Do initial S reserves and mineral S availability alter leaf S-N mobilization and leaf senescence in oilseed rape?

Plant Sci. 2011 Mar;180(3):511-20. doi: 10.1016/j.plantsci.2010.11.008. Epub 2010 Nov 26.

Abstract

Winter oilseed rape is sensitive to S limitation, however few studies have clearly assessed the impact of initial S reserves on the remobilization of leaf N-S compounds and senescence dynamics within the leaves in S limited plants. As a consequence, the impacts of high or low initial S reserves on these parameters, further cross-combined with either high or low S availabilities, were examined using a ¹⁵N and ³⁴S double-labelling method associated with a study of gene expression of relevant tonoplastic sulphate transporters (BnSultr4;1 and BnSultr4;2) and a molecular indicator of leaf senescence (BnSAG12/BnCab). Plants with high initial S status and S limitation showed an optimal growth comparable to control plants. Moreover, in response to S limitation, leaf soluble protein content, total S, recently assimilated S (i.e., ³⁴S) and the sulphate content in the oldest leaves declined, and the expression of genes encoding tonoplastic sulphate transporters were up-regulated. However, compared to control plants, S limitation delayed leaf senescence. These data suggested that in response to S limitation, plants with high initial S were able to sustain optimized leaf growth by increasing endogenous N and S remobilization independently of the leaf senescence process. In contrast, if these low S plants had no initial S reserves, leaf N-S remobilization was not sufficient to allow optimal growth. As a conclusion, our study supports a model where oilseed rape is able to compensate transiently for S limitation through a fine management of leaf N-S remobilization and a delayed leaf senescence dynamics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anion Transport Proteins / genetics
  • Anion Transport Proteins / metabolism
  • Biological Transport
  • Brassica rapa / genetics
  • Brassica rapa / growth & development
  • Brassica rapa / metabolism*
  • Cellular Senescence
  • Cysteine Endopeptidases / genetics
  • Cysteine Endopeptidases / metabolism
  • Gene Expression Regulation, Plant*
  • Genes, Plant*
  • Light-Harvesting Protein Complexes / genetics
  • Light-Harvesting Protein Complexes / metabolism
  • Nitrogen / metabolism*
  • Nitrogen Isotopes
  • Photosystem II Protein Complex / genetics
  • Photosystem II Protein Complex / metabolism
  • Plant Leaves / growth & development
  • Plant Leaves / metabolism*
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Solubility
  • Staining and Labeling
  • Sulfates / metabolism
  • Sulfur / metabolism*
  • Sulfur Isotopes
  • Up-Regulation

Substances

  • Anion Transport Proteins
  • Light-Harvesting Protein Complexes
  • Nitrogen Isotopes
  • Photosystem II Protein Complex
  • Plant Proteins
  • Sulfates
  • Sulfur Isotopes
  • Sulfur
  • Cysteine Endopeptidases
  • Nitrogen