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Eomesodermin induces Mesp1 expression and cardiac differentiation from embryonic stem cells in the absence of Activin

机译:在没有激活素的情况下Eomesodermin诱导胚胎干细胞Mesp1表达和心脏分化

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摘要

The transcription factor Eomesodermin (Eomes) is involved in early embryonic patterning, but the range of cell fates that it controls as well as its mechanisms of action remain unclear. Here we show that transient expression of Eomes promotes cardiovascular fate during embryonic stem cell differentiation. Eomes also rapidly induces the expression of Mesp1, a key regulator of cardiovascular differentiation, and directly binds to regulatory sequences of Mesp1. Eomes effects are strikingly modulated by Activin signalling: high levels of Activin inhibit the promotion of cardiac mesoderm by Eomes, while they enhance Eomes-dependent endodermal specification. These results place Eomes upstream of the Mesp1-dependent programme of cardiogenesis, and at the intersection of mesodermal and endodermal specification, depending on the levels of Activin/Nodal signalling.
机译:转录因子Eomesodermin(Eomes)参与了早期胚胎的模式形成,但它控制的细胞命运范围及其作用机制仍不清楚。在这里,我们显示Eomes的瞬时表达促进胚胎干细胞分化过程中的心血管命运。 Eomes还迅速诱导Mesp1的表达,Mesp1是心血管分化的关键调节因子,并直接与Mesp1的调节序列结合。 Eomes的作用受到激活素信号的显着调节:高水平的激活素抑制Eomes对心脏中胚层的促进作用,同时又增强了Eomes依赖性的内胚层规格。这些结果将Eomes置于依赖Mesp1的心脏发生程序的上游,并位于中胚层和内胚层规格的交集处,具体取决于激活素/节点信号的水平。

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