Martin E L, Consales C, Davidson E H, Arnone M I
Division of Biology, California Institute of Technology, Pasadena, California 91125, USA.
Dev Biol. 2001 Aug 1;236(1):46-63. doi: 10.1006/dbio.2001.0285.
The CyIIa gene of the sea urchin embryo is a model for study of cis-regulation downstream of cell-type specification, as CyIIa transcription follows the specification and initial differentiation of the embryonic domains in which it is expressed. These are the skeletogenic and secondary mesenchyme and gut. We carried out a detailed structural and functional analysis of a cis-regulatory region of this gene, extending 780 bp upstream and 125 bp downstream of the transcription start site, that had been shown earlier to reproduce faithfully the complex and dynamic CyIIa pattern of expression. This analysis revealed that the overall pattern of expression of the CyIIa gene appears to be governed mainly by two independent sets of DNA elements, which are target sites for specific proteins present in blastula-stage nuclear extract. One type of element, which controls a dynamic program of expression in both skeletogenic and secondary mesenchyme cells, contains the consensus-binding site for a member of the ets transcription factor family. The other, which is responsible for the terminal or permanent phase of CyIIa expression in the gut, shares homologies with the late module of the endoderm-specific Endo16 gene (endo16 Module B). Oligonucleotides containing replicas of these two target sites fused upstream of a sea urchin basal promoter are sufficient to confer accurate mesenchyme and late gut expression of an injected GFP construct. The finding of a single protein target site that recapitulates CyIIa expression in both primary and secondary mesenchyme cells suggests the existence of a pan-mesodermal gene expression program in the sea urchin embryo.
海胆胚胎的CyIIa基因是研究细胞类型特化下游顺式调控的模型,因为CyIIa转录遵循其表达所在胚胎区域的特化和初始分化过程。这些区域是造骨细胞、次生间充质细胞和肠道。我们对该基因的一个顺式调控区域进行了详细的结构和功能分析,该区域在转录起始位点上游延伸780 bp,下游延伸125 bp,先前已证明其能忠实地重现复杂且动态的CyIIa表达模式。该分析表明,CyIIa基因的整体表达模式似乎主要由两组独立的DNA元件控制,它们是囊胚期核提取物中存在的特定蛋白质的靶位点。一种元件控制造骨细胞和次生间充质细胞中的动态表达程序,包含ets转录因子家族成员的共有结合位点。另一种元件负责CyIIa在肠道中的终末或永久表达阶段,与内胚层特异性Endo16基因的晚期模块(endo16模块B)具有同源性。含有这两个靶位点复制品的寡核苷酸与海胆基础启动子上游融合,足以使注射的绿色荧光蛋白构建体在间充质细胞和晚期肠道中准确表达。在初级和次级间充质细胞中均能重现CyIIa表达的单个蛋白质靶位点的发现,表明海胆胚胎中存在一个泛中胚层基因表达程序。