The gene NtMYC2a acts as a 'master switch' in the regulation of JA-induced nicotine accumulation in tobacco

Plant Biol (Stuttg). 2021 Mar;23(2):317-326. doi: 10.1111/plb.13223. Epub 2021 Jan 13.

Abstract

The biosynthesis and transport of nicotine has been shown to be coordinately upregulated by jasmonate (JA). MYC2, a member of basic helix-loop-helix (bHLH) transcription factor family, is well-documented as the core player in the JA signalling pathway to regulate diverse plant development processes. Four MYC2 genes were found in the tobacco genome, NtMYC2a/2b and 1a/1b. In this study, we tested whether one of them, NtMYC2a, acts as a 'master switch' in the regulation of nicotine biosynthesis and transport in tobacco. We generated NtMYC2a knockout tobacco plants using the CRISPR-Cas9 technique and analysed the effect of NtMYC2a knockout on expression of the nicotine biosynthesis genes (NtAO, NtQS, NtPMT1a, NtQPT2, NtODC2, NtMPO1, NtA622 and NtBBLa) and transport genes (NtMATE2 and NtJAT1), as well as leaf accumulation of nicotine in the NtMYC2a knockout plants. We found that all the nicotine biosynthesis and transport genes tested in this study were significantly downregulated (>50% reduction compared with wild-type control) in the NtMYC2a knockout plants. Moreover, the leaf nicotine content in knockout plants was dramatically reduced by ca 80% compared with the wild-type control. These results clearly show that NtMYC2a acts as a 'master switch' to coordinate JA-induced nicotine accumulation in tobacco and suggests that NtMYC2a might play an important role in tobacco nicotine-mediated defence against herbivory.

Keywords: NtMYC2a; coordinated regulation; master switch; nicotine; tobacco.

MeSH terms

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors* / metabolism
  • Cyclopentanes* / pharmacology
  • Gene Expression Regulation, Plant* / genetics
  • Nicotiana* / drug effects
  • Nicotiana* / genetics
  • Nicotiana* / metabolism
  • Nicotine* / metabolism
  • Oxylipins* / pharmacology
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Plants, Genetically Modified / metabolism

Substances

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Cyclopentanes
  • Oxylipins
  • Plant Proteins
  • Nicotine
  • jasmonic acid