Zhao Zhuo-Shen, Manser Ed
sGSK Group; Astar Neuroscience Research Partnership; Singapore.
Cell Logist. 2012 Apr 1;2(2):59-68. doi: 10.4161/cl.21912.
The p21-activated kinases (PAKs) are a family of Ser/Thr protein kinases that are represented by six genes in humans (PAK 1-6), and are found in all eukaryotes sequenced to date. Genetic and knockdown experiments in frogs, fish and mice indicate group I PAKs are widely expressed, required for multiple tissue development, and particularly important for immune and nervous system function in the adult. The group II PAKs (human PAKs 4-6) are more enigmatic, but their restriction to metazoans and presence at cell-cell junctions suggests these kinases emerged to regulate junctional signaling. Studies of protozoa and fungal PAKs show that they regulate cell shape and polarity through phosphorylation of multiple cytoskeletal proteins, including microtubule binding proteins, myosins and septins. This chapter discusses what we know about the regulation of PAKs and their physiological role in different model organisms, based primarily on gene knockout studies.
p21激活激酶(PAKs)是一类丝氨酸/苏氨酸蛋白激酶,在人类中由六个基因(PAK 1 - 6)代表,并且在迄今测序的所有真核生物中都有发现。在青蛙、鱼类和小鼠中进行的基因和基因敲除实验表明,I组PAKs广泛表达,是多种组织发育所必需的,并且对成年动物的免疫和神经系统功能尤为重要。II组PAKs(人类PAKs 4 - 6)则更为神秘,但它们仅限于后生动物且存在于细胞间连接处,这表明这些激酶的出现是为了调节连接信号。对原生动物和真菌PAKs的研究表明,它们通过磷酸化多种细胞骨架蛋白(包括微管结合蛋白、肌球蛋白和隔膜蛋白)来调节细胞形状和极性。本章主要基于基因敲除研究,讨论我们对PAKs调控及其在不同模式生物中的生理作用的了解。