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Evolution of a Major Drug Metabolizing Enzyme Defect in the Domestic Cat and Other Felidae: Phylogenetic Timing and the Role of Hypercarnivory

Overview of attention for article published in PLOS ONE, March 2011
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Title
Evolution of a Major Drug Metabolizing Enzyme Defect in the Domestic Cat and Other Felidae: Phylogenetic Timing and the Role of Hypercarnivory
Published in
PLOS ONE, March 2011
DOI 10.1371/journal.pone.0018046
Pubmed ID
Authors

Binu Shrestha, J. Michael Reed, Philip T. Starks, Gretchen E. Kaufman, Jared V. Goldstone, Melody E. Roelke, Stephen J. O'Brien, Klaus-Peter Koepfli, Laurence G. Frank, Michael H. Court

Abstract

The domestic cat (Felis catus) shows remarkable sensitivity to the adverse effects of phenolic drugs, including acetaminophen and aspirin, as well as structurally-related toxicants found in the diet and environment. This idiosyncrasy results from pseudogenization of the gene encoding UDP-glucuronosyltransferase (UGT) 1A6, the major species-conserved phenol detoxification enzyme. Here, we established the phylogenetic timing of disruptive UGT1A6 mutations and explored the hypothesis that gene inactivation in cats was enabled by minimal exposure to plant-derived toxicants. Fixation of the UGT1A6 pseudogene was estimated to have occurred between 35 and 11 million years ago with all extant Felidae having dysfunctional UGT1A6. Out of 22 additional taxa sampled, representative of most Carnivora families, only brown hyena (Parahyaena brunnea) and northern elephant seal (Mirounga angustirostris) showed inactivating UGT1A6 mutations. A comprehensive literature review of the natural diet of the sampled taxa indicated that all species with defective UGT1A6 were hypercarnivores (>70% dietary animal matter). Furthermore those species with UGT1A6 defects showed evidence for reduced amino acid constraint (increased dN/dS ratios approaching the neutral selection value of 1.0) as compared with species with intact UGT1A6. In contrast, there was no evidence for reduced amino acid constraint for these same species within UGT1A1, the gene encoding the enzyme responsible for detoxification of endogenously generated bilirubin. Our results provide the first evidence suggesting that diet may have played a permissive role in the devolution of a mammalian drug metabolizing enzyme. Further work is needed to establish whether these preliminary findings can be generalized to all Carnivora.

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Geographical breakdown

Country Count As %
United States 2 1%
United Kingdom 2 1%
Brazil 2 1%
Colombia 1 <1%
Germany 1 <1%
Austria 1 <1%
Turkey 1 <1%
Portugal 1 <1%
United Arab Emirates 1 <1%
Other 3 2%
Unknown 157 91%

Demographic breakdown

Readers by professional status Count As %
Researcher 36 21%
Student > Master 24 14%
Student > Bachelor 24 14%
Student > Ph. D. Student 19 11%
Other 16 9%
Other 31 18%
Unknown 22 13%
Readers by discipline Count As %
Agricultural and Biological Sciences 83 48%
Environmental Science 21 12%
Veterinary Science and Veterinary Medicine 9 5%
Biochemistry, Genetics and Molecular Biology 8 5%
Medicine and Dentistry 7 4%
Other 16 9%
Unknown 28 16%