Tanaka Hideomi, Maeda Ryu, Shoji Wataru, Wada Hironori, Masai Ichiro, Shiraki Toshiyuki, Kobayashi Megumi, Nakayama Ryoko, Okamoto Hitoshi
Laboratory for Developmental Gene Regulation, Brain Science Institute, The Institute of Physical and Chemical Research (RIKEN), 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Development. 2007 Sep;134(18):3259-69. doi: 10.1242/dev.004267. Epub 2007 Aug 15.
In zebrafish embryos, the axons of the posterior trigeminal (Vp) and facial (VII) motoneurons project stereotypically to a small number of target muscles derived from the first and second branchial arches (BA1, BA2). Use of the Islet1 (Isl1)-GFP transgenic line enabled precise real-time observations of the growth cone behaviour of the Vp and VII motoneurons within BA1 and BA2. Screening for N-ethyl-N-nitrosourea-induced mutants identified seven distinct mutations affecting different steps in the axonal pathfinding of these motoneurons. The class 1 mutations caused severe defasciculation and abnormal pathfinding in both Vp and VII motor axons before they reached their target muscles in BA1. The class 2 mutations caused impaired axonal outgrowth of the Vp motoneurons at the BA1-BA2 boundary. The class 3 mutation caused impaired axonal outgrowth of the Vp motoneurons within the target muscles derived from BA1 and BA2. The class 4 mutation caused retraction of the Vp motor axons in BA1 and abnormal invasion of the VII motor axons in BA1 beyond the BA1-BA2 boundary. Time-lapse observations of the class 1 mutant, vermicelli (vmc), which has a defect in the plexin A3 (plxna3) gene, revealed that Plxna3 acts with its ligand Sema3a1 for fasciculation and correct target selection of the Vp and VII motor axons after separation from the common pathways shared with the sensory axons in BA1 and BA2, and for the proper exit and outgrowth of the axons of the primary motoneurons from the spinal cord.
在斑马鱼胚胎中,后三叉神经(Vp)和面神经(VII)运动神经元的轴突以刻板的方式投射到少数源自第一和第二鳃弓(BA1、BA2)的靶肌肉。使用胰岛1(Isl1)-绿色荧光蛋白转基因品系能够精确实时观察BA1和BA2内Vp和VII运动神经元生长锥的行为。对N-乙基-N-亚硝基脲诱导的突变体进行筛选,鉴定出七个不同的突变,这些突变影响这些运动神经元轴突寻路的不同步骤。1类突变在Vp和VII运动轴突到达BA1中的靶肌肉之前,导致严重的轴突束散和异常寻路。2类突变导致Vp运动神经元在BA1-BA2边界处的轴突生长受损。3类突变导致Vp运动神经元在源自BA1和BA2的靶肌肉内的轴突生长受损。4类突变导致BA1中Vp运动轴突回缩,以及BA1中VII运动轴突越过BA1-BA2边界的异常侵入。对1类突变体vermicelli(vmc)进行延时观察,该突变体在丛蛋白A3(plxna3)基因中有缺陷,结果显示,Plxna3与其配体Sema3a1共同作用,在Vp和VII运动轴突与BA1和BA2中感觉轴突共享的共同路径分离后,促进轴突束化和正确的靶标选择,并促进初级运动神经元轴突从脊髓的正确穿出和生长。