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Endophilin regulates JNK activation through its interaction with the germinal center kinase-like kinase

机译:内啡肽通过与生发中心激酶样激酶相互作用来调节JNK活化

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摘要

The endophilin family of proteins function in clathrin-mediated endocytosis. Here, we have identified and cloned the rat germinal center kinase-like kinase (rGLK), a member of the GCK (germinal center kinase) family of e-Jun N-terminal kinase (JNK) activating enzymes, as a novel endophilin I-binding partner. The interaction occurs both in vitro and in cells and is mediated by the Src homology 3 domain of endophilin I and a region of rGLK containing the endophilin consensus-binding sequence PPRPPPPR. Overlay analysis of rat brain extracts demonstrates that endophilin I is a major Src homology 3 domain-binding partner for rGLK. Overexpression of full-length endophilin I activates rGLK-mediated JNK activation, whereas N- and C-terminal fragments of endophilin I block JNK activation. Thus, endophilin I appears to have a novel function in JNK activation.
机译:内啡肽家族蛋白在网格蛋白介导的内吞作用中起作用。在这里,我们已经鉴定并克隆了大鼠生发中心激酶样激酶(rGLK),它是e-Jun N端激酶(JNK)激活酶的GCK(生殖中心激酶)家族的成员,是一种新型的内啡肽有约束力的伙伴。相互作用在体外和细胞中均发生,并由内啡肽I的Src同源3结构域和包含内啡肽共有结合序列PPRPPPPR的rGLK区域介导。对大鼠脑提取物的叠加分析表明,内皮糖蛋白I是rGLK的主要Src同源性3结构域结合伴侣。全长内啡肽I的过表达会激活rGLK介导的JNK激活,而内啡肽I的N和C端片段会阻止JNK激活。因此,内啡肽I在JNK激活中似乎具有新功能。

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