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新型CYP2A13转基因小鼠模型的构建与鉴定

Generation and characterization of a novel CYP2A13--transgenic mouse model.

作者信息

Jia Kunzhi, Li Lei, Liu Zhihua, Hartog Matthew, Kluetzman Kerri, Zhang Qing-Yu, Ding Xinxin

机构信息

Wadsworth Center, New York State Department of Health, and School of Public Health, State University of New York, Albany, New York.

Wadsworth Center, New York State Department of Health, and School of Public Health, State University of New York, Albany, New York

出版信息

Drug Metab Dispos. 2014 Aug;42(8):1341-8. doi: 10.1124/dmd.114.059188. Epub 2014 Jun 6.

Abstract

CYP2A13, CYP2B6, and CYP2F1 are neighboring cytochrome P450 genes on human chromosome 19, and the enzymes that they encode overlap in substrate specificity. A CYP2A13/2B6/2F1-transgenic mouse, in which CYP2A13 and 2F1 are both expressed in the respiratory tract and CYP2B6 is expressed in the liver, was recently generated. We generated a CYP2A13 (only) transgenic mouse so that the specific activity of CYP2A13 can be determined. The CYP2B6 and CYP2F1 genes in the CYP2A13/2B6/2F1 genomic clone were inactivated via genetic manipulations, and CYP2A13 was kept intact. A CYP2A13 (only) transgenic (2A13-TG) mouse was generated using the engineered construct and then characterized to confirm transgene integrity and determine copy numbers. The 2A13-TG mice were normal in gross morphology, development, and fertility. As in the CYP2A13/2B6/2F1-transgenic mouse, CYP2A13 expression in the 2A13-TG mouse was limited to the respiratory tract; in contrast, CYP2B6 and 2F1 proteins were not detected. Additional studies using the CYP2A13-humanized (2A13-TG/Cyp2abfgs-null) mouse produced by intercrossing between 2A13-TG and Cyp2abfgs-null mice confirmed that the transgenic CYP2A13 is active in the bioactivation of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), a lung procarcinogen. The 2A13-TG mouse should be valuable for assessing specific roles of human CYP2A13 in xenobiotic toxicity in the respiratory tract.

摘要

CYP2A13、CYP2B6和CYP2F1是人类19号染色体上相邻的细胞色素P450基因,它们所编码的酶在底物特异性方面存在重叠。最近培育出了一种CYP2A13/2B6/2F1转基因小鼠,其中CYP2A13和2F1在呼吸道中均有表达,而CYP2B6在肝脏中表达。我们培育了一种仅表达CYP2A13的转基因小鼠,以便能够测定CYP2A13的比活性。通过基因操作使CYP2A13/2B6/2F1基因组克隆中的CYP2B6和CYP2F1基因失活,而CYP2A13保持完整。使用构建好的载体培育出了仅表达CYP2A13的转基因(2A13-TG)小鼠,然后对其进行特征分析以确认转基因的完整性并确定拷贝数。2A13-TG小鼠在大体形态、发育和生育能力方面均正常。与CYP2A13/2B6/2F1转基因小鼠一样,2A13-TG小鼠中CYP2A13的表达仅限于呼吸道;相反,未检测到CYP2B6和2F1蛋白。使用通过将2A13-TG小鼠与Cyp2abfgs基因敲除小鼠杂交产生的CYP2A13人源化(2A13-TG/Cyp2abfgs基因敲除)小鼠进行的进一步研究证实,转基因CYP2A13在肺致癌物4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)的生物活化中具有活性。2A13-TG小鼠对于评估人类CYP2A13在呼吸道中异源物质毒性的特定作用应该具有重要价值。

相似文献

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Generation and characterization of a novel CYP2A13--transgenic mouse model.新型CYP2A13转基因小鼠模型的构建与鉴定
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