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A Novel Mammal-Specific Three Partite Enhancer Element Regulates Node and Notochord-Specific Noto Expression

机译:一种新的哺乳动物特定三三方增强子元件调控对节点和脊索特异性表达诺托

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摘要

The vertebrate organizer and notochord have conserved, essential functions for embryonic development and patterning. The restricted expression of developmental regulators in these tissues is directed by specific cis-regulatory modules (CRMs) whose sequence conservation varies considerably. Some CRMs have been conserved throughout vertebrates and likely represent ancestral regulatory networks, while others have diverged beyond recognition but still function over a wide evolutionary range. Here we identify and characterize a mammalian-specific CRM required for node and notochord specific (NNC) expression of NOTO, a transcription factor essential for node morphogenesis, nodal cilia movement and establishment of laterality in mouse. A 523 bp enhancer region (NOCE) upstream the Noto promoter was necessary and sufficient for NNC expression from the endogenous Noto locus. Three subregions in NOCE together mediated full activity in vivo. Binding sites for known transcription factors in NOCE were functional in vitro but dispensable for NOCE activity in vivo. A FOXA2 site in combination with a novel motif was necessary for NOCE activity in vivo. Strikingly, syntenic regions in non-mammalian vertebrates showed no recognizable sequence similarities. In contrast to its activity in mouse NOCE did not drive NNC expression in transgenic fish. NOCE represents a novel, mammal-specific CRM required for the highly restricted Noto expression in the node and nascent notochord and thus regulates normal node development and function.
机译:脊椎动物的组织者和脊索动物具有保守的,对于胚胎发育和图案形成必不可少的功能。这些组织中发育调节剂的受限制表达是由特定的顺式调节模块(CRM)指导的,它们的序列保守性差异很大。有些CRM在整个脊椎动物中都得到了保存,可能代表着祖先的调节网络,而另一些CRM则已超出人们的认识,但仍在很宽的进化范围内发挥作用。在这里,我们确定并表征了NOTO的节点和脊索特定(NNC)表达所需的哺乳动物特异性CRM,NOT是节点形态发生,结节纤毛运动和小鼠侧向性建立所必需的转录因子。 Noto启动子上游需要一个523 bp的增强子区域(NOCE),对于从内源性Noto基因座表达NNC来说是必要和充分的。 NOCE中的三个子区域共同介导了体内的全部活性。 NOCE中已知转录因子的结合位点在体外具有功能,但对于体内NOCE活性却是必不可少的。 FOXA2位点与一个新的主题相结合是体内NOCE活性所必需的。令人惊讶的是,非哺乳动物脊椎动物的同音区域没有可识别的序列相似性。与其在小鼠中的活性相反,NOCE不会驱动转基因鱼中NNC的表达。 NOCE代表结节和新生脊索中高度受限的Noto表达所需的新型哺乳动物特异性CRM,因此可调节正常结节的发育和功能。

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