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Vol. 30, Issue 9, 1022-1028, September 2002
Department of Biochemistry and Molecular Biology, the University of
Texas Medical School of Houston, Houston, Texas
The cytochromes P450 belong to a superfamily of enzymes involved in
a diverse array of endobiotic and xenobiotic metabolic pathways.
Several members of a novel family of cytochrome P450 (CYP4F), which
specifically mediate leukotriene B4
-hydroxylation, have now been identified in various species
including rat, mouse, and human. In rats, the CYP4F family consists of
four related genes, CYP4F1, CYP4F4, CYP4F5, and CYP4F6. Here we report
development of fluorescent real-time quantitative polymerase chain
reaction assays (TaqMan), which allow us to carry out specific
quantitation of mRNA expression of all four members of this subfamily.
Since no inducers for the CYP4F family are known to date, we validated these assays using clofibrate, a known suppressor of rat CYP4Fs. Additionally, Northern blot hybridization was carried out to validate these assays. Using this approach, we demonstrate quantitatively, for
the first time, that each of the rat CYP4Fs is expressed in a tissue-
and sex-dependent manner showing a significantly higher expression in
females vis-à-vis males. Western blot analysis using a CYP4F
polyclonal antibody also shows a considerably higher protein expression
in female liver, kidneys, and lungs when compared with male rats.
Furthermore, we observe a significant decrease in the CYP4F1, CYP4F4,
and CYP4F6 message in kidneys and liver of ovariectomized rats when
compared with control females. This loss of expression is partially
restored by estrogen treatment in both tissues, suggesting a role of
estrogen in regulating CYP4F expression.
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