Interaction between plastid and mitochondrial retrograde signalling pathways during changes to plastid redox status

Philos Trans R Soc Lond B Biol Sci. 2014 Mar 3;369(1640):20130231. doi: 10.1098/rstb.2013.0231. Print 2014 Apr 19.

Abstract

Mitochondria and chloroplasts depend upon each other; photosynthesis provides substrates for mitochondrial respiration and mitochondrial metabolism is essential for sustaining photosynthetic carbon assimilation. In addition, mitochondrial respiration protects photosynthesis against photoinhibition by dissipating excess redox equivalents from the chloroplasts. Genetic defects in mitochondrial function result in an excessive reduction and energization of the chloroplast. Thus, it is clear that the activities of mitochondria and plastids need to be coordinated, but the manner by which the organelles communicate to coordinate their activities is unknown. The regulator of alternative oxidase (rao1) mutant was isolated as a mutant unable to induce AOX1a expression in response to the inhibitor of the mitochondrial cytochrome c reductase (complex III), antimycin A. RAO1 encodes the nuclear localized cyclin-dependent kinase E1 (CDKE1). Interestingly, the rao1 mutant demonstrates a genome uncoupled phenotype also in response to redox changes in the photosynthetic electron transport chain. Thus, CDKE1 was shown to regulate both LIGHT HARVESTING COMPLEX B (LHCB) and ALTERNATIVE OXIDASE 1 (AOX1a) expression in response to retrograde signals. Our results suggest that CDKE1 is a central nuclear component integrating mitochondrial and plastid retrograde signals and plays a role in regulating energy metabolism during the response to stress.

Keywords: chloroplast; kinase; mitochondria; redox; retrograde.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimycin A / analogs & derivatives
  • Antimycin A / metabolism
  • Arabidopsis / physiology*
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Chloroplasts / metabolism
  • Chloroplasts / physiology*
  • Cyclin-Dependent Kinases / genetics
  • Cyclin-Dependent Kinases / metabolism*
  • DNA Primers / genetics
  • Electron Transport / physiology
  • Gene Expression Regulation, Plant / genetics
  • Gene Expression Regulation, Plant / physiology*
  • Light-Harvesting Protein Complexes / metabolism
  • Mitochondria / physiology*
  • Mitochondrial Proteins / metabolism
  • Mutation / genetics
  • Oxidation-Reduction
  • Oxidoreductases / metabolism
  • Plant Proteins / metabolism
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction / physiology*

Substances

  • Arabidopsis Proteins
  • CAB2 protein, Arabidopsis
  • DNA Primers
  • Light-Harvesting Protein Complexes
  • Mitochondrial Proteins
  • Plant Proteins
  • antimycin
  • Antimycin A
  • Oxidoreductases
  • alternative oxidase
  • Cyclin-Dependent Kinases
  • cyclin-dependent kinase E1, Arabidopsis