Lee C H, Herman T, Clandinin T R, Lee R, Zipursky S L
Department of Biological Chemistry, Howard Hughes Medical Institute, University of California, Los Angeles, School of Medicine, 5-748 MRL, 675 Charles Young Drive South, Los Angeles, CA 90095, USA.
Neuron. 2001 May;30(2):437-50. doi: 10.1016/s0896-6273(01)00291-4.
Using visual behavioral screens in Drosophila, we identified multiple alleles of N-cadherin. Removal of N-cadherin selectively from photoreceptor neurons (R cells) causes deficits in specific visual behaviors that correlate with disruptions in R cell connectivity. These defects include disruptions in the pattern of neuronal connections made by all three classes of R cells (R1-R6, R7, and R8). N-cadherin is expressed in both R cell axons and their targets. By inducing mitotic recombination in a subclass of eye progenitors, we generated mutant R7 axons surrounded by largely wild-type R cell axons and a wild-type target. R7 axons lacking N-cadherin mistarget to the R8 recipient layer. We consider the implications of these findings in the context of the proposed role for cadherins in target specificity.
利用果蝇的视觉行为筛选,我们鉴定出了N-钙黏蛋白的多个等位基因。从光感受器神经元(R细胞)中选择性去除N-钙黏蛋白会导致特定视觉行为出现缺陷,这些缺陷与R细胞连接性的破坏相关。这些缺陷包括所有三类R细胞(R1-R6、R7和R8)形成的神经元连接模式的破坏。N-钙黏蛋白在R细胞轴突及其靶标中均有表达。通过在眼祖细胞的一个亚类中诱导有丝分裂重组,我们产生了被大量野生型R细胞轴突和野生型靶标包围的突变R7轴突。缺乏N-钙黏蛋白的R7轴突错误靶向到R8受体层。我们在钙黏蛋白在靶标特异性中所提出的作用背景下考虑这些发现的意义。