Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Nucleic Acids Res. 2010 Dec;38(22):7943-63. doi: 10.1093/nar/gkq654. Epub 2010 Aug 6.
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.
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。