Molecular cloning and characterization of three novel cytochrome P450 2D isoforms, CYP2D20, CYP2D27, and CYP2D28 in the Syrian hamster (Mesocricetus auratus)

Tomohiro Oka , Morio Fukuhara , Fusao Ushio , Kouichi Kurose
{"title":"Molecular cloning and characterization of three novel cytochrome P450 2D isoforms, CYP2D20, CYP2D27, and CYP2D28 in the Syrian hamster (Mesocricetus auratus)","authors":"Tomohiro Oka ,&nbsp;Morio Fukuhara ,&nbsp;Fusao Ushio ,&nbsp;Kouichi Kurose","doi":"10.1016/S0742-8413(00)00142-0","DOIUrl":null,"url":null,"abstract":"<div><p>We cloned three novel cytochrome P450 (CYP) 2D cDNAs in the Syrian hamster (<em>Mesocricetus auratus</em>). Each clone contained an open reading frame of 1500 nucleotides encoding a protein of 500 amino acids. The deduced amino acid sequences of these had high identities with those of the other CYP2D members, therefore, the clones were assigned as CYP2D20, CYP2D27, and CYP2D28. Northern blot analysis showed that the CYP2D27 mRNA was expressed in liver, but not in kidney, small intestine, and brain, while the CYP2D20 and CYP2D28 mRNAs were not detected in these tissues examined. The expression of CYP2D27 mRNA in liver did not show sex difference and was not induced by either 3-methylcholanthrene or phenobarbital treatment. We characterized the enzyme activities of recombinant CYP2D27 expressed in COS-7 cells. The CYP2D27 protein had the bufuralol 1′-hydroxylase and debrisoquine 4-hydroxylase activities that are specific to the CYP2D subfamily.</p></div>","PeriodicalId":10586,"journal":{"name":"Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2000-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0742-8413(00)00142-0","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0742841300001420","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

We cloned three novel cytochrome P450 (CYP) 2D cDNAs in the Syrian hamster (Mesocricetus auratus). Each clone contained an open reading frame of 1500 nucleotides encoding a protein of 500 amino acids. The deduced amino acid sequences of these had high identities with those of the other CYP2D members, therefore, the clones were assigned as CYP2D20, CYP2D27, and CYP2D28. Northern blot analysis showed that the CYP2D27 mRNA was expressed in liver, but not in kidney, small intestine, and brain, while the CYP2D20 and CYP2D28 mRNAs were not detected in these tissues examined. The expression of CYP2D27 mRNA in liver did not show sex difference and was not induced by either 3-methylcholanthrene or phenobarbital treatment. We characterized the enzyme activities of recombinant CYP2D27 expressed in COS-7 cells. The CYP2D27 protein had the bufuralol 1′-hydroxylase and debrisoquine 4-hydroxylase activities that are specific to the CYP2D subfamily.

叙利亚仓鼠细胞色素P450 2D新异构体CYP2D20、CYP2D27和CYP2D28的分子克隆与鉴定
我们在叙利亚仓鼠(Mesocricetus auratus)中克隆了三个新的细胞色素P450 (CYP) 2D cdna。每个克隆包含1500个核苷酸的开放阅读框,编码500个氨基酸的蛋白质。这些克隆的氨基酸序列与其他CYP2D成员的氨基酸序列具有较高的一致性,因此,这些克隆被命名为CYP2D20、CYP2D27和CYP2D28。Northern blot分析显示,CYP2D27 mRNA在肝脏中表达,而在肾脏、小肠和脑中不表达,而CYP2D20和CYP2D28 mRNA在这些组织中未检测到。肝脏中CYP2D27 mRNA的表达不存在性别差异,3-甲基胆蒽和苯巴比妥均未诱导CYP2D27 mRNA表达。我们鉴定了重组CYP2D27在COS-7细胞中表达的酶活性。CYP2D27蛋白具有特定于CYP2D亚家族的丁醛醇1′-羟化酶和碎片醌4-羟化酶活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信