Interaction of the Chromatin Remodeling Protein hINO80 with DNA

PLoS One. 2016 Jul 18;11(7):e0159370. doi: 10.1371/journal.pone.0159370. eCollection 2016.

Abstract

The presence of a highly conserved DNA binding domain in INO80 subfamily predicted that INO80 directly interacts with DNA and we demonstrated its DNA binding activity in vitro. Here we report the consensus motif recognized by the DBINO domain identified by SELEX method and demonstrate the specific interaction of INO80 with the consensus motif. We show that INO80 significantly down regulates the reporter gene expression through its binding motif, and the repression is dependent on the presence of INO80 but not YY1 in the cell. The interaction is lost if specific residues within the consensus motif are altered. We identify a large number of potential target sites of INO80 in the human genome through in silico analysis that can grouped into three classes; sites that contain the recognition sequence for INO80 and YY1, only YY1 and only INO80. We demonstrate the binding of INO80 to a representative set of sites in HEK cells and the correlated repressive histone modifications around the binding motif. In the light of the role of INO80 in homeotic gene regulation in Drosophila as an Enhancer of trithorax and polycomb protein (ETP) that can modify the effect of both repressive complexes like polycomb as well as the activating complex like trithorax, it remains to be seen if INO80 can act as a recruiter of chromatin modifying complexes.

MeSH terms

  • ATPases Associated with Diverse Cellular Activities
  • Animals
  • Base Sequence
  • Binding Sites
  • Cell Nucleus / chemistry
  • Cell Nucleus / metabolism
  • Chromatin / chemistry*
  • Chromatin / metabolism
  • Chromatin Assembly and Disassembly
  • Cloning, Molecular
  • DNA / metabolism*
  • DNA Helicases / antagonists & inhibitors
  • DNA Helicases / genetics
  • DNA Helicases / metabolism*
  • DNA-Binding Proteins
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Gene Expression
  • HEK293 Cells
  • Histones / genetics
  • Histones / metabolism*
  • Humans
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • SELEX Aptamer Technique
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • YY1 Transcription Factor / genetics
  • YY1 Transcription Factor / metabolism*

Substances

  • Chromatin
  • DNA-Binding Proteins
  • Drosophila Proteins
  • Histones
  • INO80 protein, Drosophila
  • RNA, Small Interfering
  • Recombinant Fusion Proteins
  • Transcription Factors
  • YY1 Transcription Factor
  • YY1 protein, human
  • DNA
  • ATPases Associated with Diverse Cellular Activities
  • DNA Helicases
  • INO80 protein, human

Grants and funding

This work was supported by the Council for Scientific and Industrial Research, Government of India (CSIR, No. 60(0102)/12/EMR-II and EpiHeD: BSC0118/2012-17 to VB). SM, SB and SJ are supported by a fellowship from CSIR. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.