Functional inactivation of UDP-N-acetylglucosamine pyrophosphorylase 1 (UAP1) induces early leaf senescence and defence responses in rice

J Exp Bot. 2015 Feb;66(3):973-87. doi: 10.1093/jxb/eru456. Epub 2014 Nov 15.

Abstract

Plant leaf senescence and defence responses are important biological processes, but the molecular mechanisms involved are not well understood. This study identified a new rice mutant, spotted leaf 29 (spl29). The SPL29 gene was identified by map-based cloning, and SPL29 was confirmed as UDP-N-acetylglucosamine pyrophosphorylase 1 (UAP1) by enzymatic analysis. The mutant spl29 lacks UAP activity. The biological phenotypes for which UAP is responsible have not previously been reported in plants. The spl29 mutant displayed early leaf senescence, confirmed by chlorophyll loss and photosystem II decline as physiological indicators, chloroplast degradation as a cellular characteristic, and both upregulation of senescence transcription factors and senescence-associated genes, and downregulation of photosynthesis-related genes, as molecular evidence. Defence responses were induced in the spl29 mutant, shown by enhanced resistance to bacterial blight inoculation and upregulation of defence response genes. Reactive oxygen species, including O2 (-) and H2O2, accumulated in spl29 plants; there was also increased malondialdehyde content. Enhanced superoxide dismutase activity combined with normal catalase activity in spl29 could be responsible for H2O2 accumulation. The plant hormones jasmonic acid and abscisic acid also accumulated in spl29 plants. ROS and plant hormones probably play important roles in early leaf senescence and defence responses in the spl29 mutant. Based on these findings, it is suggested that UAP1 is involved in regulating leaf senescence and defence responses in rice.

Keywords: Defence responses; SPL29; UDP-N-acetylglucosamine pyrophosphorylase 1 (UAP1).; leaf senescence; reactive oxygen species (ROS); rice (Oryza sativa).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Mutation
  • Nucleotidyltransferases / genetics*
  • Nucleotidyltransferases / metabolism
  • Oryza / enzymology
  • Oryza / genetics*
  • Oryza / immunology
  • Oryza / metabolism
  • Phylogeny
  • Plant Immunity*
  • Plant Leaves / genetics
  • Plant Leaves / growth & development*
  • Plant Leaves / metabolism
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism

Substances

  • Plant Proteins
  • Nucleotidyltransferases
  • UDPacetylglucosamine pyrophosphorylase