Abstract

Plant phosphorus (P) remobilisation during leaf senescence has fundamental implications for global P cycle fluxes. Hypothesising that genes involved in remobilisation of P from leaves during grain filling would show altered expression in response to P deprivation, we investigated gene expression in rice flag leaves at 8 days after anthesis (DAA) and 16 DAA in plants that received a continuous supply of P in the nutrient solution vs plants where P was omitted from the nutrient solution for 8 consecutive days prior to measurement. The transcriptional response to growth in the absence of P differed between the early stage (8 DAA) and the later stage (16 DAA) of grain filling. At 8 DAA, rice plants maintained production of energy substrates through upregulation of genes involved in photosynthesis. In contrast, at 16 DAA carbon substrates were produced by degradation of structural polysaccharides and over 50% of highly upregulated genes in P-deprived plants were associated with protein degradation and nitrogen/amino acid transport, suggesting withdrawal of P from the nutrient solution led to accelerated senescence. Genes involved in liberating inorganic P from the organic P compounds and vacuolar P transporters displayed differential expression depending on the stage of grain filling stage and timing of P withdrawal.

Highlights

  • An estimated 5.7 billion ha of global crop-lands are deficient in bioavailable phosphorus (P) [1]

  • An average of 87.6 ± 0.69% of high quality reads from each replicate were mapped to the rice genome (S2 Table) and distinct Differentially expressed genes (DEGs) retrieved based on log2 fold change

  • The number of DEGs that were upregulated at 8 days after anthesis (DAA) but downregulated at 16 DAA was 142, and 103 DEGs were upregulated at 16 DAA but downregulated at 8 DAA (Fig 1)

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Summary

Introduction

An estimated 5.7 billion ha of global crop-lands are deficient in bioavailable phosphorus (P) [1]. To obtain high yield and maintain soil fertility, regular inputs of P fertiliser, and other nutrients, are required. The efficiency with which applied P fertiliser is utilised by crops is, generally low. Much of the applied P fertiliser becomes ‘fixed’ with iron (Fe) and aluminium (Al) oxides and hydroxides in acid soils, and as calcium (Ca) complexes in alkaline. Transcriptional response of rice flag leaves to P withdrawn

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