| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 2051751 | FEBS Letters | 2007 | 7 Pages | 
Abstract
												Different scaffold proteins play distinct roles in various signaling pathways by recruiting different downstream molecules. Here, using MKK4−/− and MKK4−/−/7−/− murine embryonic fibroblast cells, we examined differential employment of MKK4 and MKK7 by scaffold proteins Axin, Dvl, and Epstein–Barr virus latent membrane protein-1 (LMP-1) in mediating JNK activation. We present evidence that Axin depends mainly on MKK7 for activation of JNK, while Dvl depends almost equally on MKK4 and MKK7 for JNK activation, In contrast, LMP-1-induced JNK activation is primarily dependent on MKK4. Our results demonstrate that Axin, Dvl, and LMP-1 differentially utilize MKK4 and MKK7 for JNK activation.
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											Authors
												Haiying Zou, Qinxi Li, Sheng-Cai Lin, Zhenguo Wu, Jiahuai Han, Zhiyun Ye, 
											