Schnabel R, Hutter H, Moerman D, Schnabel H
MPI für Biochemie, Martinsried, Germany.
Dev Biol. 1997 Apr 15;184(2):234-65. doi: 10.1006/dbio.1997.8509.
Caenorhabditis elegans is renowned for its invariant embryogenesis. This pattern of development is in apparent contrast to other organisms from Drosophila to higher vertebrates. With the aid of a 4D microscope system (multifocal, time-lapse video recording system) which permits the extensive documentation and analysis of cell divisions, cell positions, and migrations in single embryos we have analyzed normal embryogenesis of C. elegans. The instrumentation reveals a naturally occurring variability in cell division timing, cell positioning, and cell-cell contacts which could not have been detected by the direct observation used earlier (Sulston et al., 1983, Dev. Biol. 100, 64-119). Embryos are very flexible and produce an essentially invariant premorphogenetic stage from variable earlier stages. An analysis of the distribution of the descendants of the early founder blastomeres at the premorphogenetic stage shows that these establish discrete regions in the embryo, a process involving a considerable amount of cell movement, which again varies in different embryos. Only cell fate assignment remains invariant. However, as shown earlier, this is not due to an autonomous invariant specification of cell fates but due to the fact that cell-cell interactions occur very early when the topology of blastomeres in the embryo is still sufficiently precise to ensure reproducible patterns of inductions. A new concept that founder blastomeres produce embryonic regions in the embryo can explain the striking complexity of the lineage per se and also the complicated asymmetric lineage patterns by which the bilateral symmetry of the embryo is established. Many cells, including bilateral homologs, were apparently chosen for a specific fate solely by their position in the embryo, irrespectively of the lineage descent by which the cells are created. We postulate that the production of regions by cell-cell interactions is the pivotal principle guiding the embryogenesis of C. elegans and that the embryogenesis of the worm follows the same basic principles as embryogenesis in other organisms.
秀丽隐杆线虫以其不变的胚胎发育过程而闻名。这种发育模式与从果蝇到高等脊椎动物的其他生物体形成了明显对比。借助4D显微镜系统(多焦点、延时视频记录系统),该系统允许对单个胚胎中的细胞分裂、细胞位置和迁移进行广泛记录和分析,我们分析了秀丽隐杆线虫的正常胚胎发育。该仪器揭示了细胞分裂时间、细胞定位和细胞间接触中自然存在的变异性,这是早期直接观察(Sulston等人,1983年,《发育生物学》100卷,64 - 119页)所无法检测到的。胚胎非常灵活,从可变的早期阶段产生一个基本不变的形态发生前期阶段。对形态发生前期阶段早期奠基性卵裂球后代分布的分析表明,这些后代在胚胎中建立了离散区域,这一过程涉及大量细胞运动,而不同胚胎中的这种运动又有所不同。只有细胞命运的分配保持不变。然而,如前所示,这并非由于细胞命运的自主不变指定,而是由于细胞间相互作用在胚胎中卵裂球的拓扑结构仍然足够精确以确保可重复的诱导模式时就很早就发生了。一个新的概念,即奠基性卵裂球在胚胎中产生胚胎区域,可以解释谱系本身惊人的复杂性以及通过其建立胚胎双侧对称性的复杂不对称谱系模式。许多细胞,包括双侧同源细胞,显然仅仅根据它们在胚胎中的位置就被选择了特定的命运,而与产生这些细胞的谱系血统无关。我们推测,通过细胞间相互作用产生区域是指导秀丽隐杆线虫胚胎发育的关键原则,并且线虫的胚胎发育遵循与其他生物体胚胎发育相同的基本原理。