Swalla B J
University of California, Davis, Bodega Marine Laboratory, Bodega Bay, California 94923.
Microsc Res Tech. 1993 Nov 1;26(4):274-84. doi: 10.1002/jemt.1070260403.
Ascidian embryos are useful for examining how events that occur during fertilization and cleavage affect gastrulation because they gastrulate early in development, during the seventh cleavage. In ascidians, both dorsal-ventral and anterior-posterior axes are determined before first cleavage. The dorsal-ventral axis is fixed along the animal-vegetal axis of the fertilized egg following the first phase of ooplasmic segregation, perhaps due to determinants moved to the vegetal pole in concert with the myoplasm and plasma membrane components. The first ooplasmic movements appear to be driven by the actin network in the cortical myoplasm. The anterior-posterior axis becomes apparent after the second phase of ooplasmic segregation, when the cortical myoplasm becomes detached from the egg membrane, and moves to the posterior pole of the embryo. This movement is dependent on microtubules and has been attributed to the formation and movement of the sperm aster. A major component of the cortical myoplasm, p58, is co-localized along the microtubules emanating from the sperm aster. Gastrulation begins during the seventh cleavage with the invagination of the large endodermal cells at the vegetal pole of the embryo. The neural plate appears as a thickening of the epidermis on the dorsal side of the larva during the ninth cleavage; then the neural folds are formed, join, and close, elaborating the neural tube. Following neurulation, the tail is elongated as the neural tube and notochord cells intercalate at the midline of the embryo. Investigations using anural (tailless) ascidian larvae suggest that some of the processes underlying elongation can be restored by the zygotic genome. Although ascidian larvae contain fewer cells and cell types than vertebrate embryos, ascidian gastrulation and morphogenesis appear to employ similar mechanisms to those in vertebrate embryos. The extent of our current knowledge about the mechanisms involved in gastrulation and tail formation is summarized, and further experiments are suggested to explore the molecular mechanisms underlying these processes.
海鞘胚胎对于研究受精和卵裂过程中发生的事件如何影响原肠胚形成很有用,因为它们在发育早期,即第七次卵裂时就开始原肠胚形成。在海鞘中,背腹轴和前后轴在第一次卵裂之前就已确定。背腹轴在卵质分离的第一阶段后,沿着受精卵的动物-植物轴固定,这可能是由于决定因子与肌质和质膜成分一起移动到植物极。第一次卵质运动似乎是由皮质肌质中的肌动蛋白网络驱动的。在卵质分离的第二阶段后,前后轴变得明显,此时皮质肌质与卵膜分离,并移动到胚胎的后极。这种运动依赖于微管,并归因于精子星体的形成和移动。皮质肌质的一个主要成分p58,沿着从精子星体发出的微管共定位。原肠胚形成在第七次卵裂时开始,胚胎植物极的大的内胚层细胞内陷。在第九次卵裂时,神经板在幼虫背侧的表皮处增厚出现;然后形成神经褶,合并并闭合,形成神经管。神经胚形成后,随着神经管和脊索细胞在胚胎中线处插入,尾巴伸长。使用无尾海鞘幼虫的研究表明,伸长的一些潜在过程可以由合子基因组恢复。尽管海鞘幼虫比脊椎动物胚胎包含的细胞和细胞类型更少,但海鞘的原肠胚形成和形态发生似乎采用了与脊椎动物胚胎相似的机制。总结了我们目前对原肠胚形成和尾巴形成所涉及机制的了解程度,并提出了进一步的实验来探索这些过程的分子机制。