Combined genomic and proteomic approaches reveal DNA binding sites and interaction partners of TBX2 in the developing lung

Respir Res. 2021 Mar 17;22(1):85. doi: 10.1186/s12931-021-01679-y.

Abstract

Background: Tbx2 encodes a transcriptional repressor implicated in the development of numerous organs in mouse. During lung development TBX2 maintains the proliferation of mesenchymal progenitors, and hence, epithelial proliferation and branching morphogenesis. The pro-proliferative function was traced to direct repression of the cell-cycle inhibitor genes Cdkn1a and Cdkn1b, as well as of genes encoding WNT antagonists, Frzb and Shisa3, to increase pro-proliferative WNT signaling. Despite these important molecular insights, we still lack knowledge of the DNA occupancy of TBX2 in the genome, and of the protein interaction partners involved in transcriptional repression of target genes.

Methods: We used chromatin immunoprecipitation (ChIP)-sequencing and expression analyses to identify genomic DNA-binding sites and transcription units directly regulated by TBX2 in the developing lung. Moreover, we purified TBX2 containing protein complexes from embryonic lung tissue and identified potential interaction partners by subsequent liquid chromatography/mass spectrometry. The interaction with candidate proteins was validated by immunofluorescence, proximity ligation and individual co-immunoprecipitation analyses.

Results: We identified Il33 and Ccn4 as additional direct target genes of TBX2 in the pulmonary mesenchyme. Analyzing TBX2 occupancy data unveiled the enrichment of five consensus sequences, three of which match T-box binding elements. The remaining two correspond to a high mobility group (HMG)-box and a homeobox consensus sequence motif. We found and validated binding of TBX2 to the HMG-box transcription factor HMGB2 and the homeobox transcription factor PBX1, to the heterochromatin protein CBX3, and to various members of the nucleosome remodeling and deacetylase (NuRD) chromatin remodeling complex including HDAC1, HDAC2 and CHD4.

Conclusion: Our data suggest that TBX2 interacts with homeobox and HMG-box transcription factors as well as with the NuRD chromatin remodeling complex to repress transcription of anti-proliferative genes in the pulmonary mesenchyme.

Keywords: CBX3; HDAC; HMGB2; Lung development; NuRD; PBX1; Pulmonary mesenchyme; Tbx2.

MeSH terms

  • Animals
  • Binding Sites
  • CCN Intercellular Signaling Proteins / genetics
  • CCN Intercellular Signaling Proteins / metabolism
  • Cell Proliferation
  • Chromatin Immunoprecipitation Sequencing
  • Chromatography, Liquid
  • Chromosomal Proteins, Non-Histone / genetics
  • Chromosomal Proteins, Non-Histone / metabolism
  • Fluorescent Antibody Technique
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental*
  • Genomics*
  • HEK293 Cells
  • HMGB2 Protein / genetics
  • HMGB2 Protein / metabolism
  • Humans
  • Interleukin-33 / genetics
  • Interleukin-33 / metabolism
  • Lung / embryology
  • Lung / metabolism*
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex / genetics
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex / metabolism
  • Mice
  • Mice, Knockout
  • Oligonucleotide Array Sequence Analysis
  • Polymerase Chain Reaction
  • Pre-B-Cell Leukemia Transcription Factor 1 / genetics
  • Pre-B-Cell Leukemia Transcription Factor 1 / metabolism
  • Proteomics*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Spectrometry, Mass, Electrospray Ionization
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism*
  • Tandem Mass Spectrometry

Substances

  • CCN Intercellular Signaling Proteins
  • CCN4 protein, mouse
  • Cbx3 protein, mouse
  • Chromosomal Proteins, Non-Histone
  • HMGB2 Protein
  • Il33 protein, mouse
  • Interleukin-33
  • Pbx1 protein, mouse
  • Pre-B-Cell Leukemia Transcription Factor 1
  • Proto-Oncogene Proteins
  • T-Box Domain Protein 2
  • T-Box Domain Proteins
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex