Arabidopsis ATXR2 represses de novo shoot organogenesis in the transition from callus to shoot formation

Cell Rep. 2021 Nov 9;37(6):109980. doi: 10.1016/j.celrep.2021.109980.

Abstract

Plants exhibit high regenerative capacity, which is controlled by various genetic factors. Here, we report that ARABIDOPSIS TRITHORAX-RELATED 2 (ATXR2) controls de novo shoot organogenesis by regulating auxin-cytokinin interaction. The auxin-inducible ATXR2 Trithorax Group (TrxG) protein temporally interacts with the cytokinin-responsive type-B ARABIDOPSIS RESPONSE REGULATOR 1 (ARR1) at early stages of shoot regeneration. The ATXR2-ARR1 complex binds to and deposits the H3K36me3 mark in the promoters of a subset of type-A ARR genes, ARR5 and ARR7, thus activating their expression. Consequently, the ATXR2/ARR1-type-A ARR module transiently represses cytokinin signaling and thereby de novo shoot regeneration. The atxr2-1 mutant calli exhibit enhanced shoot regeneration with low expression of ARR5 and ARR7, which ultimately upregulates WUSCHEL (WUS) expression. Thus, ATXR2 regulates cytokinin signaling and prevents premature WUS activation to ensure proper cell fate transition, and the auxin-cytokinin interaction underlies the initial specification of shoot meristem in callus.

Keywords: Auxin-cytokinin interaction; callus; de novo shoot organogenesis; histone modification; plant regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / cytology*
  • Arabidopsis / genetics
  • Arabidopsis / metabolism
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Cytokinins / metabolism*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation, Plant*
  • Indoleacetic Acids / metabolism*
  • Methyltransferases / genetics
  • Methyltransferases / metabolism
  • Organogenesis*
  • Plant Shoots / cytology*
  • Plant Shoots / genetics
  • Plant Shoots / metabolism
  • Promoter Regions, Genetic
  • Regeneration
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • ARR1 protein, Arabidopsis
  • Arabidopsis Proteins
  • Cytokinins
  • DNA-Binding Proteins
  • Indoleacetic Acids
  • Transcription Factors
  • Methyltransferases