The atypical histone variant H3.15 promotes callus formation in Arabidopsis thaliana

Development. 2020 Jun 3;147(11):dev184895. doi: 10.1242/dev.184895.

Abstract

Plants are capable of regenerating new organs after mechanical injury. The regeneration process involves genome-wide reprogramming of transcription, which usually requires dynamic changes in the chromatin landscape. We show that the histone 3 variant HISTONE THREE RELATED 15 (H3.15) plays an important role in cell fate reprogramming during plant regeneration in Arabidopsis H3.15 expression is rapidly induced upon wounding. Ectopic overexpression of H3.15 promotes cell proliferation to form a larger callus at the wound site, whereas htr15 mutation compromises callus formation. H3.15 is distinguished from other Arabidopsis histones by the absence of the lysine residue 27 that is trimethylated by the POLYCOMB REPRESSIVE COMPLEX 2 (PRC2) in constitutively expressed H3 variants. Overexpression of H3.15 promotes the removal of the transcriptional repressive mark H3K27me3 from chromatin, which results in transcriptional de-repression of downstream genes, such as WUSCHEL RELATED HOMEOBOX 11 (WOX11). Our results reveal a new mechanism for a release from PRC2-mediated gene repression through H3.15 deposition into chromatin, which is involved in reprogramming cell fate to produce pluripotent callus cells.

Keywords: Callus formation; Cell fate reprogramming; H3.15; H3K27me3; Regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / classification
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Chromatin / metabolism
  • Gene Expression Regulation, Plant
  • Histones / classification
  • Histones / genetics
  • Histones / metabolism*
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Methylation
  • Mutagenesis, Site-Directed
  • Phylogeny
  • Plants, Genetically Modified / metabolism
  • Polycomb Repressive Complex 2 / metabolism
  • Sequence Alignment
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Arabidopsis Proteins
  • Chromatin
  • Histones
  • Homeodomain Proteins
  • LBD18 protein, Arabidopsis
  • PRC2 protein, Arabidopsis
  • Transcription Factors
  • WOX11 protein, Arabidopsis
  • Polycomb Repressive Complex 2