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Interlocked positive and negative feedback network motifs regulate beta-catenin activity in the adherens junction pathway

机译:正负反馈网络互锁,调节粘附连接途径中的β-catenin活性

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摘要

The integrity of epithelial tissue architecture is maintained through adherens junctions that are created through extracellular homotypic protein-protein interactions between cadherin molecules. Cadherins also provide an intracellular scaffold for the formation of a multiprotein complex that contains signaling proteins, including beta-catenin. Environmental factors and controlled tissue reorganization disrupt adherens junctions by cleaving the extracellular binding domain and initiating a series of transcriptional events that aim to restore tissue homeostasis. However, it remains unclear how alterations in cell adhesion coordinate transcriptional events, including those mediated by beta-catenin in this pathway. Here were used quantitative single-cell and population-level in vitro assays to quantify the endogenous pathway dynamics after the proteolytic disruption of the adherens junctions. Using prior knowledge of isolated elements of the overall network, we interpreted these data using in silico model-based inference to identify the topology of the regulatory network. Collectively the data suggest that the regulatory network contains interlocked network motifs consisting of a positive feedback loop, which is used to restore the integrity of adherens junctions, and a negative feedback loop, which is used to limit beta-catenin-induced gene expression.
机译:上皮组织结构的完整性通过钙粘着蛋白分子之间的细胞外同型蛋白-蛋白相互作用产生的粘附连接来维持。钙黏着蛋白还为形成包含信号蛋白(包括β-连环蛋白)的多蛋白复合物提供了细胞内支架。环境因素和受控的组织重组通过切割细胞外结合结构域并启动一系列旨在恢复组织稳态的转录事件,破坏了粘附连接。但是,尚不清楚细胞粘附的改变如何协调转录事件,包括在该途径中由β-连环蛋白介导的转录事件。在这里使用定量单细胞和群体水平的体外测定法来量化粘附连接的蛋白水解破坏后的内源性途径动力学。利用整个网络隔离元素的先验知识,我们使用基于计算机模型的推理来解释这些数据,以识别监管网络的拓扑。总体而言,数据表明调节网络包含互锁的网络图案,其中包括一个正反馈环(用于恢复粘附连接的完整性)和一个负反馈环(用于限制β-连环蛋白诱导的基因表达)。

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