Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305-5174, USA.
Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305-5174, USA; Laboratory of Dynamics in Biological Systems, KU Leuven, Department of Cellular and Molecular Medicine, University of Leuven, 3000 Leuven, Belgium; Applied Physics Research Group, Vrije Universiteit Brussel (VUB), 1050 Brussels, Belgium.
Cell Rep. 2017 Oct 3;21(1):37-46. doi: 10.1016/j.celrep.2017.09.017.
The early Xenopus laevis embryo is replete with dynamic spatial waves. One such wave, the cell division wave, emerges from the collective cell division timing of first tens and later hundreds of cells throughout the embryo. Here, we show that cell division waves do not propagate between neighboring cells and do not rely on cell-to-cell coupling to maintain their division timing. Instead, intrinsic variation in division period autonomously and gradually builds these striking patterns of cell division. Disrupting this pattern of division by placing embryos in a temperature gradient resulted in highly asynchronous entry to the midblastula transition and misexpression of the mesodermal marker Xbra. Remarkably, this gene expression defect is corrected during involution, resulting in delayed yet normal Xbra expression and viable embryos. This implies the existence of a previously unknown mechanism for normalizing mesodermal gene expression during involution.
非洲爪蟾早期胚胎中充满了动态的空间波。其中一种波,即细胞分裂波,是由胚胎中最初数十个,后来数百个细胞的集体细胞分裂时间产生的。在这里,我们表明细胞分裂波不会在相邻细胞之间传播,也不依赖于细胞间的偶联来维持它们的分裂时间。相反,分裂周期的内在变化自主且逐渐构建了这些显著的细胞分裂模式。通过将胚胎置于温度梯度中来破坏这种分裂模式,导致高度异步进入中囊胚转换,并导致中胚层标记物 Xbra 的错误表达。值得注意的是,在卷入过程中,这种基因表达缺陷得到了纠正,导致 Xbra 的表达延迟但正常,并且胚胎存活。这意味着在卷入过程中存在一种以前未知的正常化中胚层基因表达的机制。