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Foxd3 suppresses NFAT-mediated differentiation to maintain self-renewal of embryonic stem cells

机译:Foxd3抑制NFAT介导的分化,以维持胚胎干细胞的自我更新

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摘要

Pluripotency-associated transcription factor Foxd3 is required for maintaining pluripotent cells. However, molecular mechanisms underlying its function are largely unknown. Here, we report that Foxd3 suppresses differentiation induced by calcineurin-NFAT signaling to maintain the ESC identity. Mechanistically, Foxd3 interacts with NFAT proteins and recruits co-repressor Tle4, a member of the Tle repressor family highly expressed in undifferentiated ESCs, to suppress NFATc3's transcriptional activities. Furthermore, global transcriptome analysis shows that Foxd3 and NFATc3 co-regulate a set of differentiation-associated genes in ESCs. Collectively, our study establishes a molecular and functional link between a pluripotency-associated factor and an important ESC differentiation-inducing pathway.
机译:多能性相关转录因子Foxd3是维持多能细胞所必需的。但是,其功能的分子机制在很大程度上尚不清楚。在这里,我们报告Foxd3抑制钙调神经磷酸酶NFAT信号诱导的分化,以维持ESC身份。从机制上讲,Foxd3与NFAT蛋白质相互作用,并募集共抑制子Tle4(Tle抑制子家族的成员,在未分化的ESC中高度表达),以抑制NFATc3的转录活性。此外,全局转录组分析显示Foxd3和NFATc3共同调节ESC中的一组分化相关基因。总的来说,我们的研究建立了多能性相关因子与重要的ESC分化诱导途径之间的分子和功能联系。

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