De Angelis E, MacFarlane J, Du J S, Yeo G, Hicks R, Rathjen F G, Kenwrick S, Brümmendorf T
Cambridge Institute for Medical Research, University of Cambridge Clinical School, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2XY, UK.
EMBO J. 1999 Sep 1;18(17):4744-53. doi: 10.1093/emboj/18.17.4744.
Mutations in the gene for neural cell adhesion molecule L1 (L1CAM) result in a debilitating X-linked congenital disorder of brain development. At the neuronal cell surface L1 may interact with a variety of different molecules including itself and two other CAMs of the immunoglobulin superfamily, axonin-1 and F11. However, whether all of these interactions are relevant to normal or abnormal development has not been determined. Over one-third of patient mutations are single amino acid changes distributed across 10 extracellular L1 domains. We have studied the effects of 12 missense mutations on binding to L1, axonin-1 and F11 and shown for the first time that whereas many mutations affect all three interactions, others affect homophilic or heterophilic binding alone. Patient pathology is therefore due to different types of L1 malfunction. The nature and functional consequence of mutation is also reflected in the severity of the resultant phenotype with structural mutations likely to affect more than one binding activity and result in early mortality. Moreover, the data indicate that several extracellular domains of L1 are required for homophilic and heterophilic interactions.
神经细胞黏附分子L1(L1CAM)基因的突变会导致一种使人衰弱的X连锁先天性脑发育障碍。在神经元细胞表面,L1可能与多种不同分子相互作用,包括其自身以及免疫球蛋白超家族的另外两种细胞黏附分子(CAMs),即轴突蛋白-1和F11。然而,这些相互作用是否都与正常或异常发育相关尚未确定。超过三分之一的患者突变是单个氨基酸变化,分布在10个细胞外L1结构域中。我们研究了12个错义突变对与L1、轴突蛋白-1和F11结合的影响,并首次表明,虽然许多突变会影响所有三种相互作用,但其他突变仅影响同源或异源结合。因此,患者的病理状况是由于不同类型的L1功能异常所致。突变的性质和功能后果也反映在所得表型的严重程度上,结构突变可能会影响多种结合活性并导致早期死亡。此外,数据表明L1的几个细胞外结构域是同源和异源相互作用所必需的。