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鸡(Gallus gallus)芳烃受体阻遏物的分子和功能特征:种间相似性和差异。

Molecular and functional characterization of Aryl hydrocarbon receptor repressor from the chicken (Gallus gallus): interspecies similarities and differences.

机构信息

Center for Marine Environmental Studies, Ehime University, Bunkyo-cho 2-5, Matsuyama, Japan.

出版信息

Toxicol Sci. 2011 Feb;119(2):319-34. doi: 10.1093/toxsci/kfq336. Epub 2010 Nov 3.

Abstract

The aryl hydrocarbon receptor (AHR) repressor (AHRR) has been recognized as a negative feedback modulator of AHR-mediated responses in fish and mammals. However, the repressive mechanism by the AHRR has not been investigated in other animals. To understand the molecular mechanism of dioxin toxicity and the evolutionary history of the AHR signaling pathway in avian species, the present study addresses chicken AHRR (ckAHRR). The complementary DNA sequence of ckAHRR encodes an 84-kDa protein sharing 29-52% identities with other AHRRs. High levels of ckAHRR messenger RNA were recorded in the kidney and intestine of nontreated chicks. In hepatoma LMH cells, the 2,3,7, 8-tetrachlorodibenzo-p-dioxin (TCDD) 50% effective concentration value for ckAHRR induction (0.0016nM) was the same as that for chicken cytochrome P450 1A5 (ckCYP1A5), implying a shared transcriptional regulation of ckAHRR and ckCYP1A5 by chicken AHR (ckAHR). In ckAHRR transient transfection assays, ckAHRR repressed both ckAHR1- and ckAHR2-mediated transcriptional activities. Deletion and mutation assays revealed that basic helix-loop-helix/Per-ARNT-Sim A domains of ckAHRR, particularly 217-402 amino acid residues, are indispensable for the repression, but the AHR nuclear translocator sequestration by ckAHRR and SUMOylation of ckAHRR are not involved in its repressive mechanism. Additionally, subcellular localization assay of ckAHR1-enhanced green fluorescent protein fusion protein showed that ckAHRR did not affect nuclear translocation of the ckAHR1. Furthermore, ckAHRR inhibited the TCDD- and 17β estradiol-enhanced ckCYP1A5 transcription through AHR-estrogen receptor α (ERα) cross talk. Taken together, the function of AHRR is conserved in chicken in terms of the negative regulation of AHR and ERα activities, but its functional mechanism is likely distinct from those of the mammalian and fish homologues.

摘要

芳香烃受体 (AHR) 抑制剂 (AHRR) 已被认为是鱼类和哺乳动物中 AHR 介导的反应的负反馈调节剂。然而,AHRR 的抑制机制尚未在其他动物中进行研究。为了了解二恶英毒性的分子机制和禽类 AHR 信号通路的进化历史,本研究探讨了鸡 AHRR(ckAHRR)。ckAHRR 的 cDNA 序列编码一个 84kDa 的蛋白质,与其他 AHRR 具有 29-52%的同源性。未处理雏鸡的肾脏和肠道中记录到 ckAHRR 信使 RNA 的高水平。在肝癌 LMH 细胞中,2,3,7,8-四氯二苯并对二恶英 (TCDD) 诱导 ckAHRR 的 50%有效浓度值(0.0016nM)与鸡细胞色素 P450 1A5(ckCYP1A5)相同,表明鸡 AHR(ckAHR)对 ckAHRR 和 ckCYP1A5 的转录调控具有共享性。在 ckAHRR 瞬时转染实验中,ckAHRR 抑制了 ckAHR1 和 ckAHR2 介导的转录活性。缺失和突变实验表明,ckAHRR 的基本螺旋-环-螺旋/Per-ARNT-Sim A 结构域,特别是 217-402 个氨基酸残基,对于抑制是必不可少的,但 ckAHRR 对 AHR 核易位的阻断和 ckAHRR 的 SUMO 化不参与其抑制机制。此外,ckAHR1-增强型绿色荧光蛋白融合蛋白的亚细胞定位实验表明,ckAHRR 不影响 ckAHR1 的核易位。此外,ckAHRR 通过 AHR-雌激素受体 α(ERα)交叉对话抑制 TCDD 和 17β 雌二醇增强的 ckCYP1A5 转录。总之,AHRR 的功能在鸡中是保守的,表现在对 AHR 和 ERα 活性的负调节,但它的功能机制可能与哺乳动物和鱼类同源物不同。

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