Transcriptomics Reveals the ERF2- bHLH2- CML5 Module Responses to H2S and ROS in Postharvest Calcium Deficiency Apples

Int J Mol Sci. 2021 Dec 1;22(23):13013. doi: 10.3390/ijms222313013.

Abstract

Calcium deficiency usually causes accelerated quality deterioration in postharvest fruit, whereas the underlining mechanism is still unclear. Here, we report that calcium deficiency induced the development of bitter pit on the surface of apple peels compared with the healthy appearance in control apples during postharvest storage. Physiological analysis indicates that calcium-deficient peels contained higher levels of superoxide anion (O2•-), malondialdehyde (MDA), total phenol, flavonoid contents and polyphenol oxidase (PPO) activity, and reduced calcium, H2S production, anthocyanin, soluble protein content, and peroxidase (POD) activity compared with those in calcium-sufficient peels. The principal component analysis (PCA) results show that calcium content, ROS, and H2S production were the main factors between calcium-deficient and calcium-sufficient apple peels. Transcriptome data indicated that four calmodulin-like proteins (CMLs), seven AP2/ERFs, and three bHLHs transcripts were significantly differentially expressed in calcium-deficient apple peels. RT-qPCR and correlation analyses further revealed that CML5 expression was significantly positively correlated with the expression of ERF2/17, bHLH2, and H2S production related genes. In addition, transcriptional co-activation of CML5 by ERF2 and bHLH2 was demonstrated by apple transient expression assays and dual-luciferase reporter system experiments. Therefore, these findings provide a basis for studying the molecular mechanism of postharvest quality decline in calcium-deficient apples and the potential interaction between Ca2+ and endogenous H2S.

Keywords: ERF2-bHLH2-CML5 module; calcium deficiency; endogenous H2S; postharvest storage quality; reactive oxygen species.

MeSH terms

  • Anthocyanins / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Calcium / metabolism
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / metabolism
  • Catechol Oxidase / metabolism
  • Flavonoids / metabolism
  • Food Storage
  • Fruit / genetics
  • Fruit / metabolism
  • Hydrogen Sulfide / metabolism*
  • Malus / genetics
  • Malus / metabolism*
  • Peptide Termination Factors / genetics
  • Peptide Termination Factors / metabolism
  • Phenols / metabolism
  • Phenotype
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Principal Component Analysis
  • Reactive Oxygen Species / metabolism*
  • Transcriptome*

Substances

  • Anthocyanins
  • Basic Helix-Loop-Helix Transcription Factors
  • Calcium-Binding Proteins
  • Flavonoids
  • Peptide Termination Factors
  • Phenols
  • Plant Proteins
  • Reactive Oxygen Species
  • Catechol Oxidase
  • Calcium
  • Hydrogen Sulfide