Pivotal role of AtSUVH2 in heterochromatic histone methylation and gene silencing in Arabidopsis

EMBO J. 2005 Apr 6;24(7):1418-29. doi: 10.1038/sj.emboj.7600604. Epub 2005 Mar 17.

Abstract

SU(VAR)3-9 like histone methyltransferases control heterochromatic domains in eukaryotes. In Arabidopsis, 10 SUVH genes encode SU(VAR)3-9 homologues where SUVH1, SUVH2 and SUVH4 (KRYPTONITE) represent distinct subgroups of SUVH genes. Loss of SUVH1 and SUVH4 causes weak reduction of heterochromatic histone H3K9 dimethylation, whereas in SUVH2 null plants mono- and dimethyl H3K9, mono- and dimethyl H3K27, and monomethyl H4K20, the histone methylation marks of Arabidopsis heterochromatin are significantly reduced. Like animal SU(VAR)3-9 proteins SUVH2 displays strong dosage-dependent effects. Loss of function suppresses, whereas overexpression enhances, gene silencing, causes ectopic heterochromatization and significant growth defects. Furthermore, modification of transgene silencing by SUVH2 is partially transmitted to the offspring plants. This epigenetic stability correlates with heritable changes in DNA methylation. Mutational dissection of SUVH2 indicates an implication of its N-terminus and YDG domain in directing DNA methylation to target sequences, a prerequisite for consecutive histone methylation. Gene silencing by SUVH2 depends on MET1 and DDM1, but not CMT3. In Arabidopsis, SUVH2 with its histone H3K9 and H4K20 methylation activity has a central role in heterochromatic gene silencing.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agrobacterium tumefaciens
  • Arabidopsis / genetics
  • Arabidopsis / growth & development
  • Arabidopsis / physiology*
  • Arabidopsis / ultrastructure
  • Arabidopsis Proteins / metabolism
  • Base Sequence
  • Blotting, Western
  • Crosses, Genetic
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • DNA Mutational Analysis
  • DNA Primers
  • DNA-Binding Proteins / metabolism
  • Epigenesis, Genetic / physiology
  • Gene Silencing / physiology*
  • Genetic Vectors
  • Genotype
  • Heterochromatin / metabolism*
  • Histone-Lysine N-Methyltransferase / genetics
  • Histone-Lysine N-Methyltransferase / metabolism*
  • Histones / metabolism*
  • Immunohistochemistry
  • Luciferases
  • Methylation
  • Microscopy, Electron
  • Microscopy, Fluorescence
  • Molecular Sequence Data
  • Phylogeny
  • Sequence Analysis, DNA
  • Transcription Factors / metabolism
  • Transfection
  • Transgenes / genetics

Substances

  • Arabidopsis Proteins
  • DDM1 protein, Arabidopsis
  • DNA Primers
  • DNA-Binding Proteins
  • Heterochromatin
  • Histones
  • Transcription Factors
  • Luciferases
  • MET1 protein, Arabidopsis
  • DNA (Cytosine-5-)-Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • SUVH2 protein, Arabidopsis