Got diversity? Wiring the fly brain with Dscam

被引:56
作者
Zipursky, S. Lawrence [1 ]
Wojtowicz, Woj M. [1 ]
Hattori, Daisuke [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Howard Hughes Med Inst, Dept Biol Chem, Los Angeles, CA 90095 USA
关键词
D O I
10.1016/j.tibs.2006.08.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Drosophila gene Dscam, encoding Down syndrome cell-adhesion molecule, is required for the development of neural circuits. Alternative splicing of Dscam mRNA potentially generates 38 016 isoforms of a cell-surface recognition protein of the immunoglobulin superfamily. These isoforms include 19 008 different ectodomains joined to one of two alternative transmembrane segments. Each ectodomain comprises a unique combination of three variable immunoglobulin domains. Biochemical studies support a model in which each isoform preferentially binds to the same isoform on opposing cell surfaces. This homophilic binding requires matching at all three variable immunoglobulin domains. These findings raise the intriguing possibility that specificity of binding by the Dscam isoforms mediates cell-surface recognition events required for wiring the fly brain.
引用
收藏
页码:581 / 588
页数:8
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