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Genomic integration of Wnt/β-catenin and BMP/Smad1 signaling coordinates foregut and hindgut transcriptional programs

机译:Wnt /β-catenin和BMP / Smad1信号传导的基因组整合可协调前肠和后肠转录程序

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摘要

Digestive system development is orchestrated by combinatorial signaling interactions between endoderm and mesoderm, but how these signals are interpreted in the genome is poorly understood. Here we identified the transcriptomes of Xenopus foregut and hindgut progenitors, which are conserved with mammals. Using RNA-seq and ChIP-seq we show that BMP/Smad1 regulates dorsal-ventral gene expression in both the endoderm and mesoderm, whereas Wnt/β-catenin acts as a genome-wide toggle between foregut and hindgut programs. Unexpectedly, β-catenin and Smad1 binding were associated with both transcriptional activation and repression, with Wnt-repressed genes often lacking canonical Tcf DNA binding motifs, suggesting a novel mode of direct repression. Combinatorial Wnt and BMP signaling was mediated by Smad1 and β-catenin co-occupying hundreds of cis-regulatory DNA elements, and by a crosstalk whereby Wnt negatively regulates BMP ligand expression in the foregut. These results extend our understanding of gastrointestinal organogenesis and of how Wnt and BMP might coordinate genomic responses in other contexts.
机译:消化系统的发育是通过内胚层和中胚层之间的组合信号相互作用来协调的,但是人们对这些信号在基因组中的解释却知之甚少。在这里,我们确定了非洲爪蟾前足和后肠祖细胞的转录组,它们与哺乳动物是保守的。使用RNA-seq和ChIP-seq,我们显示BMP / Smad1调节内胚层和中胚层的背腹基因表达,而Wnt /β-catenin充当前肠和后肠程序之间的全基因组切换。出乎意料的是,β-catenin和Smad1的结合与转录激活和抑制都相关,Wnt抑制的基因通常缺乏规范的Tcf DNA结合基序,提示了直接抑制的新模式。 Smad1和β-catenin共同占据数百个顺式调控DNA元件,并通过串扰介导Wnt和BMP信号转导,由此Wnt负调节前肠中BMP配体的表达。这些结果扩展了我们对胃肠器官发生以及Wnt和BMP如何在其他情况下协调基因组反应的理解。

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