Publication | Open Access
A Putative Peroxisomal Polyamine Oxidase, AtPAO4, is Involved in Polyamine Catabolism in Arabidopsis thaliana
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Citations
35
References
2008
Year
GeneticsPlant BiochemistryMolecular GeneticsAtpao4-deficient MutantsRedox BiologyOxidative StressPlant Molecular BiologyBiosynthesisPlant StressBioenergeticsPlant Gene ExpressionBiochemistryGene ExpressionPlant MetabolismDecreased Spermidine LevelsBiologyArabidopsis ThalianaAtpao4 DeficiencyNatural SciencesPolyamine CatabolismMedicinePlant Physiology
We characterized three Arabidopsis polyamine oxidase genes, AtPAO2, AtPAO3 and AtPAO4. Transient expression of these genes as monomeric red fluorescent protein fusion proteins in Arabidopsis root cells revealed that all are peroxisomal proteins. Quantitative analysis of their transcripts in various organs suggested that AtPAO4 is the major isoform in root peroxisomes. Analysis of recombinant AtPAO4 protein indicated that it is a flavoprotein that catalyzed the oxidative conversion of spermine to spermidine. AtPAO4-deficient mutants established by using T-DNA insertion and RNA interference techniques had markedly increased spermine and decreased spermidine levels in the roots. These results suggest that AtPAO4 is a root peroxisomal polyamine oxidase that participates in polyamine catabolism. Microarray analysis showed that AtPAO4 deficiency induced alterations in the expression of genes related to the drought stress response and flavonoid biosynthesis.
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