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
College of Pharmacy and Research Institute of Drug Development, Chonnam National University, Gwangju 500-757, Korea.
J Biol Chem. 2008 Jan 11;283(2):977-87. doi: 10.1074/jbc.M707158200. Epub 2007 Nov 8.
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.
δ-连环蛋白最初是通过其与早老素-1的相互作用而被鉴定出来的,并且与树突发生和认知功能的调节有关。然而,δ-连环蛋白促进树突形态发生的分子机制尚不清楚。在本研究中,我们证明了δ-连环蛋白与p190RhoGEF的相互作用,以及Akt1介导的δ-连环蛋白苏氨酸-454残基磷酸化在这种相互作用中的重要性。我们还发现,δ-连环蛋白的过表达降低了p190RhoGEF与RhoA之间的结合,并显著降低了GTP-RhoA的水平,但不影响GTP-Rac1和-Cdc42的水平。δ-连环蛋白T454A是一种在p190RhoGEF结合方面有缺陷的形式,它并没有降低p190RhoGEF与RhoA之间的结合。δ-连环蛋白T454A也没有降低GTP-RhoA的水平,并且未能在NIH 3T3成纤维细胞中诱导树突样突起的形成。此外,δ-连环蛋白T454A显著减少了原代海马神经元中成熟蘑菇状棘突的长度和数量。这些结果突出了δ-连环蛋白诱导的树突发生和棘突形态发生调节中的信号事件。