Analysis of Dscam diversity in regulating axon guidance in Drosophila mushroom bodies

被引:178
作者
Zhan, XL
Clemens, JC
Neves, G
Hattori, D
Flanagan, JJ
Hummel, T
Vasconcelos, ML
Chess, A
Zipursky, SL [1 ]
机构
[1] Univ Calif Los Angeles, Howard Hughes Med Inst, Dept Biol Chem, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] MIT, Whitehead Inst Biomed Res, Dept Biol, Cambridge, MA 02142 USA
[3] Univ Munster, Inst Neurobiol, D-48149 Munster, Germany
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.neuron.2004.07.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dscam is an immunoglobulin (Ig) superfamily member that regulates axon guidance and targeting in Drosophila. Alternative splicing potentially generates 38,016 isoforms differing in their extracellular Ig and transmembrane domains. We demonstrate that Dscam mediates the sorting of axons in the developing mushroom body (MB). This correlates with the precise spatiotemporal pattern of Dscam protein expression. We demonstrate that MB neurons express different arrays of Dscam isoforms and that single MB neurons express multiple isoforms. Two different Dscam isoforms differing in their extracellular domains introduced as transgenes into single mutant cells partially rescued the mutant phenotype. Expression of one isoform of Dscam in a cohort of MB neurons induced dominant phenotypes, while expression of a single isoform in a single cell did not. We propose that different extracellular domains of Dscam share a common function and that differences in isoforms expressed on the surface of neighboring axons influence interactions between them.
引用
收藏
页码:673 / 686
页数:14
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