Blankenship J T, Wieschaus E
Howard Hughes Medical Institute, Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Development. 2001 Dec;128(24):5129-38. doi: 10.1242/dev.128.24.5129.
Although gastrulation is regarded as the stage during Drosophila development when the AP patterning system first influences morphological processes, transcription is regulated in complex patterns already at cycle 10. How soon this transcriptional complexity produces spatial differences in morphology has been unclear. We report on two new processes that establish visible morphological inhomogeneities before the onset of gastrulation. The first of these is the regulation of syncytial nuclear densities in the anterior end of the egg and represents the first zygotically driven AP asymmetry in the embryo. The second process is the generation of a fine-scale pattern in the actin/myosin array during cellularization. We find three domains of different yolk stalk diameters as well as depths of cellularization along the AP axis. These domains are established under the control of the AP patterning system and require bicoid activity. The anterior-most domain is a region of large yolk stalk diameters and corresponds to the region of decreased nuclear densities observed during syncytial stages. The middle domain shows smaller yolk stalk diameters and more rapid cellularization. Its establishment requires wild-type paired activity and thus indirectly requires bicoid. It occurs in a region of the embryo that ultimately gives rise to the cephalic furrow and may account for the effect of paired on that structure during gastrulation. Our results therefore suggest a link between cytoskeletal organization during cellularization and subsequent morphogenetic processes of gastrulation.
尽管原肠胚形成被视为果蝇发育过程中前后轴(AP)模式系统首次影响形态发生过程的阶段,但转录在第10个细胞周期时就已经以复杂的模式受到调控。这种转录复杂性在多早的时候会导致形态上的空间差异尚不清楚。我们报告了两个新过程,它们在原肠胚形成开始之前就建立了可见的形态不均匀性。其中第一个过程是对卵前端合胞体核密度的调控,这代表了胚胎中第一个由合子驱动的前后轴不对称性。第二个过程是在细胞化过程中肌动蛋白/肌球蛋白阵列中产生精细尺度的模式。我们沿着前后轴发现了三个不同卵黄柄直径以及细胞化深度的区域。这些区域是在前后轴模式系统的控制下建立的,并且需要双尾活性。最前端的区域是卵黄柄直径较大的区域,对应于在合胞体阶段观察到的核密度降低的区域。中间区域显示卵黄柄直径较小且细胞化更快。它的建立需要野生型配对活性,因此间接需要双尾。它出现在胚胎中最终形成头沟的区域,可能解释了配对在原肠胚形成期间对该结构的影响。因此,我们的结果表明细胞化过程中的细胞骨架组织与随后的原肠胚形成形态发生过程之间存在联系。