Lang Charles F, Munro Edwin
Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL 60637, USA.
Committee on Genetics, Genomics and Systems Biology, University of Chicago, Chicago, IL 60637, USA.
Development. 2017 Oct 1;144(19):3405-3416. doi: 10.1242/dev.139063.
PAR proteins constitute a highly conserved network of scaffolding proteins, adaptors and enzymes that form and stabilize cortical asymmetries in response to diverse inputs. They function throughout development and across the metazoa to regulate cell polarity. In recent years, traditional approaches to identifying and characterizing molecular players and interactions in the PAR network have begun to merge with biophysical, theoretical and computational efforts to understand the network as a pattern-forming biochemical circuit. Here, we summarize recent progress in the field, focusing on recent studies that have characterized the core molecular circuitry, circuit design and spatiotemporal dynamics. We also consider some of the ways in which the PAR network has evolved to polarize cells in different contexts and in response to different cues and functional constraints.
PAR蛋白构成了一个由支架蛋白、衔接蛋白和酶组成的高度保守的网络,这些蛋白会根据不同的输入形成并稳定皮层不对称性。它们在整个发育过程以及后生动物中发挥作用,以调节细胞极性。近年来,识别和表征PAR网络中分子参与者及相互作用的传统方法,已开始与生物物理、理论和计算方面的努力相结合,以便将该网络理解为一个形成模式的生化回路。在这里,我们总结了该领域的最新进展,重点关注了那些对核心分子电路、电路设计以及时空动态进行了表征的近期研究。我们还思考了PAR网络在不同背景下以及对不同信号和功能限制做出反应时,是如何进化以实现细胞极化的一些方式。