Houston Douglas W
Department of Biology, University of Iowa, Iowa City, IA, USA.
Wiley Interdiscip Rev Dev Biol. 2012 May-Jun;1(3):371-88. doi: 10.1002/wdev.29. Epub 2012 Jan 19.
In Xenopus eggs, fertilization initiates a rotational movement of the cortex relative to the cytoplasm, resulting in the transport of critical determinants to the future dorsal side of the embryo. Cortical rotation is mediated by microtubules, resulting in activation of the Wnt/β-catenin signaling pathway and expression of organizer genes on the dorsal side of the blastula. Similar cytoplasmic localizations resulting in β-catenin activation occur in many chordate embryos, suggesting a deeply conserved mechanism for patterning early embryos. This review summarizes the experimental evidence for the molecular basis of this model, focusing on recent maternal loss-of-function studies that shed light on two main unanswered questions: (1) what regulates microtubule assembly during cortical rotation and (2) how is Wnt/β-catenin signaling activated dorsally? In addition, as these processes depend on vegetally localized molecules in the oocyte, the mechanisms of RNA localization and novel roles for localized RNAs in axis formation are discussed. The work reviewed here provides a beginning framework for understanding the coupling of asymmetry in oogenesis with the establishment of asymmetry in the embryo.
在非洲爪蟾卵中,受精引发皮质相对于细胞质的旋转运动,导致关键决定因子运输到胚胎未来的背侧。皮质旋转由微管介导,导致Wnt/β-连环蛋白信号通路激活以及囊胚背侧组织者基因的表达。许多脊索动物胚胎中都会出现导致β-连环蛋白激活的类似细胞质定位,这表明早期胚胎模式形成存在深度保守机制。本综述总结了该模型分子基础的实验证据,重点关注近期的母体功能丧失研究,这些研究揭示了两个主要未解决的问题:(1)皮质旋转过程中微管组装受什么调节,以及(2)Wnt/β-连环蛋白信号通路如何在背侧被激活?此外,由于这些过程依赖于卵母细胞中植物性定位的分子,因此还讨论了RNA定位机制以及定位RNA在轴形成中的新作用。本文综述的工作为理解卵子发生中的不对称性与胚胎中不对称性建立之间的耦合提供了一个初步框架。