Ridley Anne J
Randall Division of Cell and Molecular Biophysics, King's College London, London, UK.
Methods Mol Biol. 2012;827:3-12. doi: 10.1007/978-1-61779-442-1_1.
In 1985, the first members of the Rho GTPase family were identified. Over the next 10 years, rapid progress was made in understanding Rho GTPase signalling. Multiple Rho GTPases were discovered in a wide range of eukaryotes, and shown to regulate a diverse range of cellular processes, including cytoskeletal dynamics, NADPH oxidase activation, cell migration, cell polarity, membrane trafficking, and transcription. The Rho regulators, guanine nucleotide exchange factors (GEFs), GTPase-activating proteins (GAPs), and guanine nucleotide dissociation inhibitors (GDIs), were found through a combination of biochemistry, genetics, and detective work. Downstream targets for Rho GTPases were also rapidly identified, and linked to Rho-regulated cellular responses. In parallel, a wide range of bacterial proteins were found to modify Rho proteins or alter their activity in cells, many of which turned out to be useful tools to study Rho functions. More recent work has delineated where Rho GTPases act in cells, the molecular pathways linking some of them to specific cellular responses, and their functions in the development of multicellular organisms.
1985年,Rho GTP酶家族的首批成员被鉴定出来。在接下来的10年里,对Rho GTP酶信号传导的理解取得了迅速进展。多种Rho GTP酶在广泛的真核生物中被发现,并被证明可调节多种细胞过程,包括细胞骨架动力学、NADPH氧化酶激活、细胞迁移、细胞极性、膜运输和转录。通过生物化学、遗传学和探索性研究相结合的方式,发现了Rho调节因子,即鸟嘌呤核苷酸交换因子(GEFs)、GTP酶激活蛋白(GAPs)和鸟嘌呤核苷酸解离抑制剂(GDIs)。Rho GTP酶的下游靶点也很快被确定,并与Rho调节的细胞反应相关联。与此同时,人们发现了多种细菌蛋白可修饰Rho蛋白或改变其在细胞中的活性,其中许多后来成为研究Rho功能的有用工具。最近的研究已经阐明了Rho GTP酶在细胞中的作用位置、将其中一些与特定细胞反应联系起来的分子途径,以及它们在多细胞生物发育中的功能。