The chromatin-remodeling protein BAF60/SWP73A regulates the plant immune receptor NLRs

Cell Host Microbe. 2021 Mar 10;29(3):425-434.e4. doi: 10.1016/j.chom.2021.01.005. Epub 2021 Feb 5.

Abstract

In both plant and animal innate immune responses, surveillance of pathogen infection is mediated by membrane-associated receptors and intracellular nucleotide-binding domain and leucine-rich-repeat receptors (NLRs). Homeostasis of NLRs is under tight multilayered regulation to avoid over-accumulation or over-activation, which often leads to autoimmune responses that have detrimental effects on growth and development. How NLRs are regulated epigenetically at the chromatin level remains unclear. Here, we report that SWP73A, an ortholog of the mammalian switch/sucrose nonfermentable (SWI/SNF) chromatin-remodeling protein BAF60, suppresses the expression of NLRs either directly by binding to the NLR promoters or indirectly by affecting the alternative splicing of some NLRs through the suppression of cell division cycle 5 (CDC5), a key regulator of RNA splicing. Upon infection, bacteria-induced small RNAs silence SWP73A to activate a group of NLRs and trigger robust immune responses. SWP73A may function as a H3K9me2 reader to enhance transcription suppression.

Keywords: BAF60/SWP73; chromatin remodeling; epigenetic regulation; intracellular Nod-like receptors (NLRs); leucine-rich repeat receptors (NB-LRR receptors); nucleotide-binding domain; plant immunity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Arabidopsis Proteins / immunology
  • Cell Cycle Proteins / metabolism
  • Chromatin / metabolism*
  • Chromosomal Proteins, Non-Histone / immunology*
  • DNA-Binding Proteins / immunology*
  • Histones / metabolism
  • NLR Proteins / metabolism*
  • Plant Diseases / immunology
  • Plant Immunity*
  • Plant Proteins / metabolism
  • Plants
  • Protein Domains
  • Protein Serine-Threonine Kinases / metabolism
  • RNA Splicing
  • Receptors, Cell Surface / metabolism
  • Saccharomyces cerevisiae Proteins / metabolism
  • Signal Transduction
  • Transcription Factors

Substances

  • Arabidopsis Proteins
  • BAF60 protein, Arabidopsis
  • Cell Cycle Proteins
  • Chromatin
  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Histones
  • NLR Proteins
  • Plant Proteins
  • Receptors, Cell Surface
  • STRUWWELPETER protein, Arabidopsis
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Protein Serine-Threonine Kinases
  • CDC5 protein, S cerevisiae