Kobayashi Akiko, Akasaka Koji, Kawaichi Masashi, Kokubo Tetsuro
Division of Gene Function in Animals, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.
Nucleic Acids Res. 2002 Jul 15;30(14):3034-44. doi: 10.1093/nar/gkf439.
The orthodenticle-related protein (HpOtx) gene derived from the sea urchin Hemicentrotus pulcherrimus encodes two distinct isoforms, HpOtxE and HpOtxL, which are differentially expressed during early embryogenesis and are driven by TATA-less and TATA-containing promoters, respectively. In order to determine if the TATA element is involved in the establishment of the temporally specific expression profile of the HpOtx gene, reporter genes under the control of modified or wild-type HpOtxE/L promoters were introduced into fertilized eggs. When the activities of the different promoter constructs were examined, we found that deletion of the TATA element from the HpOtxL promoter causes early expression, whereas addition of the TATA element to the HpOtxE promoter causes delayed expression. This suppressive action of the TATA element on transcription from the HpOtxE/L promoters requires the presence of upstream CACGTG elements. These results indicate that the presence or absence of the TATA element determines, at least in part, the expression profile of the HpOtxE/L promoters, in concert with the transcription factor(s) that binds to the upstream CACGTG element. Immunoblot and gel retardation analyses suggest that functional interaction between CACGTG binding factor(s) and TATA factor(s) may be regulated by an unidentified third factor(s) during early embryogenesis in the sea urchin.
源自海胆马粪海胆的正齿相关蛋白(HpOtx)基因编码两种不同的异构体,即HpOtxE和HpOtxL,它们在胚胎早期发育过程中差异表达,分别由无TATA盒和含TATA盒的启动子驱动。为了确定TATA元件是否参与HpOtx基因时间特异性表达谱的建立,将经修饰的或野生型HpOtxE/L启动子控制下的报告基因导入受精卵。当检测不同启动子构建体的活性时,我们发现从HpOtxL启动子中删除TATA元件会导致早期表达,而向HpOtxE启动子中添加TATA元件会导致表达延迟。TATA元件对HpOtxE/L启动子转录的这种抑制作用需要上游CACGTG元件的存在。这些结果表明,TATA元件的存在与否至少部分地决定了HpOtxE/L启动子的表达谱,这与结合上游CACGTG元件的转录因子协同作用。免疫印迹和凝胶阻滞分析表明,在海胆胚胎早期发育过程中,CACGTG结合因子与TATA因子之间的功能相互作用可能受一种未知的第三因子调控。