Integrated proteome and physiological traits reveal interactive mechanisms of new leaf growth and storage protein degradation with mature leaves of evergreen citrus trees

Tree Physiol. 2024 Feb 11;44(2):tpae001. doi: 10.1093/treephys/tpae001.

Abstract

The growth of fruit trees depends on the nitrogen (N) remobilization in mature tissues and N acquisition from the soil. However, in evergreen mature citrus (Citrus reticulata Blanco) leaves, proteins with N storage functions and hub molecules involved in driving N remobilization remain largely unknown. Here, we combined proteome and physiological analyses to characterize the spatiotemporal mechanisms of growth of new leaves and storage protein degradation in mature leaves of citrus trees exposed to low-N and high-N fertilization in the field. Results show that the growth of new leaves is driven by remobilization of stored reserves, rather than N uptake by the roots. In this context, proline and arginine in mature leaves acted as N sources supporting the growth of new leaves in spring. Time-series analyses with gel electrophoresis and proteome analysis indicated that the mature autumn shoot leaves are probably the sites of storage protein synthesis, while the aspartic endopeptidase protein is related to the degradation of storage proteins in mature citrus leaves. Furthermore, bioinformatic analysis based on protein-protein interactions indicated that glutamate synthetase and ATP-citrate synthetase are hub proteins in N remobilization from mature citrus leaves. These results provide strong physiological data for seasonal optimization of N fertilizer application in citrus orchards.

Keywords: arginine; citrate synthetase; developing leaves; glutamate synthetase; mature leaves; nitrogen mobilization; nitrogen supply; proline; protease.

MeSH terms

  • Citrus* / metabolism
  • Glutamate-Ammonia Ligase / metabolism
  • Nitrogen / metabolism
  • Plant Leaves / physiology
  • Proteolysis
  • Proteome* / metabolism
  • Trees / physiology

Substances

  • Proteome
  • Nitrogen
  • Glutamate-Ammonia Ligase