Karchner Sibel I, Franks Diana G, Powell Wade H, Hahn Mark E
Biology Department, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA.
J Biol Chem. 2002 Mar 1;277(9):6949-59. doi: 10.1074/jbc.M110779200. Epub 2001 Dec 12.
The effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and related compounds occur via the aryl hydrocarbon receptor (AHR), a member of the basic helix-loop-helix-Per-ARNT-Sim homology (bHLH-PAS) protein superfamily. A single AHR gene has been identified in mammals, whereas many fish species, including the Atlantic killifish (Fundulus heteroclitus) possess two distinct AHR genes (AHR1 and a novel form, AHR2). A mouse bHLH-PAS protein closely related to AHR and designated AHR repressor (AHRR) is induced by 3-methylcholanthrene and represses the transcriptional activity of the AHR. To determine whether AHRR is the mammalian ortholog of fish AHR2 and to investigate the mechanisms by which AHRR regulates AHR function, we cloned an AHRR ortholog in F. heteroclitus with high sequence identity to the mouse and human AHRRs. Killifish AHRR encodes a 680-residue protein with a predicted molecular mass of 75.2 kDa. We show that in vitro expressed AHRR proteins from human, mouse, and killifish all fail to bind [(3)H]TCDD or [(3)H]beta-naphthoflavone. In transient transfection experiments using a luciferase reporter gene under control of AHR response elements, killifish AHRR inhibited the TCDD-dependent transactivation function of both AHR1 and AHR2. AHRR mRNA is widely expressed in killifish tissues and is inducible by TCDD or polychlorinated biphenyls, but its expression is not altered in a population of fish exhibiting genetic resistance to these compounds. The F. heteroclitus AHRR promoter contains three putative AHR response elements. Both AHR1 and AHR2 activated transcription of luciferase driven by the AHRR promoter, and AHRR could repress its own promoter. Thus, AHRR is an evolutionarily conserved, TCDD-inducible repressor of AHR1 and AHR2 function. Phylogenetic analysis shows that AHRR, AHR1, and AHR2 are distinct genes, members of an AHR gene family; these three vertebrate AHR-like genes descended from a single invertebrate AHR.
2,3,7,8-四氯二苯并对二恶英(TCDD)及相关化合物的作用是通过芳烃受体(AHR)介导的,AHR是碱性螺旋-环-螺旋-Per-ARNT-Sim同源性(bHLH-PAS)蛋白超家族的成员。在哺乳动物中已鉴定出单一的AHR基因,而许多鱼类,包括大西洋鳉鱼(Fundulus heteroclitus),拥有两个不同的AHR基因(AHR1和一种新形式AHR2)。一种与AHR密切相关的小鼠bHLH-PAS蛋白,被命名为AHR阻遏物(AHRR),可被3-甲基胆蒽诱导,并抑制AHR的转录活性。为了确定AHRR是否是鱼类AHR2的哺乳动物直系同源物,并研究AHRR调节AHR功能的机制,我们在异齿鳉鱼中克隆了一个与小鼠和人类AHRR具有高度序列同一性的AHRR直系同源物。鳉鱼AHRR编码一种680个氨基酸残基的蛋白质,预测分子量为75.2 kDa。我们发现,人、小鼠和鳉鱼体外表达的AHRR蛋白均不能结合[³H]TCDD或[³H]β-萘黄酮。在使用受AHR反应元件控制的荧光素酶报告基因的瞬时转染实验中,鳉鱼AHRR抑制了AHR1和AHR2的TCDD依赖性反式激活功能。AHRR mRNA在鳉鱼组织中广泛表达,可被TCDD或多氯联苯诱导,但其表达在对这些化合物具有遗传抗性的鱼群中未发生改变。异齿鳉鱼AHRR启动子包含三个假定的AHR反应元件。AHR1和AHR2均激活由AHRR启动子驱动的荧光素酶转录,并且AHRR可以抑制其自身的启动子。因此,AHRR是AHR1和AHR2功能的一种进化保守的、TCDD可诱导的阻遏物。系统发育分析表明,AHRR、AHR1和AHR2是不同的基因,属于AHR基因家族的成员;这三个脊椎动物AHR样基因起源于单个无脊椎动物AHR。