Nam Jongmin, Su Yi-Hsien, Lee Pei Yun, Robertson Anthony J, Coffman James A, Davidson Eric H
Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA.
Dev Biol. 2007 Jun 15;306(2):860-9. doi: 10.1016/j.ydbio.2007.03.033. Epub 2007 Mar 28.
Expression of the nodal gene initiates the gene regulatory network which establishes the transcriptional specification of the oral ectoderm in the sea urchin embryo. This gene encodes a TGFbeta ligand, and in Strongylocentrotus purpuratus its transcription is activated in the presumptive oral ectoderm at about the 30-cell stage. Thereafter Nodal signaling occurs among all cells of the oral ectoderm territory, and nodal expression is required for expression of oral ectoderm regulatory genes. The cis-regulatory system of the nodal gene transduces anisotropically distributed cytoplasmic cues that distinguish the future oral and aboral domains of the early embryo. Here we establish the genomic basis for the initiation and maintenance of nodal gene expression in the oral ectoderm. Functional cis-regulatory control modules of the nodal gene were identified by interspecific sequence conservation. A 5' cis-regulatory module functions both to initiate expression of the nodal gene and to maintain its expression by means of feedback input from the Nodal signal transduction system. These functions are mediated respectively by target sites for bZIP transcription factors, and by SMAD target sites. At least one SMAD site is also needed for the initiation of expression. An intron module also contains SMAD sites which respond to Nodal feedback, and in addition acts to repress vegetal expression. These observations explain the main features of nodal expression in the oral ectoderm: since the activity of bZIP factors is redox sensitive, and the initial polarization of oral vs. aboral fate is manifested in a redox differential, the bZIP sites account for the activation of nodal on the oral side; and since the immediate early signal transduction response factors for Nodal are SMAD factors, the SMAD sites account for the feedback maintenance of nodal gene expression.
结节基因的表达启动了基因调控网络,该网络确立了海胆胚胎口腔外胚层的转录特化。该基因编码一种转化生长因子β配体,在紫海胆中,其转录在约30细胞期的预定口腔外胚层中被激活。此后,结节信号在口腔外胚层区域的所有细胞之间发生,并且口腔外胚层调控基因的表达需要结节基因的表达。结节基因的顺式调控系统转导各向异性分布的细胞质信号,这些信号区分了早期胚胎未来的口腔和反口区域。在这里,我们确立了口腔外胚层中结节基因表达起始和维持的基因组基础。通过种间序列保守性鉴定出结节基因的功能性顺式调控控制模块。一个5'顺式调控模块既起到启动结节基因表达的作用,又通过来自结节信号转导系统的反馈输入来维持其表达。这些功能分别由碱性亮氨酸拉链转录因子的靶位点以及SMAD靶位点介导。表达起始还至少需要一个SMAD位点。一个内含子模块也包含对结节反馈有反应的SMAD位点,此外还起到抑制植物极表达的作用。这些观察结果解释了口腔外胚层中结节基因表达的主要特征:由于碱性亮氨酸拉链因子的活性对氧化还原敏感,并且口腔与反口命运的初始极化表现为氧化还原差异,碱性亮氨酸拉链位点解释了口腔侧结节基因的激活;并且由于结节的即时早期信号转导反应因子是SMAD因子,SMAD位点解释了结节基因表达的反馈维持。