Zhao Z S, Manser E, Chen X Q, Chong C, Leung T, Lim L
Glaxo-IMCB Group, Institute of Molecular & Cell Biology, Singapore, Singapore.
Mol Cell Biol. 1998 Apr;18(4):2153-63. doi: 10.1128/MCB.18.4.2153.
AlphaPAK in a constitutively active form can exert morphological effects (E. Manser, H.-Y. Huang, T.-H. Loo, X.-Q. Chen, J.-M. Dong, T. Leung, and L. Lim, Mol. Cell. Biol. 17:1129-1143, 1997) resembling those of Cdc42G12V. PAK family kinases, conserved from yeasts to humans, are directly activated by Cdc42 or Rac1 through interaction with a conserved N-terminal motif (corresponding to residues 71 to 137 in alphaPAK). alphaPAK mutants with substitutions in this motif that resulted in severely reduced Cdc42 binding can be recruited normally to Cdc42G12V-driven focal complexes. Mutation of residues in the C-terminal portion of the motif (residues 101 to 137), though not affecting Cdc42 binding, produced a constitutively active kinase, suggesting this to be a negative regulatory region. Indeed, a 67-residue polypeptide encoding alphaPAK83-149 potently inhibited GTPgammaS-bound Cdc42-mediated kinase activation of both alphaPAK and betaPAK. Coexpression of this PAK inhibitor with Cdc42G12V prevented the formation of peripheral actin microspikes and associated loss of stress fibers normally induced by the p21. Coexpression of PAK inhibitor with Rac1G12V also prevented loss of stress fibers but not ruffling induced by the p21. Coexpression of alphaPAK83-149 completely blocked the phenotypic effects of hyperactive alphaPAKL107F in promoting dissolution of focal adhesions and actin stress fibers. These results, coupled with previous observations with constitutively active PAK, demonstrate that these kinases play an important role downstream of Cdc42 and Rac1 in cytoskeletal reorganization.
组成型活性形式的αPAK可发挥类似于Cdc42G12V的形态学效应(E. Manser、H.-Y. Huang、T.-H. Loo、X.-Q. Chen、J.-M. Dong、T. Leung和L. Lim,《分子与细胞生物学》17:1129 - 1143,1997年)。从酵母到人类保守的PAK家族激酶通过与保守的N端基序(对应于αPAK中的71至137位残基)相互作用而被Cdc42或Rac1直接激活。该基序中发生取代导致Cdc42结合严重减少的αPAK突变体能够正常募集到由Cdc42G12V驱动的粘着斑复合体。该基序C端部分(101至137位残基)的残基突变虽然不影响Cdc42结合,但产生了组成型活性激酶,表明这是一个负调控区域。实际上,编码αPAK83 - 149的67个残基的多肽强烈抑制了GTPγS结合的Cdc42介导的αPAK和βPAK的激酶激活。该PAK抑制剂与Cdc42G12V共表达可防止外周肌动蛋白微刺的形成以及通常由p21诱导的应力纤维的相关丧失。PAK抑制剂与Rac1G12V共表达也可防止应力纤维的丧失,但不能防止由p21诱导的边缘波动。αPAK83 - 149共表达完全阻断了活性过高的αPAKL107F在促进粘着斑和肌动蛋白应力纤维溶解方面的表型效应。这些结果,再加上之前对组成型活性PAK的观察,表明这些激酶在细胞骨架重组中Cdc42和Rac1的下游发挥重要作用。