Institute of Molecular and Cell Biology (IMCB), A-STAR (Agency for Science, Technology and Research) , 61 Biopolis Drive, Proteos , Singapore 138673.
Biol Open. 2012 Aug 15;1(8):747-53. doi: 10.1242/bio.20121636. Epub 2012 Jun 26.
The yolk syncytial layer (YSL) performs multiple critical roles during zebrafish development. However, little is known about the cellular and molecular mechanisms that underlie the formation of this important extraembryonic structure. Here, we demonstrate by timelapse confocal microscopy of a transgenic line expressing membrane-targeted GFP that the YSL forms as a result of the absence of cytokinesis between daughter nuclei at the tenth mitotic division and the regression of pre-existing marginal cell membranes, thus converting the former margin of the blastoderm into a syncytium. We show that disruption of components of the cytoskeleton induces the formation of an expanded YSL, and identify Rock1 as the regulator of cytoskeletal dynamics that lead to YSL formation. Our results suggest that the YSL forms as a result of controlled cytokinesis failure in the marginal blastomeres, and Rock1 function is necessary for this process to occur. Uncovering the cellular and molecular mechanisms underlying zebrafish YSL formation offers significant insight into syncytial development in other tissues as well as in pathological conditions.
卵黄合胞层 (YSL) 在斑马鱼发育过程中发挥多种关键作用。然而,对于形成这种重要的胚胎外结构的细胞和分子机制知之甚少。在这里,我们通过对表达膜靶向 GFP 的转基因系进行延时共聚焦显微镜观察表明,YSL 的形成是由于在第十次有丝分裂分裂过程中,子细胞核之间没有胞质分裂,以及先前存在的边缘细胞膜退化,从而将胚胎的前边缘转化为合胞体。我们表明,细胞骨架成分的破坏会诱导 YSL 的形成,并且鉴定出 Rock1 是导致 YSL 形成的细胞骨架动力学的调节剂。我们的结果表明,YSL 的形成是由于边缘卵裂球中细胞有丝分裂的受控失败,而 Rock1 功能对于这个过程的发生是必要的。揭示斑马鱼 YSL 形成的细胞和分子机制为其他组织以及病理条件下的合胞体发育提供了重要的见解。