Association of ORCA/LRWD1 with repressive histone methyl transferases mediates heterochromatin organization

Nucleus. 2015;6(6):435-41. doi: 10.1080/19491034.2015.1102814. Epub 2016 Jan 14.

Abstract

Heterochromatin mostly constitutes tightly packaged DNA, decorated with repressive histone marks, including histone H3 methylated at lysine 9, histone H4 methylated at lysine 20 and histone H3 methylated at lysine 27. Each of these marks is incorporated by specific histone lysine methyl transferases. While constitutive heterochromatin enriched with H3K9me3 and H4K20me3 occur within repetitive elements, including centromeres and telomeres, the facultative heterochromatin resides on the inactive X-chromosome and contains H3K27me3 mark. Origin recognition complex-associated (ORCA/LRWD1) protein is required for the initiation of DNA replication and also plays crucial roles in heterochromatin organization. ORCA associates with constitutive and facultative heterochromatin in human cells and binds to repressive histone marks. We demonstrate that ORCA binds to multiple repressive histone methyl transferases including G9a, GLP, Suv39h1 (H3K9me2/3), Suv420h1/h2 (H4K20me2/3) and EZH2 (H3K27me3). Removal of ORCA from human cells causes aberrations in the chromatin architecture. We propose that ORCA acts as a scaffold protein that enables the formation of multiple histone lysine methyltransferase complexes at heterochromatic sites thereby facilitating chromatin organization.

Keywords: ORCA/LRWD1; heterochromatin; histone methyl transferases; replication.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / chemistry
  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Cell Line, Tumor
  • Chromosomes, Human, X
  • DNA / chemistry
  • DNA / metabolism
  • DNA Methylation
  • Gene Silencing
  • Heterochromatin / chemistry
  • Heterochromatin / metabolism*
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase / metabolism*
  • Histones / chemistry
  • Histones / metabolism
  • Humans
  • Microtubule Proteins / chemistry
  • Microtubule Proteins / metabolism*
  • Models, Molecular
  • Protein Binding
  • Sequestosome-1 Protein

Substances

  • Adaptor Proteins, Signal Transducing
  • Heterochromatin
  • Histones
  • LRWD1 protein, human
  • Microtubule Proteins
  • SQSTM1 protein, human
  • Sequestosome-1 Protein
  • DNA
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase