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酪蛋白激酶I和丝裂原活化蛋白激酶激酶激酶1对活化T细胞核因子4上核输入信号的分子内掩蔽作用。

Intramolecular masking of nuclear import signal on NF-AT4 by casein kinase I and MEKK1.

作者信息

Zhu J, Shibasaki F, Price R, Guillemot J C, Yano T, Dötsch V, Wagner G, Ferrara P, McKeon F

机构信息

Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Cell. 1998 May 29;93(5):851-61. doi: 10.1016/s0092-8674(00)81445-2.

Abstract

T cell activation requires the import of NF-AT transcription factors to the nucleus, a process promoted by calcineurin-dependent dephosphorylation and inhibited by poorly understood protein kinases. Here, we report the identification of two protein kinases that oppose NF-AT4 nuclear import. Casein kinase Ialpha directly binds and phosphorylates NF-AT4, resulting in the inhibiton of NF-AT4 nuclear translocation. MEKK1 indirectly suppresses NF-AT4 nuclear import by stabilizing the interaction between NF-AT4 and CKIalpha. CKIalpha thus acts to establish an intramolecular masking of the nuclear location signal on NF-AT4, while MEKK1 augments this mechanism, and may further provide a link to signal transduction pathways regulating NF-AT4.

摘要

T细胞活化需要将NF-AT转录因子导入细胞核,这一过程由钙调神经磷酸酶依赖性去磷酸化促进,并受到了解甚少的蛋白激酶的抑制。在此,我们报告鉴定出两种对抗NF-AT4核输入的蛋白激酶。酪蛋白激酶Iα直接结合并磷酸化NF-AT4,导致NF-AT4核转运受到抑制。MEKK1通过稳定NF-AT4与CKIα之间的相互作用间接抑制NF-AT4核输入。因此,CKIα起到对NF-AT4上的核定位信号进行分子内掩盖的作用,而MEKK1增强了这一机制,并且可能进一步提供与调节NF-AT4的信号转导途径的联系。

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