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Yolk syncytial layer formation is a failure of cytokinesis mediated by Rock1 function in the early zebrafish embryo

机译:卵黄合胞体层形成是早期斑马鱼胚胎中Rock1功能介导的胞质分裂失败

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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.
机译:卵黄合胞体层(YSL)在斑马鱼发育过程中起着多种关键作用。但是,对于这种重要的胚外结构形成的细胞和分子机制知之甚少。在这里,我们通过延时共聚焦显微镜证实了表达膜靶向GFP的转基因株系的YSL形成,这是由于第十个有丝分裂分裂的子核之间没有胞质分裂和先前存在的边缘细胞膜消退而形成的。胚盘的前缘变成合胞体。我们表明破坏细胞骨架的成分诱导形成扩展的YSL,并确定Rock1为导致YSL形成的细胞骨架动力学的调节剂。我们的结果表明,YSL的形成是边缘卵裂球中受控的胞质分裂失败的结果,Rock1功能对于该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深入了解其他组织以及病理状况中的合胞体发育提供了重要见识。

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