BMP4 triggers regulatory circuits specifying the cardiac mesoderm lineage

Author:

Tsaytler Pavel1ORCID,Liu Jinhua1ORCID,Blaess Gaby1,Schifferl Dennis1ORCID,Veenvliet Jesse V.1ORCID,Wittler Lars1,Timmermann Bernd23,Herrmann Bernhard G.1ORCID,Koch Frederic1ORCID

Affiliation:

1. Max Planck Institute for Molecular Genetics 1 Department of Developmental Genetics , , 14195 Berlin , Germany

2. Sequencing Core Facility 2 , 14195 Berlin , Germany

3. Max Planck Institute for Molecular Genetics, 2 , 14195 Berlin , Germany

Abstract

ABSTRACT Cardiac lineage specification in the mouse is controlled by TGFβ and WNT signaling. From fly to fish, BMP has been identified as an indispensable heart inducer. A detailed analysis of the role of Bmp4 and its effectors Smad1/5, however, was still missing. We show that Bmp4 induces cardiac mesoderm formation in murine embryonic stem cells in vitro. Bmp4 first activates Wnt3 and upregulates Nodal. pSmad1/5 and the WNT effector Tcf3 form a complex, and together with pSmad2/3 activate mesoderm enhancers and Eomes. They then cooperate with Eomes to consolidate the expression of many mesoderm factors, including T. Eomes and T form a positive- feedback loop and open additional enhancers regulating early mesoderm genes, including the transcription factor Mesp1, establishing the cardiac mesoderm lineage. In parallel, the neural fate is suppressed. Our data confirm the pivotal role of Bmp4 in cardiac mesoderm formation in the mouse. We describe in detail the consecutive and cooperative actions of three signaling pathways, BMP, WNT and Nodal, and their effector transcription factors, during cardiac mesoderm specification.

Funder

Alexander von Humboldt-Stiftung

Max-Planck-Gesellschaft

Max Planck Society

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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