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Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 in Cynomolgus Macaques
Cytochromes P450 (P450) are important for not only drug metabolism and toxicity, but also biosynthesis and metabolism of cholesterol and bile acids, and steroid synthesis. In cynomolgus macaques, widely used in biomedical research, we have characterized P450 cDNAs, which were isolated as expressed s...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Veterinary Science
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300383/ https://www.ncbi.nlm.nih.gov/pubmed/25649950 http://dx.doi.org/10.1292/jvms.14-0313 |
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author | UNO, Yasuhiro HOSAKA, Shinya YAMAZAKI, Hiroshi |
author_facet | UNO, Yasuhiro HOSAKA, Shinya YAMAZAKI, Hiroshi |
author_sort | UNO, Yasuhiro |
collection | PubMed |
description | Cytochromes P450 (P450) are important for not only drug metabolism and toxicity, but also biosynthesis and metabolism of cholesterol and bile acids, and steroid synthesis. In cynomolgus macaques, widely used in biomedical research, we have characterized P450 cDNAs, which were isolated as expressed sequence tags of cynomolgus macaque liver. In this study, cynomolgus CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 cDNAs were characterized by sequence analysis, phylogenetic analysis and tissue expression pattern. By sequence analysis, these five cynomolgus P450s had high sequence identities (94–99%) to the human orthologs in amino acids. By phylogenetic analysis, each cynomolgus P450 was more closely related to the human ortholog as compared with the dog or rat ortholog. By quantitative polymerase chain reaction, among the 10 tissue types, CYP7A1 and CYP17A1 mRNAs were preferentially expressed in liver and adrenal gland, respectively. Cynomolgus CYP27A1 and CYP51A1 mRNAs were most abundantly expressed in liver and testis, respectively. Cynomolgus CYP20A1 mRNA was expressed in all the tissues, including brain and liver. Tissue expression patterns of each cynomolgus P450 were generally similar to that of the human ortholog. These results suggest the molecular similarities of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 between cynomolgus macaques and humans. |
format | Online Article Text |
id | pubmed-4300383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43003832015-02-06 Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 in Cynomolgus Macaques UNO, Yasuhiro HOSAKA, Shinya YAMAZAKI, Hiroshi J Vet Med Sci Pharmacology Cytochromes P450 (P450) are important for not only drug metabolism and toxicity, but also biosynthesis and metabolism of cholesterol and bile acids, and steroid synthesis. In cynomolgus macaques, widely used in biomedical research, we have characterized P450 cDNAs, which were isolated as expressed sequence tags of cynomolgus macaque liver. In this study, cynomolgus CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 cDNAs were characterized by sequence analysis, phylogenetic analysis and tissue expression pattern. By sequence analysis, these five cynomolgus P450s had high sequence identities (94–99%) to the human orthologs in amino acids. By phylogenetic analysis, each cynomolgus P450 was more closely related to the human ortholog as compared with the dog or rat ortholog. By quantitative polymerase chain reaction, among the 10 tissue types, CYP7A1 and CYP17A1 mRNAs were preferentially expressed in liver and adrenal gland, respectively. Cynomolgus CYP27A1 and CYP51A1 mRNAs were most abundantly expressed in liver and testis, respectively. Cynomolgus CYP20A1 mRNA was expressed in all the tissues, including brain and liver. Tissue expression patterns of each cynomolgus P450 were generally similar to that of the human ortholog. These results suggest the molecular similarities of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 between cynomolgus macaques and humans. The Japanese Society of Veterinary Science 2014-09-03 2014-12 /pmc/articles/PMC4300383/ /pubmed/25649950 http://dx.doi.org/10.1292/jvms.14-0313 Text en ©2014 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Pharmacology UNO, Yasuhiro HOSAKA, Shinya YAMAZAKI, Hiroshi Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 in Cynomolgus Macaques |
title | Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1
in Cynomolgus Macaques |
title_full | Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1
in Cynomolgus Macaques |
title_fullStr | Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1
in Cynomolgus Macaques |
title_full_unstemmed | Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1
in Cynomolgus Macaques |
title_short | Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1
in Cynomolgus Macaques |
title_sort | identification and analysis of cyp7a1, cyp17a1, cyp20a1, cyp27a1 and cyp51a1
in cynomolgus macaques |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300383/ https://www.ncbi.nlm.nih.gov/pubmed/25649950 http://dx.doi.org/10.1292/jvms.14-0313 |
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