A conditional strategy for cell-type-specific labeling of endogenous excitatory synapses in Drosophila

被引:5
|
作者
Parisi, Michael J. [1 ]
Aimino, Michael A. [1 ]
Mosca, Timothy J. [1 ]
机构
[1] Thomas Jefferson Univ, Vickie & Jack Farber Inst Neurosci, Dept Neurosci, Bluemle Life Sci Bldg, Philadelphia, PA 19107 USA
来源
CELL REPORTS METHODS | 2023年 / 3卷 / 05期
基金
美国国家卫生研究院;
关键词
TUMOR-SUPPRESSOR GENE; PRESYNAPTIC ACTIVE ZONE; NEUROMUSCULAR-JUNCTION; ANTENNAL LOBE; POSTSYNAPTIC MEMBRANE; SYNAPTIC CONNECTIVITY; LOCAL INTERNEURONS; WIRING SPECIFICITY; OLFACTORY SYSTEM; DISCS-LARGE;
D O I
10.1016/j.crmeth.2023.100477
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chemical neurotransmission occurs at specialized contacts where neurotransmitter release machinery apposes neurotransmitter receptors to underlie circuit function. A series of complex events underlies pre -and postsynaptic protein recruitment to neuronal connections. To better study synaptic development in individual neurons, we need cell-type-specific strategies to visualize endogenous synaptic proteins. Although presynaptic strategies exist, postsynaptic proteins remain less studied because of a paucity of cell-type-specific reagents. To study excitatory postsynapses with cell-type specificity, we engineered dlg1[4K], a conditionally labeled marker of Drosophila excitatory postsynaptic densities. With binary expres-sion systems, dlg1[4K] labels central and peripheral postsynapses in larvae and adults. Using dlg1[4K], we find that distinct rules govern postsynaptic organization in adult neurons, multiple binary expression systems can concurrently label pre-and postsynapse in a cell-type-specific manner, and neuronal DLG1 can some-times localize presynaptically. These results validate our strategy for conditional postsynaptic labeling and demonstrate principles of synaptic organization.
引用
收藏
页数:29
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