Takahashi H, Mitani Y, Satoh G, Satoh N
Department of Zoology, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.
Development. 1999 Sep;126(17):3725-34. doi: 10.1242/dev.126.17.3725.
The Brachyury genes of two divergent ascidians, As-T of Halocynthia roretzi and Ci-Bra of Ciona intestinalis, are expressed exclusively in notochord precursor cells. A previous study showed that the notochord-specific expression of Ci-Bra is controlled by a minimal promoter that is composed of three distinct regions: a region responsible for repression of expression in non-notochord mesoderm cells, a region for activation of expression in notochord cells, and a region for activation of expression in non-notochord mesoderm cells, distal to proximal to the transcription initiation site, respectively. We examined various deletion constructs of the As-T/lacZ fusion gene and demonstrate that a module between -289 and -250 bp of the 5'-flanking region is responsible for notochord-specific expression of the reporter gene. Gel-shift assays suggested the binding of nuclear protein(s) to this module. The 5'-flanking region of As-T contains a potential T-binding motif (-ACCTAGGT-) around -160 bp. Deletion of this motif from the p(-289)As-T/lacZ diminished the reporter gene expression. In addition, coinjection of p(-289)As-T/lacZ and synthetic As-T mRNA resulted in ectopic expression of lacZ in non-notochord cells, suggesting that the T-binding motif is responsible for autoactivation of the gene. These findings revealed striking differences between the minimal promoters of As-T and Ci-Bra so far revealed, with respect to their notochord-specific expression. Furthermore, reciprocal injections of reporter gene constructs, namely As-T/lacZ into Ciona eggs and Ci-Bra/lacZ into Halocynthia eggs, suggest alterations in the cis-regulatory elements and trans-activation factors that have occurred during evolution of the two ascidian species.
两种不同海鞘(柄海鞘的As-T和玻璃海鞘的Ci-Bra)的Brachyury基因仅在脊索前体细胞中表达。先前的一项研究表明,Ci-Bra的脊索特异性表达受一个最小启动子控制,该启动子由三个不同区域组成:一个负责抑制非脊索中胚层细胞表达的区域、一个负责激活脊索细胞中表达的区域以及一个负责激活非脊索中胚层细胞中表达的区域,它们分别位于转录起始位点的远端到近端。我们检测了As-T/lacZ融合基因的各种缺失构建体,并证明5'-侧翼区域中-289至-250 bp之间的一个模块负责报告基因的脊索特异性表达。凝胶迁移试验表明核蛋白与该模块结合。As-T的5'-侧翼区域在-160 bp左右包含一个潜在的T结合基序(-ACCTAGGT-)。从p(-289)As-T/lacZ中缺失该基序会降低报告基因的表达。此外,共注射p(-289)As-T/lacZ和合成的As-T mRNA会导致lacZ在非脊索细胞中异位表达,这表明T结合基序负责该基因的自激活。这些发现揭示了到目前为止所揭示的As-T和Ci-Bra最小启动子在脊索特异性表达方面的显著差异。此外,将报告基因构建体相互注射,即把As-T/lacZ注射到玻璃海鞘卵中,把Ci-Bra/lacZ注射到柄海鞘卵中,表明在这两种海鞘物种进化过程中发生了顺式调控元件和反式激活因子的改变。