Xia C, Ma W, Stafford L J, Marcus S, Xiong W C, Liu M
Center for Cancer Biology and Nutrition, Institute of Biosciences and Technology, and Department of Medical Biochemistry and Genetics, Texas A&M University System Health Science Center, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 2001 May 22;98(11):6174-9. doi: 10.1073/pnas.101137298.
The family of p21-activated protein kinases (PAKs) is composed of serine-threonine kinases whose activity is regulated by the small guanosine triphosphatases (GTPases) Rac and Cdc42. In mammalian cells, PAKs have been implicated in the regulation of mitogen-activated protein cascades, cellular morphological and cytoskeletal changes, neurite outgrowth, and cell apoptosis. Although the ability of Cdc42 and Rac GTPases to activate PAK is well established, relatively little is known about the negative regulation of PAK or the identity of PAK cellular targets. Here, we describe the identification and characterization of a human PAK-interacting protein, hPIP1. hPIP1 contains G protein beta-like WD repeats and shares sequence homology with the essential fission yeast PAK regulator, Skb15, as well as the essential budding yeast protein, MAK11. Interaction of hPIP1 with PAK1 inhibits the Cdc42/Rac-stimulated kinase activity through the N-terminal regulatory domains of PAK1. Cotransfection of hPIP1 in mammalian cells inhibits PAK-mediated c-Jun N-terminal kinase and nuclear factor kappa B signaling pathways. Our results demonstrate that hPIP1 is a negative regulator of PAK and PAK signaling pathways.
p21激活蛋白激酶(PAK)家族由丝氨酸 - 苏氨酸激酶组成,其活性受小GTP酶(GTPases)Rac和Cdc42调节。在哺乳动物细胞中,PAK参与有丝分裂原激活蛋白级联反应的调节、细胞形态和细胞骨架变化、神经突生长以及细胞凋亡。虽然Cdc42和Rac GTPases激活PAK的能力已得到充分证实,但关于PAK的负调节或PAK细胞靶点的身份了解相对较少。在这里,我们描述了一种人类PAK相互作用蛋白hPIP1的鉴定和表征。hPIP1包含G蛋白β样WD重复序列,并与重要的裂殖酵母PAK调节因子Skb15以及重要的芽殖酵母蛋白MAK11具有序列同源性。hPIP1与PAK1的相互作用通过PAK1的N端调节域抑制Cdc42/Rac刺激的激酶活性。在哺乳动物细胞中共转染hPIP1可抑制PAK介导的c-Jun N端激酶和核因子κB信号通路。我们的结果表明,hPIP1是PAK和PAK信号通路的负调节因子。