4.7 Article

Senescence-inducible cell wall and intracellular purple acid phosphatases: implications for phosphorus remobilization in Hakea prostrata (Proteaceae) and Arabidopsis thaliana (Brassicaceae)

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 65, Issue 20, Pages 6097-6106

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/eru348

Keywords

Arabidopsis thaliana; cell wall hydrolases; Hakea prostrata; phosphorus remobilization; Proteaceae; purple acid phosphatase; ribonuclease; senescence

Categories

Funding

  1. University of Western Australia
  2. Australian Research Council (ARC) [DP1092856]
  3. Natural Sciences and Engineering Research Council of Canada
  4. Queen's Research Chairs program
  5. Australian Research Council [DP1092856] Funding Source: Australian Research Council

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Despite its agronomic importance, the metabolic networks mediating phosphorus (P) remobilization during plant senescence are poorly understood. Highly efficient P remobilization (similar to 85%) from senescing leaves and proteoid roots of harsh hakea (Hakea prostrata), a native 'extremophile' plant of south-western Australia, was linked with striking up-regulation of cell wall-localized and intracellular acid phosphatase (APase) and RNase activities. Non-denaturing PAGE followed by in-gel APase activity staining revealed senescence-inducible 120 kDa and 60 kDa intracellular APase isoforms, whereas only the 120 kDa isoform was detected in corresponding cell wall fractions. Kinetic and immunological properties of the 120 kDa and 60 kDa APases partially purified from senescing leaves indicated that they are purple acid phosphatases (PAPs). Results obtained with cell wall-targeted hydrolases of harsh hakea were corroborated using Arabidopsis thaliana in which an similar to 200% increase in cell wall APase activity during leaf senescence was paralleled by accumulation of immunoreactive 55 kDa AtPAP26 polypeptides. Senescing leaves of an atpap26 T-DNA insertion mutant displayed a >90% decrease in cell wall APase activity. Previous research established that senescing leaves of atpap26 plants exhibited a similar reduction in intracellular (vacuolar) APase activity, while displaying markedly impaired P remobilization efficiency and delayed senescence. It is hypothesized that up-regulation and dual targeting of PAPs and RNases to the cell wall and vacuolar compartments make a crucial contribution to highly efficient P remobilization that dominates the P metabolism of senescing tissues of harsh hakea and Arabidopsis. To the best of the authors' knowledge, the apparent contribution of cell wall-targeted hydrolases to remobilizing key macronutrients such as P during senescence has not been previously suggested.

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