Imai Kaoru S, Satou Yutaka, Satoh Nori
Department of Zoology, Graduate School of Science, Kyoto University, Sakyo-ku, 606-8502, Japan.
Development. 2002 Jun;129(11):2723-32. doi: 10.1242/dev.129.11.2723.
Multiple functions of a Zic-like zinc finger transcription factor gene (Cs-ZicL) were identified in Ciona savignyi embryos. cDNA clones for Cs-ZicL, a beta-catenin downstream genes, were isolated and the gene was transiently expressed in the A-line notochord/nerve cord lineage and in B-line muscle lineage from the 32-cell stage and later in a-line CNS lineage from the 110-cell stage. Suppression of Cs-ZicL function with specific morpholino oligonucleotide indicated that Cs-ZicL is essential for the formation of A-line notochord cells but not of B-line notochord cells, essential for the CNS formation and essential for the maintenance of muscle differentiation. The expression of Cs-ZicL in the A-line cells is downstream of beta-catenin and a beta-catenin-target gene, Cs-FoxD, which is expressed in the endoderm cells from the 16-cell stage and is essential for the differentiation of notochord. In spite of its pivotal role in muscle specification, the expression of Cs-ZicL in the muscle precursors is independent of Cs-macho1, which is another Zic-like gene encoding a Ciona maternal muscle determinant, suggesting another genetic cascade for muscle specification independent of Cs-macho1. Cs-ZicL may provide a future experimental system to explore how the gene expression in multiple embryonic regions is controlled and how the single gene can perform different functions in multiple types of embryonic cells.
在玻璃海鞘胚胎中鉴定出一种类Zic锌指转录因子基因(Cs-ZicL)的多种功能。分离出了作为β-连环蛋白下游基因的Cs-ZicL的cDNA克隆,该基因从32细胞期开始在A线脊索/神经索谱系以及B线肌肉谱系中瞬时表达,从110细胞期开始在A线中枢神经系统谱系中表达。用特异性吗啉代寡核苷酸抑制Cs-ZicL功能表明,Cs-ZicL对A线脊索细胞的形成至关重要,但对B线脊索细胞的形成并非必需,对中枢神经系统的形成至关重要,对肌肉分化的维持也至关重要。Cs-ZicL在A线细胞中的表达位于β-连环蛋白和一个β-连环蛋白靶基因Cs-FoxD的下游,Cs-FoxD从16细胞期开始在内胚层细胞中表达,对脊索的分化至关重要。尽管Cs-ZicL在肌肉特化中起关键作用,但其在肌肉前体细胞中的表达独立于Cs-macho1,Cs-macho1是另一个编码玻璃海鞘母体肌肉决定因子的类Zic基因,这表明存在另一个独立于Cs-macho1的肌肉特化遗传级联反应。Cs-ZicL可能为探索如何控制多个胚胎区域中的基因表达以及单个基因如何在多种类型的胚胎细胞中发挥不同功能提供一个未来的实验系统。