首页> 外文期刊>Aquatic Toxicology >New cytochrome P450 1B1, 1C2 and 1D1 genes in the killifish Fundulus heteroclitus: Basal expression and response of five killifish CYP1s to the AHR agonist PCB126
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New cytochrome P450 1B1, 1C2 and 1D1 genes in the killifish Fundulus heteroclitus: Basal expression and response of five killifish CYP1s to the AHR agonist PCB126

机译:介壳鱼类异体cli中的新细胞色素P450 1B1、1C2和1D1基因:五个介壳鱼类CYP1对AHR激动剂PCB126的基础表达和应答

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摘要

Knowledge of the complement of cytochrome P450 (CYP) genes is essential to understanding detoxification and bioactivation mechanisms for organic contaminants. We cloned three new CYP1 genes, CYP1B1, CYP1C2 and CYP1D1, from the killifish Fundulus heteroclitus, an important model in environmental toxicology. Expression of the new CYP1s along with previously known CYP1A and CYP1C1 was measured by qPCR in eight different organs. Organ distribution was similar for the two CYP1Cs, but otherwise patterns and extent of expression differed among the genes. The AHR agonist 3,3',4,4',5-pentachlorobiphenyl (PCB126) (31pmol/g fish) induced expression of CYP1A and CYP1B1 in all organs examined, while CYP1C1 was induced in all organs except testis. The largest changes in response to PCB126 were induction of CYP1A in testis (~700-fold) and induction of CYP1C1 in liver (~500-fold). CYP1B1 in liver and gut, CYP1A in brain and CYP1C1 in gill also were induced strongly by PCB126 (>100-fold). CYP1C1 expression levels were higher than CYP1C2 in almost all tissues and CYP1C2 was much less responsive to PCB126. In contrast to the other genes, CYP1D1 was not induced by PCB126 in any of the organs. The organ-specific response of CYP1s to PCB126 implies differential involvement in effects of halogenated aromatic hydrocarbons in different organs. The suite of inducible CYP1s could enhance the use of F. heteroclitus in assessing aquatic contamination by AHR agonists. Determining basal and induced levels of protein and the substrate specificity for all five CYP1s will be necessary to better understand their roles in chemical effects and physiology.
机译:了解细胞色素P450(CYP)基因的补体对于理解有机污染物的解毒和生物激活机制至关重要。我们从环境毒理学中的一个重要模型即kill鱼眼底中克隆了三个新的CYP1基因CYP1B1,CYP1C2和CYP1D1。通过qPCR测量了八个不同器官中新CYP1s与先前已知的CYP1A和CYP1C1的表达。两个CYP1Cs的器官分布相似,但其他基因之间的表达方式和表达程度不同。 AHR激动剂3,3',4,4',5-五氯联苯(PCB126)(31 pmol/g鱼)诱导所有受检器官中CYP1A和CYP1B1的表达,而CYP1C1在除睾丸外的所有器官中均被诱导。对PCB126的响应变化最大的是睾丸中CYP1A的诱导(约700倍)和肝脏中CYP1C1的诱导(约500倍)。肝和肠中的CYP1B1,脑中的CYP1A和g中的CYP1C1也被PCB126强烈诱导(> 100倍)。在几乎所有组织中,CYP1C1的表达水平均高于CYP1C2,而CYP1C2对PCB126的响应则低得多。与其他基因相反,CYP1D1没有在任何器官中被PCB126诱导。 CYP1s对PCB126的器官特异性反应意味着在不同器官中对卤代芳烃的影响存在差异。这套可诱导的CYP1s可能会增强异形镰刀菌在评估AHR激动剂对水生生物的污染中的用途。确定所有五个CYP1的蛋白质的基础和诱导水平以及底物特异性对于更好地了解其在化学作用和生理学中的作用将是必要的。

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