The overexpression of an alternative oxidase triggers ozone sensitivity in tobacco plants (Articolo in rivista)

Type
Label
  • The overexpression of an alternative oxidase triggers ozone sensitivity in tobacco plants (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1111/j.1365-3040.2007.01730.x (literal)
Alternative label
  • Pasqualini S., Paolocci F., Borgogni A., Morettini R., Ederli L (2007)
    The overexpression of an alternative oxidase triggers ozone sensitivity in tobacco plants
    in Plant, cell and environment (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Pasqualini S., Paolocci F., Borgogni A., Morettini R., Ederli L (literal)
Pagina inizio
  • 1545 (literal)
Pagina fine
  • 1556 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 30 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • CNR ISTITUTO GENETICA VEGETALE (literal)
Titolo
  • The overexpression of an alternative oxidase triggers ozone sensitivity in tobacco plants (literal)
Abstract
  • The alternative oxidase (AOX) of plant mitochondria transfers electrons from the ubiquinione pool to oxygen without energy conservation and prevents the formation of reactive oxygen species (ROS) when the ubiquinone pool is over-reduced. Thus,AOX may be involved in plant acclimation to a number of oxidative stresses. To test this hypothesis, we exposed wild-type (WT) Xanthi tobacco plants as well as Xanthi plants transformed with the Bright Yellow tobacco AOX1a cDNA with enhanced (SN21 and SN29), and decreased (SN10)AOX capacity to an acute ozone (O3) fumigation. As a result of 5 h of O3 exposition (250 nL L-1), SN21 and SN29 plants surprisingly showed localized leaf damage, whereas SN10, similarly toWT plants, was undamaged. In keeping with this observation,WT and SN21 plants differed in their response toO3 for the expression profiles of catalase 1 (CAT1), catalase 2 (CAT2), glutathione peroxidase (GPX) and ascorbate peroxidase (APX) genes, and for the activity of these antioxidant enzymes, which were induced in WT. Concomitantly, although ozone induced H2O2 accumulation inWT and in all transgenic lines, only in transgenics with high AOX capacity the H2O2 level in the post-fumigation period was high. The alternative pathway of WT plants was strongly stimulated by O3, whereas in SN21 plants, the respiratory capacity was always high across the treatment. The present results show that, far from exerting a protective role, the overexpression ofAOX triggers an increased O3 sensitivity in tobacco plants. We hypothesize that the AOX overexpression results in a decrease of mitochondrial ROS level that in turn alters the defensive mitochondrial to nucleus signalling pathway that activates ROS scavenging systems. (literal)
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