Characterization of thioredoxin gene TaTrxh9 associated with heading-time regulation in wheat

Plant Physiol Biochem. 2023 Aug:201:107903. doi: 10.1016/j.plaphy.2023.107903. Epub 2023 Jul 21.

Abstract

Thioredoxins (Trxs) are thiol-disulfide oxidoreductase proteins that play important roles in a spectrum of processes linking redox regulation and signaling in plants. However, little is known about Trxs and their biological functions in wheat, one of the most important food crops worldwide. This study reports the identification and functional characterization of an h-type Trx gene, TaTrxh9, in wheat. Three homoeologs of TaTrxh9 were identified and the sequences in the coding region were highly consistent among the homoeologs. Protein characterization showed that a conserved Trx_family domain, as well as a typical active site with a dithiol signature (WCGPC), was included in TaTrxh9. Structural modeling demonstrated that TaTrxh9 could fold into a canonical thioredoxin structure consisting of five-stranded antiparallel beta sheets sandwiched between four alpha helices. The insulin disulfide reduction assay demonstrated that TaTrxh9 was catalytically active in vitro. TaTrxh9 overexpression in the Arabidopsis mutant trxh9 complemented the abnormal growth phenotypes of the mutant, suggesting is functionality in vivo. The transcription level of TaTrxh9 was higher in leaf tissues and it was differentially expressed during the development of wheat plants. Interestingly, barley stripe mosaic virus-mediated suppression of TaTrxh9 shortened the seedling-heading period of wheat. Furthermore, CRISPR-Cas9 mediated gene knockout confirmed that the TaTrxh9 mutation resulted in early heading of wheat. To our knowledge, this study is the first to report that Trxh is associated with heading-time regulation, which lays a foundation for further exploring the biological function of TaTrxh9 and provides new ideas for molecular breeding focusing on early heading in wheat.

Keywords: Catalytic activity; Development; Gene expression; Gene knockout; Homoeologs; Redox regulation.

MeSH terms

  • Arabidopsis* / genetics
  • Arabidopsis* / metabolism
  • Oxidation-Reduction
  • Plants / metabolism
  • Thioredoxins / chemistry
  • Thioredoxins / genetics
  • Thioredoxins / metabolism
  • Triticum* / genetics
  • Triticum* / metabolism

Substances

  • Thioredoxins