a PXR agonist, changes in mRNA of most PXR-direct target genes correlate with increased PXR binding. Specifically, increased PXR binding triggers the trans-activation of critical drug-metabolizing enzymes and transporters. The mRNA induction of these genes is absent in PXR-null mice. The current work provides the first in vivo evidence of PXR DNA-binding signatures in the mouse genome, paving the path for predicting and further understanding the multifaceted roles of PXR in liver.

摘要

妊娠相关 X 受体 (PXR) 是肝脏中外源物质代谢和处置的关键调节因子。然而,目前对于 PXR 在体内的 DNA 结合特征,以及 PXR 如何在全基因组范围内调控新的直接靶标知之甚少。因此,我们生成了整个小鼠基因组中 PXR 结合的路线图[染色质免疫沉淀 (ChIP)-Seq]。最常见的 PXR DNA 结合基序是具有 4 个碱基间隔的 AGTTCA 样直接重复[直接重复 (DR)-4)]。令人惊讶的是,也存在具有周期性 5 个碱基间隔的高 motif 出现,形成了 PXR 结合的新型 DR-(5 n+4)模式。PXR 结合与基因激活的表观遗传标记(组蛋白 H3K4-二甲基化)重叠,但与基因抑制的表观遗传标记(DNA 甲基化或组蛋白 H3K27-三甲基化)不重叠(ChIP-on-chip)。在给予 PXR 激动剂后,大多数 PXR 直接靶基因的 mRNA 变化与 PXR 结合增加相关。具体而言,PXR 结合的增加触发了关键药物代谢酶和转运体的反式激活。这些基因的 mRNA 诱导在 PXR 缺失小鼠中不存在。目前的工作为小鼠基因组中 PXR DNA 结合特征提供了第一个体内证据,为预测和进一步理解 PXR 在肝脏中的多方面作用铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e126/3001051/f27d4ea61e13/gkq654f1.jpg

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