Kawamura Akinori, Ovara Hiroki, Ooka Yuko, Kinoshita Hirofumi, Hoshikawa Miki, Nakajo Kenji, Yokota Daisuke, Fujino Yuuri, Higashijima Shin-ichi, Takada Shinji, Yamasu Kyo
Division of Life Science, Graduate School of Science and Engineering, Saitama University, Shimo-Okubo, Sakura-ku, Saitama City, Saitama 338-8570, Japan.
Division of Life Science, Graduate School of Science and Engineering, Saitama University, Shimo-Okubo, Sakura-ku, Saitama City, Saitama 338-8570, Japan.
Dev Biol. 2016 Jan 15;409(2):543-54. doi: 10.1016/j.ydbio.2015.11.010. Epub 2015 Nov 17.
In vertebrates, the periodic formation of somites from the presomitic mesoderm (PSM) is driven by the molecular oscillator known as the segmentation clock. The hairy-related gene, hes6/her13.2, functions as a hub by dimerizing with other oscillators of the segmentation clock in zebrafish embryos. Although hes6 exhibits a posterior-anterior expression gradient in the posterior PSM with a peak at the tailbud, the detailed mechanisms underlying this unique expression pattern have not yet been clarified. By establishing several transgenic lines, we found that the transcriptional regulatory region downstream of hes6 in combination with the hes6 3'UTR recapitulates the endogenous gradient of hes6 mRNA expression. This downstream region, which we termed the PT enhancer, possessed several putative binding sites for the T-box and Ets transcription factors that were required for the regulatory activity. Indeed, the T-box transcription factor (Tbx16) and Ets transcription factor (Pea3) bound specifically to the putative binding sites and regulated the enhancer activity in zebrafish embryos. In addition, the 3'UTR of hes6 is required for recapitulation of the endogenous mRNA expression. Furthermore, the PT enhancer with the 3'UTR of hes6 responded to the inhibition of retinoic acid synthesis and fibroblast growth factor signaling in a manner similar to endogenous hes6. The results showed that transcriptional regulation by the T-box and Ets transcription factors, combined with the mRNA stability given by the 3'UTR, is responsible for the unique expression gradient of hes6 mRNA in the posterior PSM of zebrafish embryos.
在脊椎动物中,体节从原肠胚中胚层(PSM)周期性形成是由称为分割时钟的分子振荡器驱动的。毛发相关基因hes6/her13.2在斑马鱼胚胎中通过与分割时钟的其他振荡器二聚化而发挥枢纽作用。尽管hes6在后部PSM中呈现后 - 前表达梯度,在尾芽处达到峰值,但这种独特表达模式背后的详细机制尚未阐明。通过建立几个转基因品系,我们发现hes6下游的转录调控区域与hes6 3'UTR结合可重现hes6 mRNA表达的内源性梯度。我们将这个下游区域称为PT增强子,它具有几个T盒和Ets转录因子的假定结合位点,这些位点是调控活性所必需的。事实上,T盒转录因子(Tbx16)和Ets转录因子(Pea3)特异性结合到假定的结合位点并调节斑马鱼胚胎中的增强子活性。此外,hes6的3'UTR对于重现内源性mRNA表达是必需的。此外,带有hes6 3'UTR的PT增强子以类似于内源性hes6的方式对视黄酸合成和成纤维细胞生长因子信号传导的抑制作出反应。结果表明,T盒和Ets转录因子的转录调控,结合3'UTR赋予的mRNA稳定性,是斑马鱼胚胎后部PSM中hes6 mRNA独特表达梯度的原因。