Resistance of insect pests to insecticides is a major problem worldwide and has appeared in over 170 arthropod species of public health importance. Increased detoxification of insecticides by cytochrome P450 enzymes is a major mechanism of resistance, but its molecular basis is unknown. The long term objective of this proposal is to study the structure, function and regulation of insect cytochrome P450 genes and proteins. This basic knowledge is needed to understand the molecular basis of insecticide resistance in insects as well as the diversity and evolution of P450 genes. This knowledge will be needed in resistance management programs which are becoming a part of integrated pest management systems. The proposal focuses on insecticide-resistant and susceptible strains of the house fly, Musca domestica, and will continue the studies which have already yielded cDNAs clones and sequences for a cytochrome P450 and for NADPH:cytochrome P450 reductase.
The specific aims of this proposal are:(l) To elucidate the structure of P450 genes and proteins: The effort to clone and sequence P450 cDNAs will be continued in order to characterize those P450s involved in insecticide resistance and to document the multiplicity of P450 in insects. This effort will be supported in part by a new technique to obtain probes for P450 proteins based on photoaffinity labeling. The sequences of P450 proteins and the intron-exon organization of the P450 genes will be compared and their evolutionary relationships will be studied. (2) To define the function of P450 proteins: Polyclonal antibodies to P450 polypeptides expressed in bacteria and to P450 peptide segments will be raised. An expression system for P450 proteins and fusion proteins of P450 reductase and cytochrome P450 in yeast will be developed. Inhibition of microsomal P450 activity by antibodies and assays of P450 expressed in yeast will be used to define what reactions are catalyzed by individual P450 proteins. (3) To study the regulation of P450 gene expression and the molecular basis of P450-mediated insecticide resistance: The hypothesis that insecticide resistance in the Rutgers strain is caused by an altered (increased) P450 gene expression will be tested. Evidence for the existence of trans-acting factor(s) will be sought and trans-regulation of P450 gene expression will be investigated.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM039014-07
Application #
3295767
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1991-01-01
Project End
1995-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
7
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Arizona
Department
Type
Schools of Earth Sciences/Natur
DUNS #
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Giraudo, Maeva; Unnithan, G Chandran; Le Goff, Gaƫlle et al. (2010) Regulation of cytochrome P450 expression in Drosophila: Genomic insights. Pestic Biochem Physiol 97:115-122
Murataliev, Marat B; Guzov, Victor M; Walker, F Ann et al. (2008) P450 reductase and cytochrome b5 interactions with cytochrome P450: effects on house fly CYP6A1 catalysis. Insect Biochem Mol Biol 38:1008-15
Jacobsen, Neil E; Kover, Katalin E; Murataliev, Marat B et al. (2006) Structure and stereochemistry of products of hydroxylation of human steroid hormones by a housefly cytochrome P450 (CYP6A1). Magn Reson Chem 44:467-74
Helvig, Christian; Tijet, Nathalie; Feyereisen, Rene et al. (2004) Drosophila melanogaster CYP6A8, an insect P450 that catalyzes lauric acid (omega-1)-hydroxylation. Biochem Biophys Res Commun 325:1495-502
Murataliev, Marat B; Trinh, Long N; Moser, Lani V et al. (2004) Chimeragenesis of the fatty acid binding site of cytochrome P450BM3. Replacement of residues 73-84 with the homologous residues from the insect cytochrome P450 CYP4C7. Biochemistry 43:1771-80
Murataliev, Marat B; Feyereisen, Rene; Walker, F Ann (2004) Electron transfer by diflavin reductases. Biochim Biophys Acta 1698:1-26
Tijet, N; Helvig, C; Feyereisen, R (2001) The cytochrome P450 gene superfamily in Drosophila melanogaster: annotation, intron-exon organization and phylogeny. Gene 262:189-98
Sabourault, C; Guzov, V M; Koener, J F et al. (2001) Overproduction of a P450 that metabolizes diazinon is linked to a loss-of-function in the chromosome 2 ali-esterase (MdalphaE7) gene in resistant house flies. Insect Mol Biol 10:609-18
Murataliev, M B; Feyereisen, R (2000) Functional interactions in cytochrome P450BM3. Evidence that NADP(H) binding controls redox potentials of the flavin cofactors. Biochemistry 39:12699-707
Murataliev, M B; Feyereisen, R (2000) Interaction of NADP(H) with oxidized and reduced P450 reductase during catalysis. Studies with nucleotide analogues. Biochemistry 39:5066-74

Showing the most recent 10 out of 30 publications