Lin D M, Goodman C S
Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley 94720.
Neuron. 1994 Sep;13(3):507-23. doi: 10.1016/0896-6273(94)90022-1.
We used the enhancer detection/GAL4 system in Drosophila to direct increased levels of Fasciclin II (Fas II) expression on motoneuron growth cones and axons and to direct ectopic Fas II expression on other cells they encounter. Four classes of abnormal phenotypes are observed: "bypass" phenotypes, in which axons fail to defasciculate at the choice point where they would normally enter their muscle target region and instead extend past their target; "detour" phenotypes, in which these bypass growth cones enter their muscle target region at a different location; "stall" phenotypes, in which axons that enter their muscle target region fail to defasciculate from one another to probe their muscle targets; and "misroute" phenotypes, in which growth cones are diverted onto abnormal pathways by contact with Fas II-positive cells. These phenotypes show that changes in the pattern and level of Fas II expression can alter growth cone guidance, apparently in part by modulating the ability of these growth cones to respond to other guidance cues.
我们利用果蝇中的增强子检测/GAL4系统,使运动神经元生长锥和轴突上的Fasciclin II(Fas II)表达水平升高,并使它们遇到的其他细胞上出现异位Fas II表达。观察到四类异常表型:“绕过”表型,即轴突在正常进入其肌肉靶区的选择点处未能分开,而是越过其靶区延伸;“绕道”表型,即这些绕过的生长锥在不同位置进入其肌肉靶区;“停滞”表型,即进入其肌肉靶区的轴突未能相互分开以探测其肌肉靶标;以及“错误路线”表型,即生长锥通过与Fas II阳性细胞接触而转向异常路径。这些表型表明,Fas II表达模式和水平的变化可以改变生长锥导向,显然部分是通过调节这些生长锥对其他导向线索的反应能力来实现的。