Brachyury and SMAD signalling collaboratively orchestrate distinct mesoderm and endoderm gene regulatory networks in differentiating human embryonic stem cells
journal contributionposted on 21.07.2020, 11:31 by Tiago Faial, Andreia S Bernardo, Sasha Mendjan, Evangelia Diamanti, Daniel Ortmann, George E Gentsch, Victoria L Mascetti, Matthew WB Trotter, James C Smith, Roger A Pedersen
The transcription factor brachyury (T, BRA) is one of the first markers of gastrulation and lineage specification in vertebrates. Despite its wide use and importance in stem cell and developmental biology, its functional genomic targets in human cells are largely unknown. Here, we use differentiating human embryonic stem cells to study the role of BRA in activin A-induced endoderm and BMP4-induced mesoderm progenitors. We show that BRA has distinct genome-wide binding landscapes in these two cell populations, and that BRA interacts and collaborates with SMAD1 or SMAD2/3 signalling to regulate the expression of its target genes in a cell-specific manner. Importantly, by manipulating the levels of BRA in cells exposed to different signalling environments, we demonstrate that BRA is essential for mesoderm but not for endoderm formation. Together, our data illuminate the function of BRA in the context of human embryonic development and show that the regulatory role of BRA is context dependent. Our study reinforces the importance of analysing the functions of a transcription factor in different cellular and signalling environments.
Embryonic stem cellsGastrulationGene regulatory networksHumanSMADT-BOXAnimalsBone Morphogenetic Protein 4Cell LineEmbryonic Stem CellsEndodermFetal ProteinsGene Expression Regulation, DevelopmentalHumansMesodermMiceMice, TransgenicNeurogenesisSmad1 ProteinSmad2 ProteinSmad3 ProteinT-Box Domain ProteinsSmith U117597140AS-ack06 Biological Sciences11 Medical and Health Sciences