一个驱动胚胎肌节中FGF4基因表达的保守增强子元件被GATA蛋白和bHLH蛋白协同激活。
A conserved enhancer element that drives FGF4 gene expression in the embryonic myotomes is synergistically activated by GATA and bHLH proteins.
作者信息
Iwahori Akiyo, Fraidenraich Diego, Basilico Claudio
机构信息
Department of Microbiology, New York University School of Medicine, New York, NY 10016, USA.
出版信息
Dev Biol. 2004 Jun 15;270(2):525-37. doi: 10.1016/j.ydbio.2004.03.012.
FGF4 is the earliest member of the fibroblast growth factor (FGF) family expressed during embryogenesis where it plays essential roles in post-implantation development and limb growth and patterning. The expression of the Fgf4 gene in specific developmental stages, including the ICM of the blastocyst, the myotomes, and the limb bud AER, is regulated by distinct enhancer elements (Hom) in the 3' UTR. We previously identified the Hom3a region as the major DNA element responsible for Fgf4 expression in the myotomes and AER, and showed that a conserved E-box is a target for the myogenic bHLH transcription factors MYF5 and MYOD. To further define the cis- and trans-acting elements that determine Hom3a activity, we conducted a mutational analysis of the ability of the Hom3a region to drive lacZ expression in the myotomes of transgenic mice. We identified a minimal enhancer of 226nt that contains four elements, including the E-box, necessary to drive gene expression in the myotomes. One of these elements is a binding site for the GATA family of transcription factors, and we show here that GATA 1-4 and 6 can synergize with MYF5 or MYOD to activate transcription of a reporter plasmid driven by a portion of the Hom3a enhancer including the GATA site and the E-box. In line with this finding, we could show a direct interaction between MYF5/MYOD and GATA-3 or GATA-4, mediated by the N-terminal and bHLH domains of MYF5/MYOD and the C-terminal zing finger domain of GATA-3/4. To further study the role of the Hom3a enhancer in directing Fgf4 expression and the function of FGF4 in limb and muscle development, we generated mutant mice in which the Fgf4 Hom3a region had been deleted (Delta3a). In situ hybridization analysis of sections from Delta3a/ Delta3a embryos at E11.5 showed a drastically reduced expression of Fgf4 mRNA in the myotomes and AER. However, these mice developed normally and show no limb or muscle defects, and the same was true of heterozygous mice in which one Fgf4 allele carried the Hom3a deletion and the other was a null allele (Delta3a/Fgf4(-)). Together, these results show that Hom3a is the major DNA enhancer element directing Fgf4 expression in myotomes and limb bud AER, and that its activity in the myotomes results at least in part from the synergistic action of GATA and bHLH myogenic factors that bind to evolutionary conserved sequences in the Hom3a enhancer. However, expression of Fgf4 in the myotomes or AER of murine embryos does not appear to be essential for muscle or limb development.
成纤维细胞生长因子4(FGF4)是成纤维细胞生长因子(FGF)家族中在胚胎发生过程中最早表达的成员,它在植入后发育以及肢体生长和模式形成中发挥着至关重要的作用。Fgf4基因在特定发育阶段的表达,包括囊胚的内细胞团、肌节和肢芽顶端外胚层嵴(AER),受3'非翻译区中不同的增强子元件(Hom)调控。我们之前鉴定出Hom3a区域是负责Fgf4在肌节和AER中表达的主要DNA元件,并表明一个保守的E盒是生肌bHLH转录因子MYF5和MYOD的作用靶点。为了进一步确定决定Hom3a活性的顺式和反式作用元件,我们对Hom3a区域驱动转基因小鼠肌节中lacZ表达的能力进行了突变分析。我们鉴定出一个226nt的最小增强子,它包含四个元件,包括在肌节中驱动基因表达所必需的E盒。这些元件之一是转录因子GATA家族的结合位点,我们在此表明GATA 1 - 4和6可以与MYF5或MYOD协同作用,激活由包含GATA位点和E盒的部分Hom3a增强子驱动的报告质粒的转录。与此发现一致,我们可以证明MYF5/MYOD与GATA - 3或GATA - 4之间存在直接相互作用,这种相互作用由MYF5/MYOD的N端和bHLH结构域以及GATA - 3/4的C端锌指结构域介导。为了进一步研究Hom3a增强子在指导Fgf4表达中的作用以及FGF4在肢体和肌肉发育中的功能,我们生成了Fgf4的Hom3a区域被删除的突变小鼠(Delta3a)。对E11.5的Delta3a/Delta3a胚胎切片进行原位杂交分析显示,Fgf4 mRNA在肌节和AER中的表达大幅降低。然而,这些小鼠发育正常,未表现出肢体或肌肉缺陷,携带一个Fgf4等位基因的Hom3a缺失且另一个为无效等位基因(Delta3a/Fgf4(-))的杂合小鼠也是如此。总之,这些结果表明Hom3a是指导Fgf4在肌节和肢芽AER中表达的主要DNA增强子元件,其在肌节中的活性至少部分源于与Hom3a增强子中进化保守序列结合的GATA和bHLH生肌因子的协同作用。然而,Fgf4在小鼠胚胎的肌节或AER中的表达似乎对肌肉或肢体发育并非必不可少。