Couillard-Despres Sebastien, Uyanik Goekhan, Ploetz Sonja, Karl Claudia, Koch Hartmut, Winkler Juergen, Aigner Ludwig
Department of Neurology, University of Regensburg, Franz Josef Strauss Allee 11, 93053 Regensburg, Germany.
Neurogenetics. 2004 Jun;5(2):83-93. doi: 10.1007/s10048-004-0176-1. Epub 2004 Mar 25.
Mutations in doublecortin ( DCX) affect the migration of neuronal precursor cells and cause subcortical band heterotopia and lissencephaly. DCX is known to bind and bundle microtubules; however, the impact of mutation on DCX function and its relation to the manifestation of DCX-associated disorders is still unclear. We analyzed the impact of DCX mutants on COS7 cell microtubule networks. We found that both mutant and wild type DCX are able to bind and bundle microtubules; however, mutants possess a decreased ability to perturb the mitotic machinery, to cause abnormal spindle orientation, and to impair mitotic progression. The magnitude of this decrease is proportional to the severity of the mutation-associated clinical symptoms, thereby providing a cell-based assay for the prognosis of DCX-associated neuronal migration disorders.
双皮质素(DCX)突变会影响神经元前体细胞的迁移,并导致皮质下带状异位和无脑回畸形。已知DCX能结合并捆绑微管;然而,突变对DCX功能的影响及其与DCX相关疾病表现的关系仍不清楚。我们分析了DCX突变体对COS7细胞微管网络的影响。我们发现,突变型和野生型DCX都能够结合并捆绑微管;然而,突变体干扰有丝分裂机制、导致异常纺锤体定向以及损害有丝分裂进程的能力下降。这种下降的程度与突变相关临床症状的严重程度成正比,从而为DCX相关神经元迁移障碍的预后提供了一种基于细胞的检测方法。