Unit of Neuromuscular Disorders, Translational Pediatrics and Clinical Genetics, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Molecular Genetics and Functional Genomics, Bambino Gesù Children's Research Hospital, IRCCS, 00146 Rome, Italy.
Int J Mol Sci. 2023 Feb 1;24(3):2781. doi: 10.3390/ijms24032781.
Microtubules (MTs) are dynamic components of the cell cytoskeleton involved in several cellular functions, such as structural support, migration and intracellular trafficking. Despite their high similarity, MTs have functional heterogeneity that is generated by the incorporation into the MT lattice of different tubulin gene products and by their post-translational modifications (PTMs). Such regulations, besides modulating the tubulin composition of MTs, create on their surface a "biochemical code" that is translated, through the action of protein effectors, into specific MT-based functions. This code, known as "tubulin code", plays an important role in neuronal cells, whose highly specialized morphologies and activities depend on the correct functioning of the MT cytoskeleton and on its interplay with a myriad of MT-interacting proteins. In recent years, a growing number of mutations in genes encoding for tubulins, MT-interacting proteins and enzymes that post-translationally modify MTs, which are the main players of the tubulin code, have been linked to neurodegenerative processes or abnormalities in neural migration, differentiation and connectivity. Nevertheless, the exact molecular mechanisms through which the cell writes and, downstream, MT-interacting proteins decipher the tubulin code are still largely uncharted. The purpose of this review is to describe the molecular determinants and the readout mechanisms of the tubulin code, and briefly elucidate how they coordinate MT behavior during critical neuronal events, such as neuron migration, maturation and axonal transport.
微管(MTs)是细胞骨架的动态组成部分,参与多种细胞功能,如结构支持、迁移和细胞内运输。尽管它们高度相似,但 MTs 具有功能异质性,这是通过将不同的微管蛋白基因产物掺入 MT 晶格中和通过它们的翻译后修饰(PTMs)产生的。这种调节除了调节 MT 的微管蛋白组成外,还在其表面创建了一个“生化密码”,通过蛋白质效应物的作用,将其转化为特定的基于 MT 的功能。这个密码,称为“微管蛋白密码”,在神经元细胞中起着重要作用,其高度特化的形态和活动依赖于 MT 细胞骨架的正确功能及其与无数 MT 相互作用蛋白的相互作用。近年来,越来越多的编码微管蛋白、MT 相互作用蛋白和翻译后修饰 MT 的酶的基因突变与神经退行性过程或神经迁移、分化和连接异常有关。然而,细胞编写微管蛋白密码的精确分子机制以及 MT 相互作用蛋白的下游解码机制仍在很大程度上未知。本综述的目的是描述微管蛋白密码的分子决定因素和读出机制,并简要阐明它们如何协调 MT 在关键神经元事件中的行为,如神经元迁移、成熟和轴突运输。