Lipid peroxidation during the hypersensitive response in potato in the absence of 9-lipoxygenases

J Biol Chem. 2003 Dec 26;278(52):52834-40. doi: 10.1074/jbc.M310833200. Epub 2003 Oct 9.

Abstract

Hypersensitive cell death is an important defense reaction of plants to pathogen infection and is accompanied by lipid peroxidation processes. These may occur non-enzymatically by the action of reactive oxygen species or may be catalyzed by enzymes such as alpha-dioxygenases, lipoxygenases, or peroxidases. Correlative data showing increases in 9-lipoxygenase products in hyper-sensitively reacting cells have so far suggested that a large part of lipid peroxidation is mediated by a specific set of 9-lipoxygenases. To address the significance of 9-lipoxygenases for this type of pathogen response in potato, RNA interference constructs of a specific pathogen-induced potato 9-lipoxygenase were transferred to potato plants. Significantly reduced 9-lipoxygenase transcript levels were observed in transgenic plants after pathogen treatment. In addition, 9-lipoxygenase activity was hardly detectable, and levels of 9-lipoxygenase-derived oxylipins were reduced up to 12-fold after pathogen infection. In contrast to wild type plants, high levels of non-enzymatically as well as 13-lipoxygenase-derived oxylipins were present in 9-lipoxygenase-deficient plants. From this we conclude that during the normal hypersensitive response in potato, lipid peroxidation may occur as a controlled and directed process that is facilitated by the action of a specific 9-lipoxygenase. If 9-lipoxygenase-mediated formation of hydroperoxides is repressed, autoxidative lipid peroxidation processes and 13-lipoxygenase-mediated oxylipins synthesis become prominent. The unaltered timing and extent of necrosis formation suggests that the origin of lipid hydroperoxides does not influence pathogen-induced cell death in potato.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Death
  • Chromatography, High Pressure Liquid
  • Cloning, Molecular
  • DNA, Complementary / metabolism
  • Genetic Vectors
  • Lipid Peroxidation
  • Lipid Peroxides
  • Lipoxygenase / metabolism
  • Lipoxygenase / physiology*
  • Plant Leaves
  • Plants, Genetically Modified
  • Protein Isoforms
  • RNA / metabolism
  • RNA Interference
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species
  • Solanum tuberosum / genetics
  • Solanum tuberosum / metabolism*
  • Time Factors

Substances

  • DNA, Complementary
  • Lipid Peroxides
  • Protein Isoforms
  • RNA, Messenger
  • Reactive Oxygen Species
  • RNA
  • 13-lipoxygenase
  • Lipoxygenase