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由JNK信号转导通路对抗的NFAT4核内积聚。

Nuclear accumulation of NFAT4 opposed by the JNK signal transduction pathway.

作者信息

Chow C W, Rincón M, Cavanagh J, Dickens M, Davis R J

机构信息

Howard Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Science. 1997 Nov 28;278(5343):1638-41. doi: 10.1126/science.278.5343.1638.

Abstract

The nuclear factor of activated T cells (NFAT) group of transcription factors is retained in the cytoplasm of quiescent cells. NFAT activation is mediated in part by induced nuclear import. This process requires calcium-dependent dephosphorylation of NFAT caused by the phosphatase calcineurin. The c-Jun amino-terminal kinase (JNK) phosphorylates NFAT4 on two sites. Mutational removal of the JNK phosphorylation sites caused constitutive nuclear localization of NFAT4. In contrast, JNK activation in calcineurin-stimulated cells caused nuclear exclusion of NFAT4. These findings show that the nuclear accumulation of NFAT4 promoted by calcineurin is opposed by the JNK signal transduction pathway.

摘要

活化T细胞核因子(NFAT)转录因子组在静止细胞的细胞质中保持存在。NFAT的激活部分是由诱导的核输入介导的。这个过程需要磷酸酶钙调神经磷酸酶引起的NFAT的钙依赖性去磷酸化。c-Jun氨基末端激酶(JNK)在两个位点使NFAT4磷酸化。JNK磷酸化位点的突变去除导致NFAT4的组成型核定位。相反,在钙调神经磷酸酶刺激的细胞中JNK激活导致NFAT4的核排除。这些发现表明,钙调神经磷酸酶促进的NFAT4的核积累受到JNK信号转导途径的对抗。

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