The chloroplast division mutant caa33 of Arabidopsis thaliana reveals the crucial impact of chloroplast homeostasis on stress acclimation and retrograde plastid-to-nucleus signaling

Plant J. 2012 Feb;69(4):701-12. doi: 10.1111/j.1365-313X.2011.04825.x. Epub 2011 Dec 16.

Abstract

Retrograde plastid-to-nucleus signaling tightly controls and coordinates the nuclear and plastid gene expression that is required for plastid biogenesis and chloroplast activity. As chloroplasts act as sensors of environmental changes, plastid-derived signaling also modulates stress responses of plants by transferring stress-related signals and altering nuclear gene expression. Various mutant screens have been undertaken to identify constituents of plastid signaling pathways. Almost all mutations identified in these screens target plastid-specific but not extraplastidic functions. They have been suggested to define either genuine constituents of retrograde signaling pathways or components required for the synthesis of plastid signals. Here we report the characterization of the constitutive activator of AAA-ATPase (caa33) mutant, which reveals another way of how mutations that affect plastid functions may modulate retrograde plastid signaling. caa33 disturbs a plastid-specific function by impeding plastid division, and thereby perturbing plastid homeostasis. This results in preconditioning plants by activating the expression of stress genes, enhancing pathogen resistance and attenuating the capacity of the plant to respond to plastid signals. Our study reveals an intimate link between chloroplast activity and the susceptibility of the plant to stress, and emphasizes the need to consider the possible impact of preconditioning on retrograde plastid-to-nucleus signaling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acclimatization / physiology*
  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / metabolism
  • Adenosine Triphosphate / metabolism
  • Alleles
  • Arabidopsis / enzymology
  • Arabidopsis / genetics
  • Arabidopsis / physiology*
  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism
  • Cell Death
  • Cell Nucleus / genetics
  • Cell Nucleus / physiology*
  • Chloroplasts / genetics
  • Chloroplasts / physiology*
  • Gene Expression Regulation, Plant / physiology
  • Homeostasis
  • Light
  • Mesophyll Cells / physiology
  • Mutation
  • Phenotype
  • Signal Transduction / physiology*
  • Singlet Oxygen / metabolism
  • Stress, Physiological / physiology

Substances

  • Arabidopsis Proteins
  • CRUMPLED LEAF protein, Arabidopsis
  • Singlet Oxygen
  • Adenosine Triphosphate
  • Adenosine Triphosphatases