Genome-wide analysis reveals novel regulators of synaptic maintenance in Drosophila

被引:1
|
作者
Sidisky, Jessica M. [1 ]
Moreira, Danielle de Paula [1 ]
Okumus, Meryem [1 ]
Caratenuto, Russell [1 ]
Drost, Cassidy [1 ]
Connors, Bali [1 ]
Hussain, Sarrah [1 ]
Alkhatib, Stephanie [1 ]
Babcock, Daniel T. [1 ]
机构
[1] Lehigh Univ, Dept Biol Sci, 111 Res Dr, Bethlehem, PA 18015 USA
基金
美国国家卫生研究院;
关键词
Drosophila; synapse; neuromuscular junction; flight; GENE DISRUPTION PROJECT; MOTOR-NEURON BRANCHES; TRANSGENIC RNAI; NEUROMUSCULAR SYNAPSE; ALZHEIMERS-DISEASE; SEPTATE JUNCTIONS; NATURAL VARIATION; FLIGHT MUSCLES; II RECEPTOR; PROTEIN;
D O I
10.1093/genetics/iyad025
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Maintaining synaptic communication is required to preserve nervous system function as an organism ages. While much work has been accomplished to understand synapse formation and development, we understand relatively little regarding maintaining synaptic integrity throughout aging. To better understand the mechanisms responsible for maintaining synaptic structure and function, we performed an unbiased forward genetic screen to identify genes required for synapse maintenance of adult Drosophila neuromuscular junctions. Using flight behavior as a screening tool, we evaluated flight ability in 198 lines from the Drosophila Genetic Reference Panel to identify single nucleotide polymorphisms (SNPs) that are associated with a progressive loss of flight ability with age. Among the many candidate genes identified from this screen, we focus here on 10 genes with clear human homologs harboring SNPs that are most highly associated with synaptic maintenance. Functional validation of these genes using mutant alleles revealed a progressive loss of synaptic structural integrity. Tissue-specific knockdown of these genes using RNA interference (RNAi) uncovered important roles for these genes in either presynaptic motor neurons, postsynaptic muscles, or associated glial cells, highlighting the importance of each component of tripartite synapses. These results offer greater insight into the mechanisms responsible for maintaining structural and functional integrity of synapses with age.
引用
收藏
页数:19
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