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首页> 外文期刊>Development >Gata4 expression in lateral mesoderm is downstream of BMP4 and is activated directly by Forkhead and GATA transcription factors through a distal enhancer element.
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Gata4 expression in lateral mesoderm is downstream of BMP4 and is activated directly by Forkhead and GATA transcription factors through a distal enhancer element.

机译:Gata4在外侧中胚层的表达位于BMP4的下游,并通过远端增强子元件被Forkhead和GATA转录因子直接激活。

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摘要

The GATA family of zinc-finger transcription factors plays key roles in the specification and differentiation of multiple cell types during development. GATA4 is an early regulator of gene expression during the development of endoderm and mesoderm, and genetic studies in mice have demonstrated that GATA4 is required for embryonic development. Despite the importance of GATA4 in tissue specification and differentiation, the mechanisms by which Gata4 expression is activated and the transcription factor pathways upstream of GATA4 remain largely undefined. To identify transcriptional regulators of Gata4 in the mouse, we screened conserved noncoding sequences from the mouse Gata4 gene for enhancer activity in transgenic embryos. Here, we define the regulation of a distal enhancer element from Gata4 that is sufficient to direct expression throughout the lateral mesoderm, beginning at 7.5 days of mouse embryonic development. The activity of this enhancer is initially broad but eventually becomes restricted to the mesenchyme surrounding the liver. We demonstrate that the function of this enhancer in transgenic embryos is dependent upon highly conserved Forkhead and GATA transcription factor binding sites, which are bound by FOXF1 and GATA4, respectively. Furthermore, the activity of the Gata4 lateral mesoderm enhancer is attenuated by the BMP antagonist Noggin, and the enhancer is not activated in Bmp4-null embryos. Thus, these studies establish that Gata4 is a direct transcriptional target of Forkhead and GATA transcription factors in the lateral mesoderm, and demonstrate that Gata4 lateral mesoderm enhancer activation requires BMP4, supporting a model in which GATA4 serves as a downstream effector of BMP signaling in the lateral mesoderm.
机译:锌指转录因子的GATA家族在发育过程中多种细胞类型的规范和分化中起着关键作用。 GATA4是内胚层和中胚层发育过程中基因表达的早期调节剂,小鼠的遗传研究表明,GATA4是胚胎发育所必需的。尽管GATA4在组织规格和分化中很重要,但激活Gata4表达的机制和GATA4上游的转录因子途径仍很不确定。为了鉴定小鼠中Gata4的转录调节因子,我们从小鼠Gata4基因中筛选了保守的非编码序列,用于转基因胚胎中的增强子活性。在这里,我们定义了从Gata4开始的远端增强子元件的调控,该调控足以指导整个小鼠中胚层的表达,从小鼠胚胎发育的7.5天开始。这种增强剂的活性最初很广,但最终仅限于肝脏周围的间质。我们证明,这种增强子在转基因胚胎中的功能取决于高度保守的Forkhead和GATA转录因子结合位点,分别由FOXF1和GATA4结合。此外,BMP拮抗剂Noggin减弱了Gata4外侧中胚层增强子的活性,而该增强子在Bmp4无效的胚胎中没有被激活。因此,这些研究确定Gata4是外侧中胚层中Forkhead和GATA转录因子的直接转录靶标,并证明Gata4外侧中胚层增强子激活需要BMP4,从而支持了其中GATA4充当BMP信号传导下游效应子的模型。外侧中胚层。

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