Leighton P A, Mitchell K J, Goodrich L V, Lu X, Pinson K, Scherz P, Skarnes W C, Tessier-Lavigne M
Howard Hughes Medical Institute and Department of Anatomy, University of California, San Francisco, California 94143-0452, USA.
Nature. 2001 Mar 8;410(6825):174-9. doi: 10.1038/35065539.
The search to understand the mechanisms regulating brain wiring has relied on biochemical purification approaches in vertebrates and genetic approaches in invertebrates to identify molecular cues and receptors for axon guidance. Here we describe a phenotype-based gene-trap screen in mice designed for the large-scale identification of genes controlling the formation of the trillions of connections in the mammalian brain. The method incorporates an axonal marker, which helps to identify cell-autonomous mechanisms in axon guidance, and has generated a resource of mouse lines with striking patterns of axonal labelling, which facilitates analysis of the normal wiring diagram of the brain. Studies of two of these mouse lines have identified an in vivo guidance function for a vertebrate transmembrane semaphorin, Sema6A, and have helped re-evaluate that of the Eph receptor EphA4.
为了理解调节大脑神经连接的机制,人们在脊椎动物中采用生物化学纯化方法,在无脊椎动物中采用遗传学方法来识别轴突导向的分子线索和受体。在此,我们描述了一种基于表型的小鼠基因捕获筛选方法,该方法旨在大规模鉴定控制哺乳动物大脑中数万亿连接形成的基因。该方法引入了一种轴突标记物,有助于识别轴突导向中的细胞自主机制,并产生了一批具有显著轴突标记模式的小鼠品系资源,这有助于分析大脑的正常布线图。对其中两个小鼠品系的研究确定了脊椎动物跨膜信号素Sema6A在体内的导向功能,并有助于重新评估Eph受体EphA4的功能。