Tucker Ben, Richards Robert I, Lardelli Michael
ARC Special Research Center for the Molecular Genetics of Development and Discipline of Genetics, School of Molecular and Biomedical Science, The University of Adelaide, South Australia, Australia.
Hum Mol Genet. 2006 Dec 1;15(23):3446-58. doi: 10.1093/hmg/ddl422. Epub 2006 Oct 25.
Fragile X Syndrome is a leading heritable cause of mental retardation that results from the loss of FMR1 gene function. Studies in mouse and Drosophila model organisms have been critical in understanding many aspects of the loss of function of the FMR1 gene in the human syndrome. Here, we establish that the zebrafish is a useful model organism for the study of the human fragile X syndrome and can be used to examine phenotypes that are difficult or inaccessible to observation in other model organisms. Using morpholino knockdown of the fmr1 gene, we observed abnormal axonal branching of Rohon-Beard and trigeminal ganglion neurons and guidance and defasciculation defects in the lateral longitudinal fasciculus. We demonstrate that this axonal branching defect can be rescued by treatment with MPEP [2-methyl-6-(phenylethynyl) pyridine]. This is consistent with an interaction between mGluR signalling and fmr1 function in neurite morphogenesis. We also describe novel findings of abnormalities in the abundance of trigeminal ganglion neurons and of craniofacial abnormalities apparently due to dysmorphic cartilage formation. These abnormalities may be related to a role for fmr1 in neural crest cell specification and possibly in migration.
脆性X综合征是智力发育迟缓的主要遗传性病因,由FMR1基因功能丧失所致。对小鼠和果蝇模式生物的研究对于理解人类综合征中FMR1基因功能丧失的诸多方面至关重要。在此,我们证实斑马鱼是研究人类脆性X综合征的有用模式生物,可用于研究在其他模式生物中难以观察或无法观察到的表型。通过使用吗啉代寡核苷酸敲低fmr1基因,我们观察到罗霍恩-比尔神经和三叉神经节神经元的轴突分支异常,以及外侧纵束中的导向和脱束缺陷。我们证明这种轴突分支缺陷可用MPEP [2-甲基-6-(苯乙炔基)吡啶]治疗来挽救。这与代谢型谷氨酸受体信号传导和fmr1功能在神经突形态发生中的相互作用一致。我们还描述了三叉神经节神经元数量异常以及明显由于软骨形成异常导致的颅面异常的新发现。这些异常可能与fmr1在神经嵴细胞特化以及可能在迁移中的作用有关。