Giovanni Frighetto, Mark Dombrovski, Lesly M Palacios Castillo, Pratap Meera, Parmis S Mirshahidi, Pegah S Mirshahidi, Piero Sanfilippo, Andrea Vaccari, Pratyush Kandimalla, Volker Hartenstein, Yerbol Z Kurmangaliyev, S Lawrence Zipursky, Mark A Frye
{"title":"Electrical synapses mediate visual orientation behavior.","authors":"Giovanni Frighetto, Mark Dombrovski, Lesly M Palacios Castillo, Pratap Meera, Parmis S Mirshahidi, Pegah S Mirshahidi, Piero Sanfilippo, Andrea Vaccari, Pratyush Kandimalla, Volker Hartenstein, Yerbol Z Kurmangaliyev, S Lawrence Zipursky, Mark A Frye","doi":"10.1016/j.cub.2026.09.060","DOIUrl":null,"url":null,"abstract":"<p><p>Animals constantly detect and orient toward salient visual objects, but the neural circuits underlying this process remain poorly understood. We previously showed that T3 neurons, a visual columnar cell type in Drosophila melanogaster, drive saccadic orientation toward visual landmarks during flight. Here, we identify LC17 neurons, a visual projection cell type, as T3 downstream partners for saccadic visual orientation. Using in vivo optical physiology and virtual reality behavior, we demonstrate that LC17 neurons are broadly tuned to visual objects and necessary for object tracking during flight. Notably, this tracking behavior depends on electrical synapses. We show that the innexin Shaking B (ShakB), which forms gap junctions in the fly brain, is highly expressed in LC17 dendrites. Additionally, LC17-specific knockdown of shakB perturbs the cell physiological visual response and impairs the behavioral readout of object motion vision for saccadic orientation. Our findings reveal the mechanisms underlying visual orientation and highlight the interplay between electrical and chemical neurotransmission for object detection and rapid action selection.</p>","PeriodicalId":11359,"journal":{"name":"Current Biology","volume":" ","pages":""},"PeriodicalIF":7.7000,"publicationDate":"2026-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cub.2026.09.060","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Animals constantly detect and orient toward salient visual objects, but the neural circuits underlying this process remain poorly understood. We previously showed that T3 neurons, a visual columnar cell type in Drosophila melanogaster, drive saccadic orientation toward visual landmarks during flight. Here, we identify LC17 neurons, a visual projection cell type, as T3 downstream partners for saccadic visual orientation. Using in vivo optical physiology and virtual reality behavior, we demonstrate that LC17 neurons are broadly tuned to visual objects and necessary for object tracking during flight. Notably, this tracking behavior depends on electrical synapses. We show that the innexin Shaking B (ShakB), which forms gap junctions in the fly brain, is highly expressed in LC17 dendrites. Additionally, LC17-specific knockdown of shakB perturbs the cell physiological visual response and impairs the behavioral readout of object motion vision for saccadic orientation. Our findings reveal the mechanisms underlying visual orientation and highlight the interplay between electrical and chemical neurotransmission for object detection and rapid action selection.
期刊介绍:
Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.