Delta-catenin was first identified through its interaction with Presenilin-1 and has been implicated in the regulation of dendrogenesis and cognitive function. However, the molecular mechanisms by which delta-catenin promotes dendritic morphogenesis were unclear. In this study, we demonstrated delta-catenin interaction with p190RhoGEF, and the importance of Akt1-mediated phosphorylation at Thr-454 residue of delta-catenin in this interaction. We have also found that delta-catenin overexpression decreased the binding between p190RhoGEF and RhoA, and significantly lowered the levels of GTP-RhoA but not those of GTP-Rac1 and -Cdc42. Delta-catenin T454A, a defective form in p190RhoGEF binding, did not decrease the binding between p190RhoGEF and RhoA. Delta-catenin T454A also did not lower GTP-RhoA levels and failed to induce dendrite-like process formation in NIH 3T3 fibroblasts. Furthermore, delta-catenin T454A significantly reduced the length and number of mature mushroom shaped spines in primary hippocampal neurons. These results highlight signaling events in the regulation of delta-catenin-induced dendrogenesis and spine morphogenesis.
Delta-catenin-induced dendritic morphogenesis. An essential role of p190RhoGEF interaction through Akt1-mediated phosphorylation.
Delta-catenin诱导的树突形态发生p190RhoGEF通过Akt1介导的磷酸化作用发挥关键作用
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作者:Kim Hangun, Han Jeong-Ran, Park Jaejun, Oh Minsoo, James Sarah E, Chang Sunghoe, Lu Qun, Lee Kwang Youl, Ki Hyunkyoung, Song Woo-Joo, Kim Kwonseop
| 期刊: | Journal of Biological Chemistry | 影响因子: | 3.900 |
| 时间: | 2008 | 起止号: | 2008 Jan 11; 283(2):977-87 |
| doi: | 10.1074/jbc.M707158200 | 靶点: | AKT1 |
| 研究方向: | 表观遗传 | ||
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