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      A codon deletion confers resistance to herbicides inhibiting protoporphyrinogen oxidase.

      Proceedings of the National Academy of Sciences of the United States of America
      Amaranthus, enzymology, genetics, Binding Sites, Codon, Genetic Complementation Test, Halogenated Diphenyl Ethers, Herbicides, metabolism, Models, Molecular, Molecular Sequence Data, Phenyl Ethers, Protoporphyrinogen Oxidase, antagonists & inhibitors

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          Abstract

          Herbicides that act by inhibiting protoporphyrinogen oxidase (PPO) are widely used to control weeds in a variety of crops. The first weed to evolve resistance to PPO-inhibiting herbicides was Amaranthus tuberculatus, a problematic weed in the midwestern United States that previously had evolved multiple resistances to herbicides inhibiting two other target sites. Evaluation of a PPO-inhibitor-resistant A. tuberculatus biotype revealed that resistance was a (incompletely) dominant trait conferred by a single, nuclear gene. Three genes predicted to encode PPO were identified in A. tuberculatus. One gene from the resistant biotype, designated PPX2L, contained a codon deletion that was shown to confer resistance by complementation of a hemG mutant strain of Escherichia coli grown in the presence and absence of the PPO inhibitor lactofen. PPX2L is predicted to encode both plastid- and mitochondria-targeted PPO isoforms, allowing a mutation in a single gene to confer resistance to two herbicide target sites. Unique aspects of the resistance mechanism include an amino acid deletion, rather than a substitution, and the dual-targeting nature of the gene, which may explain why resistance to PPO inhibitors has been rare.

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