Methyl-CpG binding protein MBD1 couples histone H3 methylation at lysine 9 by SETDB1 to DNA replication and chromatin assembly

Mol Cell. 2004 Aug 27;15(4):595-605. doi: 10.1016/j.molcel.2004.06.043.

Abstract

In mammals, heterochromatin is characterized by DNA methylation at CpG dinucleotides and methylation at lysine 9 of histone H3. It is currently unclear whether there is a coordinated transmission of these two epigenetic modifications through DNA replication. Here we show that the methyl-CpG binding protein MBD1 forms a stable complex with histone H3-K9 methylase SETDB1. Moreover, during DNA replication, MBD1 recruits SETDB1 to the large subunit of chromatin assembly factor CAF-1 to form an S phase-specific CAF-1/MBD1/SETDB1 complex that facilitates methylation of H3-K9 during replication-coupled chromatin assembly. In the absence of MBD1, H3-K9 methylation is lost at multiple genomic loci and results in activation of p53BP2 gene, normally repressed by MBD1 in HeLa cells. Our data suggest a model in which H3-K9 methylation by SETDB1 is dependent on MBD1 and is heritably maintained through DNA replication to support the formation of stable heterochromatin at methylated DNA.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Apoptosis Regulatory Proteins
  • Carrier Proteins / genetics
  • Chromatin Assembly and Disassembly*
  • CpG Islands
  • DNA Replication*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Gene Silencing
  • HeLa Cells
  • Histone-Lysine N-Methyltransferase
  • Histones / metabolism*
  • Humans
  • Lysine / metabolism*
  • Macromolecular Substances
  • Methylation
  • Models, Biological
  • Promoter Regions, Genetic
  • Protein Methyltransferases / metabolism*
  • Proteins / metabolism
  • RNA, Small Interfering / metabolism
  • S Phase
  • Transcription Factors
  • Two-Hybrid System Techniques

Substances

  • Apoptosis Regulatory Proteins
  • CNOT8 protein, human
  • Carrier Proteins
  • DNA-Binding Proteins
  • Histones
  • MBD1 protein, human
  • Macromolecular Substances
  • Proteins
  • RNA, Small Interfering
  • TP53BP2 protein, human
  • Transcription Factors
  • Protein Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • SETDB1 protein, human
  • Lysine