Molecular Properties and Functional Divergence of the Dehydroascorbate Reductase Gene Family in Lower and Higher Plants

PLoS One. 2015 Dec 18;10(12):e0145038. doi: 10.1371/journal.pone.0145038. eCollection 2015.

Abstract

Dehydroascorbate reductase (DHAR), which reduces oxidized ascorbate, is important for maintaining an appropriate ascorbate redox state in plant cells. To date, genome-wide molecular characterization of DHARs has only been conducted in bryophytes (Physcomitrella patens) and eudicots (e.g. Arabidopsis thaliana). In this study, to gain a general understanding of the molecular properties and functional divergence of the DHARs in land plants, we further conducted a comprehensive analysis of DHARs from the lycophyte Selaginella moellendorffii, gymnosperm Picea abies and monocot Zea mays. DHARs were present as a small gene family in all of the land plants we examined, with gene numbers ranging from two to four. All the plants contained cytosolic and chloroplastic DHARs, indicating dehydroascorbate (DHA) can be directly reduced in the cytoplasm and chloroplast by DHARs in all the plants. A novel vacuolar DHAR was found in Z. mays, indicating DHA may also be reduced in the vacuole by DHARs in Z. mays. The DHARs within each species showed extensive functional divergence in their gene structures, subcellular localizations, and enzymatic characteristics. This study provides new insights into the molecular characteristics and functional divergence of DHARs in land plants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chloroplasts / enzymology
  • Cytosol / enzymology
  • Gene Expression Regulation, Plant
  • Multigene Family
  • Oxidoreductases / genetics*
  • Oxidoreductases / metabolism*
  • Phylogeny
  • Picea / cytology
  • Picea / enzymology*
  • Picea / genetics
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Selaginellaceae / cytology
  • Selaginellaceae / enzymology*
  • Selaginellaceae / genetics
  • Sequence Analysis, DNA
  • Vacuoles / enzymology
  • Zea mays / cytology
  • Zea mays / enzymology*
  • Zea mays / genetics

Substances

  • Plant Proteins
  • Oxidoreductases
  • glutathione dehydrogenase (ascorbate)

Grants and funding

This study was supported by grants from the Natural Science Foundation of China (NSFC 31270641). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.