Gloeckner Christian Johannes, Schumacher Annette, Boldt Karsten, Ueffing Marius
Department of Protein Science, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
J Neurochem. 2009 May;109(4):959-68. doi: 10.1111/j.1471-4159.2009.06024.x. Epub 2009 Mar 3.
Autosomal dominant mutations in the human Leucine-Rich Repeat Kinase 2 (LRRK2) gene represent the most common monogenetic cause of Parkinson disease (PD) and increased kinase activity observed in pathogenic mutants of LRRK2 is most likely causative for PD-associated neurotoxicity. The sequence of the LRRK2 kinase domain shows similarity to MAP kinase kinase kinases. Furthermore, LRRK2 shares highest sequence homology with mixed linage kinases which act upstream of canonical MAPKK and are involved in cellular stress responses. Therefore, we addressed the question if LRRK2 exhibits MAPKKK activity by systematically testing MAPKKs as candidate substrates, in vitro. We demonstrate that LRRK2 variants phosphorylate mitogen-activated protein kinase kinases (MAPKK), including MKK3 -4, -6 and -7. MKKs act upstream of the MAPK p38 and JNK mediating oxidative cell stress, neurotoxicity and apoptosis. The disease-associated LRRK2 G2019S and I2020T mutations show an increased phosphotransferase activity towards MKKs correlating with the activity shown for its autophosphorylation. Our findings present evidence of a new class of molecular targets for mutant LRRK2 that link to neurotoxicity, cellular stress, cytoskeletal dynamics and vesicular transport.
人类富亮氨酸重复激酶2(LRRK2)基因中的常染色体显性突变是帕金森病(PD)最常见的单基因病因,在LRRK2致病突变体中观察到的激酶活性增加很可能是PD相关神经毒性的病因。LRRK2激酶结构域的序列与丝裂原活化蛋白激酶激酶激酶相似。此外,LRRK2与混合谱系激酶具有最高的序列同源性,混合谱系激酶在经典MAPKK上游起作用并参与细胞应激反应。因此,我们通过在体外系统地测试MAPKK作为候选底物,探讨了LRRK2是否具有MAPKKK活性的问题。我们证明LRRK2变体可磷酸化丝裂原活化蛋白激酶激酶(MAPKK),包括MKK3 -4、-6和-7。MKK在MAPK p38和JNK上游起作用,介导氧化细胞应激、神经毒性和细胞凋亡。与疾病相关的LRRK2 G2019S和I2020T突变显示对MKK的磷酸转移酶活性增加,这与其自身磷酸化所显示的活性相关。我们的研究结果为突变型LRRK2的一类新分子靶点提供了证据,这些靶点与神经毒性、细胞应激、细胞骨架动力学和囊泡运输有关。