School of Physics, University of New South Wales, Sydney 2052, Australia.
Department of Molecular Sciences, Macquarie University, Sydney 2109, Australia.
Int J Mol Sci. 2019 Apr 23;20(8):1996. doi: 10.3390/ijms20081996.
The merlin-ERM (ezrin, radixin, moesin) family of proteins plays a central role in linking the cellular membranes to the cortical actin cytoskeleton. Merlin regulates contact inhibition and is an integral part of cell-cell junctions, while ERM proteins, ezrin, radixin and moesin, assist in the formation and maintenance of specialized plasma membrane structures and membrane vesicle structures. These two protein families share a common evolutionary history, having arisen and separated via gene duplication near the origin of metazoa. During approximately 0.5 billion years of evolution, the merlin and ERM family proteins have maintained both sequence and structural conservation to an extraordinary level. Comparing crystal structures of merlin-ERM proteins and their complexes, a picture emerges of the merlin-ERM proteins acting as switchable interaction hubs, assembling protein complexes on cellular membranes and linking them to the actin cytoskeleton. Given the high level of structural conservation between the merlin and ERM family proteins we speculate that they may function together.
Merlin-ERM(埃兹蛋白、根蛋白和膜突蛋白)家族蛋白在将细胞膜与皮质肌动蛋白细胞骨架连接中起着核心作用。Merlin 调节接触抑制,是细胞-细胞连接的一个组成部分,而 ERM 蛋白(埃兹蛋白、根蛋白和膜突蛋白)则有助于形成和维持特殊的质膜结构和膜囊泡结构。这两个蛋白家族具有共同的进化历史,它们通过在后生动物起源附近的基因复制而出现和分离。在大约 5 亿年的进化过程中,Merlin 和 ERM 家族蛋白保持了序列和结构的高度保守性。通过比较 Merlin-ERM 蛋白及其复合物的晶体结构,形成了 Merlin-ERM 蛋白作为可切换相互作用枢纽的图像,它们在细胞膜上组装蛋白复合物并将其与肌动蛋白细胞骨架连接。鉴于 Merlin 和 ERM 家族蛋白之间的结构高度保守,我们推测它们可能一起发挥作用。