Cytochrome p450 in the house fly: structure, catalytic activity and regulation of expression of CYP6A1 in an insecticide-resistance strain
1995
Feyereisen, R. | Andersen, J.F. | Carino, F.A. | Cohen, M.B. | Koener, J.F.
The house fly P450 CYP6A1 was cloned and sequenced. This gene was mapped to chromosome V of the house fly. Upstream of the transcription start site are sequences (barbie boxes) that may be related to the inducibility of the gene by phenobarbital. The coding sequence of CYP6A1 is interrupted at the Glu364 codon by a single intron of 60 bp, as in five related CYP6 genes that are present on the same chromosome. The catalytic activity of CYP6A1 was analyzed in a reconstituted system of house fly P450 reductase and CYP6A1. The cDNAs for these two components of the microsomal P450 system were expressed in Escherichia coli. CYP6A1 epoxidized the cyclodiene insecticides heptachlor and aldrin at a high rate. The CYP6A1 gene was shown to be constitutively overexpressed in several insecticide-resistant strains, including the multi-resistant Rutgers strain. This high constitutive expression is not caused by an amplification of the CYP6A1 gene. Overexpression of the CYP6A1 gene is controlled by an incompletely dominant locus on chromosome II, both in larvae and in adults. This shows that overexpression is the result of a mutation affecting a trans-acting factor that regulates CYP6A1 expression on chromosome V. Metabolic resistance to insecticides (organophosphorus compounds, carbamates, juvenile hormone analogs etc.) has been mapped repeatedly to chromosome II in the house fly by genetic methods, and these results support the hypothesis of Plapp that a major resistance gene on chromosome II is a regulatory gene.
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