Department of Biomedical Sciences, Florida State University College of Medicine, Tallahassee, FL 32306, USA.
Cell Mol Life Sci. 2011 Aug;68(15):2555-67. doi: 10.1007/s00018-011-0695-5. Epub 2011 May 5.
The establishment of left-right (LR) asymmetry is regulated by intricate signaling mechanisms during embryogenesis and this asymmetry is critical for morphogenesis as well as the positioning of internal organs within the organism. Recent progress including elucidation of ion transporters, leftward nodal flow, and regulation of asymmetric gene expression contributes to our understanding of how the breaking of the symmetry is initiated and how this laterality information is subsequently transmitted to the organ primordium. A number of developmental signaling pathways have been implicated in this complex process. In this review, we will focus on the roles of the Notch signaling pathway during development of LR asymmetry. The Notch signaling pathway is a short-range communication system between neighboring cells. While Notch signaling plays essential roles in regulating the morphogenesis of the node and left-specific expression of Nodal in the lateral plate mesoderm, a hallmark gene in LR patterning, Notch signaling also suppresses the expression of Pitx2 that is a direct downstream target of Nodal during later stages of development. This negative activity of Notch signaling towards left-specific activity was recently shown to be inhibited by the B cell lymphoma 6 (BCL6)/BCL6 co-repressor (BcoR) transcriptional repressor complex in a target-specific manner. The complex regulation of Notch-dependent gene expression for LR asymmetry will be highlighted in this review.
左右(LR)不对称的建立受胚胎发生过程中复杂的信号机制调节,这种不对称对于形态发生以及生物体内部器官的定位至关重要。最近的进展包括离子转运体、向左的节点流以及不对称基因表达的调节,有助于我们理解对称性是如何被打破的,以及这种左右信息是如何随后传递到器官原基的。许多发育信号通路都参与了这一复杂过程。在这篇综述中,我们将重点介绍 Notch 信号通路在 LR 不对称发育中的作用。Notch 信号通路是相邻细胞之间的短程通讯系统。虽然 Notch 信号在调节节点的形态发生和侧板中胚层中 Nodal 的左特异性表达(LR 模式化的标志性基因)中发挥重要作用,但 Notch 信号也抑制了 Pitx2 的表达,而 Pitx2 是 Nodal 的直接下游靶基因在发育的后期阶段。最近的研究表明,Notch 信号对左特异性活性的这种负性活性被 B 细胞淋巴瘤 6(BCL6)/BCL6 共抑制因子(BcoR)转录抑制复合物以特定于靶标的方式抑制。本文将重点介绍 Notch 依赖性基因表达对 LR 不对称性的复杂调节。