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Insect cytochromes P450: diversity, insecticide resistance and tolerance to plant toxins
Open accessAbstract
In the last decade, studies of individual insect P450s have blossomed. This new information has furthered our understanding of P450 diversity, insecticide resistance and tolerance to plant toxins. Insect P450s can be adult specific, larval specific or life stage independent. Similarly, insect P450s vary as to the tissues where they are expressed and in their response to inducers. Insect P450s can now be rapidly sequenced using degenerate PCR primers. Given the huge diversity represented by the Class Insecta, this technique will provide vast amounts of new information about insect P450s and the evolution of the P450 gene superfamily. CYP6D1 is responsible for monooxygenase-mediated resistance to pyrethroid insecticides in the house fly. CYP6D1 is ubiquitously expressed in adults with 10-fold higher levels found in the resistant strain compared to susceptible strains. CYP6D1 is on autosome 1 in house fly. The high level of expression found in the resistant strain is due to genes on autosomes 1 and 2. Whether or not the different CYP6D1 alleles found in resistant and susceptible strains have any role in resistance remains to be elucidated. The CYP6B gene subfamily is involved in the metabolism of host plant toxins (i.e. furanocoumarins). CYP6B gene transcripts in two Papilio (swallowtail) species have been shown to be induced by host plant toxins and in turn to metabolize these toxins. CYP6B P450s play a critical role in allowing Papilio to adapt to furanocoumarin-containing host plants. Similarities in structural and promoter regions of the CYP6B genes suggest that they are derived from a common ancestral gene. Although the P450 monooxygenases of insects are important for the metabolism of hormones and phermones, no individual P450 has yet been shown to metabolize an endogenous compound. Advances in this area are critical because they will provide important new information about insect physiology, biochemistry and development.
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Cited by
Mao, Y.-B., Cai, W.-J., Wang, J.-W., Hong, G.-J., Tao, X.-Y., Wang, L.-J., Huang, Y.-P., & Chen, X.-Y. (2007) · Nature Biotechnology · doi:10.1038/nbt1352 · Cited by 1,358
Kennedy, D. O., & Wightman, E. L. (2011) · Advances in Nutrition · doi:10.3945/an.110.000117 · Cited by 684
Smith, L. B., Kasai, S., & Scott, J. G. (2016) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2016.03.005 · Cited by 405
Self-citationThe molecular basis of two contrasting metabolic mechanisms of insecticide resistance
Hemingway, J. (2000) · Insect Biochemistry and Molecular Biology · doi:10.1016/s0965-1748(00)00079-5 · Cited by 345
Recent advances in allelopathy for weed control: from knowledge to applications
Macías, F. A., Mejías, F. J., & Molinillo, J. M. (2019) · Pest Management Science · doi:10.1002/ps.5355 · Cited by 293
Metadata
- Authors
- Scott, J. G., Liu, N., & Wen, Z.
- Venue
- Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology
- Publisher
- Elsevier BV
- Published
- 1998-11
- Volume
- 121
- Issue
- 1-3
- Pages
- 147-155
- ISSN
- 0742-8413 (ISSN-L)
- OpenAlex
- W2079498128
- Cited by
- 242
- References
- 0
- FWCI
- 1.80
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Scott, J. G., Liu, N., & Wen, Z. (1998). Insect cytochromes P450: diversity, insecticide resistance and tolerance to plant toxins. Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology. https://doi.org/10.1016/s0742-8413(98)10035-x
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