Proteome-wide analysis in Saccharomyces cerevisiae identifies several PHD fingers as novel direct and selective binding modules of histone H3 methylated at either lysine 4 or lysine 36

J Biol Chem. 2007 Jan 26;282(4):2450-5. doi: 10.1074/jbc.C600286200. Epub 2006 Dec 1.

Abstract

The PHD finger motif is a signature chromatin-associated motif that is found throughout eukaryotic proteomes. Here we have determined the histone methyl-lysine binding activity of the PHD fingers present within the Saccharomyces cerevisiae proteome. We provide evidence on the genomic scale that PHD fingers constitute a general class of effector modules for histone H3 trimethylated at lysine 4 (H3K4me3) and histone H3 trimethylated at lysine 36 (H3K36me3). Structural modeling of PHD fingers demonstrates a conserved mechanism for recognizing the trimethyl moiety and provides insight into the molecular basis of affinity for the different methyl-histone ligands. Together, our study suggests that a common function for PHD fingers is to transduce methyl-lysine events and sheds light on how a single histone modification can be linked to multiple biological outcomes.

Publication types

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

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • DNA-Binding Proteins
  • Histones / metabolism*
  • Homeodomain Proteins* / chemistry
  • Homeodomain Proteins* / metabolism
  • Lysine
  • Methylation
  • Molecular Sequence Data
  • Protein Binding
  • Protein Structure, Tertiary
  • Proteome
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins* / chemistry
  • Saccharomyces cerevisiae Proteins* / metabolism

Substances

  • DNA-Binding Proteins
  • Histones
  • Homeodomain Proteins
  • Proteome
  • Saccharomyces cerevisiae Proteins
  • Lysine