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Vol. 30, Issue 10, 1043-1052, October 2002
Human BioMolecular Research Institute, San Diego, California
The human flavin-containing monooxygenase (form 3) (FMO3)
participates in the oxygenation of nucleophilic heteroatom-containing drugs, xenobiotics, and endogenous materials. Currently, six forms of
the FMO gene are known, but it is FMO3 that is the major
form in adult human liver that is likely responsible for the majority of FMO-mediated metabolism. The substrate structural feature
requirements for human FMO3 is beginning to become known to a greater
extent and a few chemicals extensively metabolized by FMO3 have been reported. Expression of FMO3 is species- and tissue-specific, but
unlike human cytochrome P450, mammalian FMO3 does not appear to be
inducible. Interindividual variation in FMO3-dependent metabolism of
drugs, chemicals, and endogenous material is therefore more likely due
to genetic effects and not environmental ones. Examples of such
interindividual variation come from the study of very rare mutations of
the human FMO3 gene that have been associated with
deficient N-oxygenation of dietary trimethylamine.
Defective trimethylamine N-oxygenation causes
trimethylaminuria or "fish-like odor syndrome". Information on
human FMO3 mutations from individuals suffering from the
condition of trimethylaminuria has provided knowledge about the
underlying molecular mechanism(s) for trimethylaminuria. A number of
common variants of human FMO3 have been reported. Diversification of the FMO3 gene may have led to
selective advantages and new functions. As more examples of human
FMO3-mediated metabolism of drugs or new chemical entities are
discovered in the future, it is possible that FMO3
allelic variation may be shown to contribute to interindividual and
interethnic variability of FMO-mediated metabolism. Human
FMO3 may be another example of an environmental gene
that participates in a protective mechanism to help humans ward off
potentially toxic exposure of chemicals.
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