Kotera Ippei, Sekimoto Toshihiro, Miyamoto Yoichi, Saiwaki Takuya, Nagoshi Emi, Sakagami Hiroyuki, Kondo Hisatake, Yoneda Yoshihiro
Department of Cell Biology and Neuroscience, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
EMBO J. 2005 Mar 9;24(5):942-51. doi: 10.1038/sj.emboj.7600587. Epub 2005 Feb 17.
Ca(2+)/calmodulin-dependent protein kinase type IV (CaMKIV) plays an essential role in the transcriptional activation of cAMP response element-binding protein-mediated signaling pathways. Although CaMKIV is localized predominantly in the nucleus, the molecular mechanism of the nuclear import of CaMKIV has not been elucidated. We report here that importin alpha is able to carry CaMKIV into the nucleus without the need for importin beta or any other soluble proteins in digitonin-permeabilized cells. An importin beta binding-deficient mutant (DeltaIBB) of importin alpha also carried CaMKIV into the nucleus, which strongly suggests that CaMKIV is transported in an importin beta-independent manner. While CaMKIV directly interacted with the C-terminal region of importin alpha, the CaMKIV/importin alpha complex did not form a ternary complex with importin beta, which explains the nonrequirement of importin beta for the nuclear transport of CaMKIV. The cytoplasmic microinjection of importin alpha-DeltaIBB enhanced the rate of nuclear translocation of CaMKIV in vivo. This is the first report to demonstrate definitely that mammalian importin alpha solely carries a cargo protein into the nucleus without utilizing the classical importin beta-dependent transport system.
钙/钙调蛋白依赖性蛋白激酶IV(CaMKIV)在环磷酸腺苷反应元件结合蛋白介导的信号通路的转录激活中起重要作用。尽管CaMKIV主要定位于细胞核,但CaMKIV核输入的分子机制尚未阐明。我们在此报告,在洋地黄皂苷通透的细胞中,输入蛋白α能够将CaMKIV带入细胞核,而无需输入蛋白β或任何其他可溶性蛋白。输入蛋白α的一个缺乏输入蛋白β结合能力的突变体(DeltaIBB)也能将CaMKIV带入细胞核,这强烈表明CaMKIV是以不依赖输入蛋白β的方式运输的。虽然CaMKIV直接与输入蛋白α的C末端区域相互作用,但CaMKIV/输入蛋白α复合物并未与输入蛋白β形成三元复合物。这就解释了CaMKIV核运输不需要输入蛋白β的原因。在体内对输入蛋白α-DeltaIBB进行细胞质显微注射提高了CaMKIV核转位的速率。这是第一份明确证明哺乳动物输入蛋白α在不利用经典的依赖输入蛋白β的运输系统的情况下,仅将一种货物蛋白带入细胞核的报告。