Nakatani Y, Yasuo H, Satoh N, Nishida H
Department of Life Science, Tokyo Institute of Technology, Japan.
Development. 1996 Jul;122(7):2023-31. doi: 10.1242/dev.122.7.2023.
The tadpole larva of an ascidian develops 40 notochord cells in the center of its tail. Most of the notochord cells originate from the A-line precursors, among which inductive interactions are required for the subsequent differentiation of notochord. The presumptive-endoderm blastomeres or presumptive-notochord blastomeres themselves are inducers of notochord formation. Notochord induction takes place during the 32-cell stage. In amphibia, mesoderm induction is thought to be mediated by several growth factors, for example, activins and basic fibroblast growth factor (bFGF). In the ascidian, Halocynthia roretzi, treatment with bFGF of presumptive-notochord blastomeres that had been isolated at the early 32-cell stage promoted the formation of notochord at a low concentration of bFGF (0.02 ng/ml), while activin failed to induce notochord differentiation. The effect of bFGF reached a maximum at the end of the 32-cell stage and rapidly faded at the beginning of the subsequent cleavage, the time for full induction of notochord being at least 20 minutes. The expression of As-T, a previously isolated ascidian homolog of the mouse Brachyury (T) gene, starts at the 64-cell stage and is detectable exclusively in the presumptive-notochord blastomeres. The present study showed that presumptive-notochord blastomeres, isolated at the early 32-cell stage, neither differentiated into notochord nor expressed the As-T gene. However, when the presumptive-notochord blastomeres were coisolated or recombined with inducer blastomeres, transcripts of As-T were detected. When presumptive-notochord blastomeres were treated with bFGF, the expression of the As-T gene was also detected. These results suggest that inductive interaction is required for the expression of the As-T gene and that the expression of the As-T gene is closely correlated with the determined state of the notochord-precursor cells.
海鞘的蝌蚪幼虫在其尾部中央发育出40个脊索细胞。大多数脊索细胞起源于A系前体细胞,其中脊索后续分化需要诱导相互作用。预定内胚层卵裂球或预定脊索卵裂球自身是脊索形成的诱导物。脊索诱导发生在32细胞期。在两栖动物中,中胚层诱导被认为是由几种生长因子介导的,例如激活素和碱性成纤维细胞生长因子(bFGF)。在海鞘柄海鞘中,用bFGF处理在32细胞早期分离的预定脊索卵裂球,在低浓度bFGF(0.02 ng/ml)下促进了脊索的形成,而激活素未能诱导脊索分化。bFGF的作用在32细胞期末达到最大值,并在随后的卵裂开始时迅速消失,脊索完全诱导的时间至少为20分钟。As-T是先前分离的小鼠短尾(T)基因的海鞘同源物,其表达在64细胞期开始,并且仅在预定脊索卵裂球中可检测到。本研究表明,在32细胞早期分离的预定脊索卵裂球既不分化为脊索也不表达As-T基因。然而,当预定脊索卵裂球与诱导卵裂球共同分离或重组时,可检测到As-T的转录本。当预定脊索卵裂球用bFGF处理时,也检测到了As-T基因的表达。这些结果表明,诱导相互作用是As-T基因表达所必需的,并且As-T基因的表达与脊索前体细胞的确定状态密切相关。