Drosophila Amphiphysin is implicated in protein localization and membrane morphogenesis but not in synaptic vesicle endocytosis

被引:0
|
作者
Zelhof, AC [1 ]
Bao, H
Hardy, RW
Razzaq, A
Zhang, B
Doe, CQ
机构
[1] Univ Oregon 1254, HHMI, Inst Neurosci, Eugene, OR 97403 USA
[2] Univ Texas, Neurobiol Sect, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[3] Univ Calif San Diego, HHMI, Dept Biol, La Jolla, CA 92093 USA
[4] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
[5] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
来源
DEVELOPMENT | 2001年 / 128卷 / 24期
关键词
synapse; postsynaptic density; apical membrane; membrane morphogenesis; Drosophila;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Amphiphysin family members are implicated in synaptic vesicle endocytosis, actin localization and one isoform is an autoantigen in neurological autoimmune disorder; however, there has been no genetic analysis of Amphiphysin function in higher eukaryotes. We show that Drosophila Amphiphysin is localized to actin-rich membrane domains in many cell types, including apical epithelial membranes, the intricately folded apical rhabdomere membranes of photoreceptor neurons and the postsynaptic density of glutamatergic neuromuscular junctions. Flies that lack all Amphiphysin function are viable, lack any observable endocytic defects, but have abnormal localization of the postsynaptic proteins Discs large, Lethal giant larvae and Scribble, altered synaptic physiology, and behavioral defects. Misexpression of Amphiphysin outside its normal membrane domain in photoreceptor neurons results in striking morphological defects. The strong misexpression phenotype coupled with the mild mutant and lack of phenotypes suggests that Amphiphysin acts redundantly with other proteins to organize specialized membrane domains within a diverse array of cell types.
引用
收藏
页码:5005 / 5015
页数:11
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