Hydrogen peroxide participates in leaf senescence by inhibiting CHLI1 activity

Plant Cell Rep. 2024 Oct 9;43(11):258. doi: 10.1007/s00299-024-03350-4.

Abstract

Hydrogen peroxide promoted leaf senescence by sulfenylating the magnesium chelating protease I subunit (CHLI1) in the chlorophyll synthesis pathway, and inhibited its activity to reduce chlorophyll synthesis. Leaf senescence is the final and crucial stage of plant growth and development, during which chlorophyll experiences varying degrees of destruction. It is well-known that the higher ROS accumulation is a key factor for leaf senescence, but whether and how ROS regulates chlorophyll synthesis in the process are unknown. Here, we report that H2O2 inhibits chlorophyll synthesis during leaf senescence via the I subunit of magnesium-chelatase (CHLI1). During leaf senescence, the decrease of chlorophyll content is accompanied by the increase of H2O2 accumulation, as well as the inhibition of catalase (CAT) genes expression. The mutant cat2-1, with increased H2O2 shows an accelerated senescence phenotype and decreased CHLI1 activity compared with the wild type. H2O2 inhibits CHLI1 activity by sulfenylating CHLI1 during leaf senescence. Consistent with this, the chli1 knockout mutant displays the same premature leaf senescence symptom as cat2-1, while overexpression of CHLI1 in cat2-1 can partially restore its early senescence phenotype. Taken together, these results illustrate that CAT2-mediated H2O2 accumulation during leaf senescence represses chlorophyll synthesis through sulfenylating CHLI1, and thus inhibits its activity, providing a new insight into the pivotal role of chlorophyll synthesis as a participant in orchestrating the leaf senescence.

Keywords: CAT2; CHLI1; H2O2; Leaf senescence.

MeSH terms

  • Arabidopsis Proteins* / genetics
  • Arabidopsis Proteins* / metabolism
  • Arabidopsis* / drug effects
  • Arabidopsis* / genetics
  • Arabidopsis* / growth & development
  • Arabidopsis* / metabolism
  • Arabidopsis* / physiology
  • Catalase* / metabolism
  • Chlorophyll* / metabolism
  • Gene Expression Regulation, Plant* / drug effects
  • Hydrogen Peroxide* / metabolism
  • Lyases
  • Plant Leaves* / drug effects
  • Plant Leaves* / genetics
  • Plant Leaves* / growth & development
  • Plant Leaves* / metabolism
  • Plant Senescence* / genetics
  • Reactive Oxygen Species / metabolism

Substances

  • Chlorophyll
  • Hydrogen Peroxide
  • Arabidopsis Proteins
  • Catalase
  • magnesium chelatase
  • CAT2 protein, Arabidopsis
  • Reactive Oxygen Species
  • Lyases