Enhancer elements in the mouse CYP1A2 gene: A comparative sequencing among different inbred mouse strains

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Title: Enhancer elements in the mouse CYP1A2 gene: A comparative sequencing among different inbred mouse strains
Authors: Mikhailova, Olga N.1,2 pharmacogenomics@ngs.ru, Gulyaeva, Lyudmila F.1, Filipenko, Maxim L.2, Kaledin, Vasily I.3
Source: Mutation Research - Genetic Toxicology & Environmental Mutagenesis. Aug2007, Vol. 632 Issue 1/2, p99-103. 5p.
Subject Terms: Cytochrome P-450, Genetic polymorphism research, Laboratory mice, Medical research
Abstract: Abstract: CYP1A2 expression is constitutively high in mouse liver and is well known for metabolizing several drugs and many procarcinogens to reactive intermediates that can cause toxicity or cancer. In the present study, the basal level of hepatic CYP1A2 activity was shown to vary among different inbred mouse strains. The highest methoxyresorufin-O-demethylase activity (261±52pmol/mgprotein/min) was registered in CC57BR and the lowest (82±11pmol/mgprotein/min) in C3H/a. We have tested the hypothesis that possible polymorphisms in regulatory elements in the 5′-upstream region of the mouse CYP1A2 gene could cause the differences in CYP1A2 enzyme activity among different inbred strains. We have performed a study on the CYP1A2 gene by sequencing the regulatory region from −4675 to −4204 where two enhancer elements were recently identified. The absence of mutation prescribing the phenotype in the CYP1A2 gene was found. The region studied seems to be a highly conserved in mice and not to be associated with interstrain differences in constitutive CYP1A2 enzyme activity. [Copyright &y& Elsevier]
Copyright of Mutation Research - Genetic Toxicology & Environmental Mutagenesis is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Enhancer elements in the mouse CYP1A2 gene: A comparative sequencing among different inbred mouse strains
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  Data: <searchLink fieldCode="AR" term="%22Mikhailova%2C+Olga+N%2E%22">Mikhailova, Olga N.</searchLink><relatesTo>1,2</relatesTo><i> pharmacogenomics@ngs.ru</i><br /><searchLink fieldCode="AR" term="%22Gulyaeva%2C+Lyudmila+F%2E%22">Gulyaeva, Lyudmila F.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Filipenko%2C+Maxim+L%2E%22">Filipenko, Maxim L.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Kaledin%2C+Vasily+I%2E%22">Kaledin, Vasily I.</searchLink><relatesTo>3</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22Mutation+Research+-+Genetic+Toxicology+%26+Environmental+Mutagenesis%22">Mutation Research - Genetic Toxicology & Environmental Mutagenesis</searchLink>. Aug2007, Vol. 632 Issue 1/2, p99-103. 5p.
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  Data: <searchLink fieldCode="DE" term="%22Cytochrome+P-450%22">Cytochrome P-450</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+polymorphism+research%22">Genetic polymorphism research</searchLink><br /><searchLink fieldCode="DE" term="%22Laboratory+mice%22">Laboratory mice</searchLink><br /><searchLink fieldCode="DE" term="%22Medical+research%22">Medical research</searchLink>
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  Data: Abstract: CYP1A2 expression is constitutively high in mouse liver and is well known for metabolizing several drugs and many procarcinogens to reactive intermediates that can cause toxicity or cancer. In the present study, the basal level of hepatic CYP1A2 activity was shown to vary among different inbred mouse strains. The highest methoxyresorufin-O-demethylase activity (261±52pmol/mgprotein/min) was registered in CC57BR and the lowest (82±11pmol/mgprotein/min) in C3H/a. We have tested the hypothesis that possible polymorphisms in regulatory elements in the 5′-upstream region of the mouse CYP1A2 gene could cause the differences in CYP1A2 enzyme activity among different inbred strains. We have performed a study on the CYP1A2 gene by sequencing the regulatory region from −4675 to −4204 where two enhancer elements were recently identified. The absence of mutation prescribing the phenotype in the CYP1A2 gene was found. The region studied seems to be a highly conserved in mice and not to be associated with interstrain differences in constitutive CYP1A2 enzyme activity. [Copyright &y& Elsevier]
– Name: AbstractSuppliedCopyright
  Label:
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  Data: <i>Copyright of Mutation Research - Genetic Toxicology & Environmental Mutagenesis is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1016/j.mrgentox.2007.04.013
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      – Code: eng
        Text: English
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        Type: general
      – SubjectFull: Genetic polymorphism research
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      – SubjectFull: Laboratory mice
        Type: general
      – SubjectFull: Medical research
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      – TitleFull: Enhancer elements in the mouse CYP1A2 gene: A comparative sequencing among different inbred mouse strains
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            NameFull: Filipenko, Maxim L.
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            NameFull: Kaledin, Vasily I.
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              Text: Aug2007
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              Y: 2007
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