Biology Department, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA; Departamento de Bioquímica, CCB, Universidade Federal de Santa Catarina, Florianópolis, SC 88040-900, Brazil.
Aquat Toxicol. 2013 Oct 15;142-143:447-57. doi: 10.1016/j.aquatox.2013.09.014. Epub 2013 Sep 20.
The pregnane X receptor (PXR) (nuclear receptor NR1I2) is a ligand activated transcription factor, mediating responses to diverse xenobiotic and endogenous chemicals. The properties of PXR in fish are not fully understood. Here we report on cloning and characterization of full-length PXR of zebrafish, Danio rerio, and pxr expression in vivo. Initial efforts gave a cDNA encoding a 430 amino acid protein identified as zebrafish pxr by phylogenetic and synteny analysis. The sequence of the cloned Pxr DNA binding domain (DBD) was highly conserved, with 74% identity to human PXR-DBD, while the ligand-binding domain (LBD) of the cloned sequence was only 44% identical to human PXR-LBD. Sequence variation among clones in the initial effort prompted sequencing of multiple clones from a single fish. There were two prominent variants, one sequence with S183, Y218 and H383 and the other with I183, C218 and N383, which we designate as alleles pxr1 (nr1i21) and pxr2 (nr1i22), respectively. In COS-7 cells co-transfected with a PXR-responsive reporter gene, the full-length Pxr1 (the more common variant) was activated by known PXR agonists clotrimazole and pregnenolone 16α-carbonitrile but to a lesser extent than the full-length human PXR. Activation of full-length Pxr1 was only 10% of that with the Pxr*1 LBD. Quantitative real time PCR analysis showed prominent expression of pxr in liver and eye, as well as brain and intestine of adult zebrafish. The pxr was expressed in heart and kidney at levels similar to that in intestine. The expression of pxr in liver was weakly induced by ligands for mammalian PXR or constitutive androstane receptor (NR1I3). The results establish a foundation for PXR studies in this vertebrate model. PXR allelic variation and the differences between the full-length PXR and the LBD in reporter assays have implications for assessing the action of PXR ligands in zebrafish.
pregnane X 受体 (PXR) (核受体 NR1I2) 是一种配体激活的转录因子,介导对各种外源和内源性化学物质的反应。鱼类 PXR 的特性尚未完全了解。在这里,我们报道了斑马鱼 Danio rerio 的全长 PXR 的克隆和特性,并在体内研究了 pxr 的表达。最初的努力得到了一个编码 430 个氨基酸的蛋白质的 cDNA,通过系统发育和基因同线性分析将其鉴定为斑马鱼 pxr。克隆的 Pxr DNA 结合域 (DBD) 序列高度保守,与人 PXR-DBD 的同一性为 74%,而克隆序列的配体结合域 (LBD) 与人 PXR-LBD 的同一性仅为 44%。最初努力中克隆之间的序列变异促使我们从一条鱼中测序多个克隆。有两个主要的变体,一个序列为 S183、Y218 和 H383,另一个序列为 I183、C218 和 N383,我们分别将其命名为等位基因 pxr1(nr1i21)和 pxr2(nr1i22)。在与 PXR 反应性报告基因共转染的 COS-7 细胞中,全长 Pxr1(更常见的变体)被已知的 PXR 激动剂克霉唑和孕烯醇酮 16α-氰化物激活,但激活程度低于全长人 PXR。全长 Pxr1 的激活仅为全长 Pxr*1 LBD 的 10%。定量实时 PCR 分析显示,成年斑马鱼的肝脏和眼睛以及大脑和肠道中明显表达 pxr。心脏和肾脏中的 pxr 表达水平与肠道相似。配体对哺乳动物 PXR 或组成型雄激素受体 (NR1I3) 的诱导作用使肝脏中 pxr 的表达较弱。该结果为该脊椎动物模型中的 PXR 研究奠定了基础。PXR 等位基因变异以及报告基因检测中全长 PXR 和 LBD 之间的差异,对评估 PXR 配体在斑马鱼中的作用具有重要意义。