Author(s): Weidgang CE, Russell R, Tata PR, Khl SJ, Illing A, , Weidgang CE, Russell R, Tata PR, Khl SJ, Illing A, , Weidgang CE, Russell R, Tata PR, Khl SJ, Illing A, , Weidgang CE, Russell R, Tata PR, Khl SJ, Illing A,
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Abstract Cell-fate decisions and pluripotency are dependent on networks of key transcriptional regulators. Recent reports demonstrated additional functions of pluripotency-associated factors during early lineage commitment. The T-box transcription factor TBX3 has been implicated in regulating embryonic stem cell self-renewal and cardiogenesis. Here, we show that TBX3 is dynamically expressed during specification of the mesendoderm lineages in differentiating embryonic stem cells (ESCs) in vitro and in developing mouse and Xenopus embryos in vivo. Forced TBX3 expression in ESCs promotes mesendoderm specification by directly activating key lineage specification factors and indirectly by enhancing paracrine Nodal/Smad2 signaling. TBX3 loss-of-function analyses in the Xenopus underline its requirement for mesendoderm lineage commitment. Moreover, we uncovered a functional redundancy between TBX3 and Tbx2 during Xenopus gastrulation. Taken together, we define further facets of TBX3 actions and map TBX3 as an upstream regulator of the mesendoderm transcriptional program during gastrulation.
This article was published in Stem Cell Reports
and referenced in Journal of Cell Signaling