Alterations of plant architecture and phase transition by the phytoplasma virulence factor SAP11

J Exp Bot. 2018 Nov 26;69(22):5389-5401. doi: 10.1093/jxb/ery318.

Abstract

As key mediators linking developmental processes with plant immunity, TCP (TEOSINTE-BRANCHED, CYCLOIDEA, PROLIFERATION FACTOR 1 and 2) transcription factors have been increasingly shown to be targets of pathogenic effectors. We report here that TB/CYC (TEOSINTE-BRANCHED/CYCLOIDEA)-TCPs are destabilized by phytoplasma SAP11 effectors, leading to the proliferation of axillary meristems. Although a high degree of sequence diversity was observed among putative SAP11 effectors identified from evolutionarily distinct clusters of phytoplasmas, these effectors acquired fundamental activity in destabilizing TB/CYC-TCPs. In addition, we demonstrate that miR156/SPLs and miR172/AP2 modules, which represent key regulatory hubs involved in plant phase transition, were modulated by Aster Yellows phytoplasma strain Witches' Broom (AY-WB) protein SAP11. A late-flowering phenotype with significant changes in the expression of flowering-related genes was observed in transgenic Arabidopsis plants expressing SAP11AYWB. These morphological and molecular alterations were correlated with the ability of SAP11 effectors to destabilize CIN (CINCINNATA)-TCPs. Although not all putative SAP11 effectors display broad-spectrum activities in modulating morphological and physiological changes in host plants, they serve as core virulence factors responsible for the witches' broom symptom caused by phytoplasmas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / anatomy & histology
  • Arabidopsis / genetics*
  • Arabidopsis / metabolism
  • Arabidopsis / virology
  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Phytoplasma / genetics
  • Phytoplasma / physiology*
  • Plant Immunity / genetics
  • Plants, Genetically Modified / anatomy & histology
  • Plants, Genetically Modified / genetics
  • Plants, Genetically Modified / metabolism
  • Plants, Genetically Modified / virology
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Virulence Factors

Substances

  • Arabidopsis Proteins
  • MicroRNAs
  • TCP1 protein, Arabidopsis
  • TCP2 protein, Arabidopsis
  • Transcription Factors
  • Virulence Factors