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糖原合酶激酶-3增强NF-ATc的核输出。

Nuclear export of NF-ATc enhanced by glycogen synthase kinase-3.

作者信息

Beals C R, Sheridan C M, Turck C W, Gardner P, Crabtree G R

机构信息

Howard Hughes Medical Institute, Department of Developmental Biology, Stanford University, Stanford, CA 94305, USA.

出版信息

Science. 1997 Mar 28;275(5308):1930-4. doi: 10.1126/science.275.5308.1930.

Abstract

The transcription factor NF-AT responds to Ca2+-calcineurin signals by translocating to the nucleus, where it participates in the activation of early immune response genes. Calcineurin dephosphorylates conserved serine residues in the amino terminus of NF-AT, resulting in nuclear import. Purification of the NF-AT kinase revealed that it is composed of a priming kinase activity and glycogen synthase kinase-3 (GSK-3). GSK-3 phosphorylates conserved serines necessary for nuclear export, promotes nuclear exit, and thereby opposes Ca2+-calcineurin signaling. Because GSK-3 responds to signals initiated by Wnt and other ligands, NF-AT family members could be effectors of these pathways.

摘要

转录因子NF-AT通过易位至细胞核来响应Ca2+ -钙调神经磷酸酶信号,在细胞核中它参与早期免疫反应基因的激活。钙调神经磷酸酶使NF-AT氨基末端保守的丝氨酸残基去磷酸化,从而导致核输入。对NF-AT激酶的纯化显示它由一种引发激酶活性和糖原合酶激酶-3(GSK-3)组成。GSK-3使核输出所需的保守丝氨酸磷酸化,促进核输出,从而对抗Ca2+ -钙调神经磷酸酶信号。由于GSK-3对由Wnt和其他配体引发的信号作出反应,NF-AT家族成员可能是这些信号通路的效应器。

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