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The Cardiac TBX5 Interactome Reveals a Chromatin Remodeling Network Essential for Cardiac Septation.

Lauren Waldron | Jeffrey D Steimle | Todd M Greco | Nicholas C Gomez | Kerry M Dorr | Junghun Kweon | Brenda Temple | Xinan Holly Yang | Caralynn M Wilczewski | Ian J Davis | Ileana M Cristea | Ivan P Moskowitz | Frank L Conlon
Developmental cell | 2016

Human mutations in the cardiac transcription factor gene TBX5 cause congenital heart disease (CHD), although the underlying mechanism is unknown. We report characterization of the endogenous TBX5 cardiac interactome and demonstrate that TBX5, long considered a transcriptional activator, interacts biochemically and genetically with the nucleosome remodeling and deacetylase (NuRD) repressor complex. Incompatible gene programs are repressed by TBX5 in the developing heart. CHD mis-sense mutations that disrupt the TBX5-NuRD interaction cause depression of a subset of repressed genes. Furthermore, the TBX5-NuRD interaction is required for heart development. Phylogenetic analysis showed that the TBX5-NuRD interaction domain evolved during early diversification of vertebrates, simultaneous with the evolution of cardiac septation. Collectively, this work defines a TBX5-NuRD interaction essential to cardiac development and the evolution of the mammalian heart, and when altered may contribute to human CHD.

Pubmed ID: 26859351

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: PHS HHS, United States
    Id: NIH/NIGMS R01 GM114141
  • Agency: NCI NIH HHS, United States
    Id: R21CA167305
  • Agency: NCI NIH HHS, United States
    Id: R21 CA167305
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL112618
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007092
  • Agency: American Heart Association-American Stroke Association, United States
    Id: 11PRE6110002
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL124836
  • Agency: NHLBI NIH HHS, United States
    Id: HL127640
  • Agency: NHLBI NIH HHS, United States
    Id: R01HL124836
  • Agency: NHLBI NIH HHS, United States
    Id: NIH RO1HL112618
  • Agency: NCI NIH HHS, United States
    Id: P30 CA016086
  • Agency: NIH HHS, United States
    Id: S10 OD018495
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL007381
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM114141
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL127640
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL092153
  • Agency: NIH HHS, United States
    Id: 1S10OD018495-01
  • Agency: NIGMS NIH HHS, United States
    Id: NIH T32 GM007183
  • Agency: NIGMS NIH HHS, United States
    Id: 5T32 GM007092
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL069768
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007183
  • Agency: NIH HHS, United States
    Id: P40 OD010997

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Cytoscape (tool)

RRID:SCR_003032

Software platform for complex network analysis and visualization. Used for visualization of molecular interaction networks and biological pathways and integrating these networks with annotations, gene expression profiles and other state data.

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HHpred (tool)

RRID:SCR_010276

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KEGG (tool)

RRID:SCR_012773

Integrated database resource consisting of 16 main databases, broadly categorized into systems information, genomic information, and chemical information. In particular, gene catalogs in completely sequenced genomes are linked to higher-level systemic functions of cell, organism, and ecosystem. Analysis tools are also available. KEGG may be used as reference knowledge base for biological interpretation of large-scale datasets generated by sequencing and other high-throughput experimental technologies.

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RRID:SCR_013731

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