Mitochondrial Biogenesis in Diverse Cauliflower Cultivars under Mild and Severe Drought. Impaired Coordination of Selected Transcript and Proteomic Responses, and Regulation of Various Multifunctional Proteins

Int J Mol Sci. 2018 Apr 10;19(4):1130. doi: 10.3390/ijms19041130.

Abstract

Mitochondrial responses under drought within Brassica genus are poorly understood. The main goal of this study was to investigate mitochondrial biogenesis of three cauliflower (Brassica oleracea var. botrytis) cultivars with varying drought tolerance. Diverse quantitative changes (decreases in abundance mostly) in the mitochondrial proteome were assessed by two-dimensional gel electrophoresis (2D PAGE) coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS). Respiratory (e.g., complex II, IV (CII, CIV) and ATP synthase subunits), transporter (including diverse porin isoforms) and matrix multifunctional proteins (e.g., components of RNA editing machinery) were diversely affected in their abundance under two drought levels. Western immunoassays showed additional cultivar-specific responses of selected mitochondrial proteins. Dehydrin-related tryptic peptides (found in several 2D spots) immunopositive with dehydrin-specific antisera highlighted the relevance of mitochondrial dehydrin-like proteins for the drought response. The abundance of selected mRNAs participating in drought response was also determined. We conclude that mitochondrial biogenesis was strongly, but diversely affected in various cauliflower cultivars, and associated with drought tolerance at the proteomic and functional levels. However, discussed alternative oxidase (AOX) regulation at the RNA and protein level were largely uncoordinated due to the altered availability of transcripts for translation, mRNA/ribosome interactions, and/or miRNA impact on transcript abundance and translation.

Keywords: 2D PAGE; dehydrins; drought; mitochondrial biogenesis; mitochondrial proteome; plant transcriptome.

MeSH terms

  • ATP Synthetase Complexes / genetics
  • ATP Synthetase Complexes / metabolism
  • Brassica / metabolism*
  • Droughts
  • Electron Transport Complex II / genetics
  • Electron Transport Complex II / metabolism
  • Gene Expression Regulation, Plant
  • Organelle Biogenesis*
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Porins / genetics
  • Porins / metabolism
  • Proteome / genetics*
  • Proteome / metabolism
  • Stress, Physiological*
  • Transcriptome*

Substances

  • Plant Proteins
  • Porins
  • Proteome
  • respiratory complex II
  • Electron Transport Complex II
  • ATP Synthetase Complexes