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Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons
Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons
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Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons
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Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons
Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons

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Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons
Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons
Journal Article

Comprehensive analysis of the C. elegans connectome reveals novel circuits and functions of previously unstudied neurons

2024
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Overview
Despite decades of research on the Caenorhabditis elegans nervous system based on an anatomical description of synaptic connectivity, the circuits underlying behavior remain incompletely described and the functions of many neurons are still unknown. Updated and more complete chemical and gap junction connectomes of both adult sexes covering the entire animal including the muscle end organ have become available recently. Here, these are analyzed to gain insight into the overall structure of the connectivity network and to suggest functions of individual neuron classes. Modularity analysis divides the connectome graph into 10 communities that can be correlated with broad categories of behavior. A significant role of the body wall musculature end organ is emphasized as both a site of significant information convergence and as a source of sensory input in a feedback loop. Convergence of pathways for multisensory integration occurs throughout the network—most interneurons have similar indegrees and outdegrees and hence disperse information as much as they aggregate it. New insights include description of a set of high degree interneurons connected by many gap junctions running through the ventral cord that may represent a previously unrecognized locus of information processing. There is an apparent mechanosensory and proprioceptive field covering the entire body formed by connectivity of the many mechanosensory neurons of multiple types to 2 interneurons with output connections across the nervous system. Several additional significant, previously unrecognized circuits and pathways are uncovered, some involving unstudied neurons. The insights are valuable for guiding theoretical investigation of network properties as well as experimental studies of the functions of individual neurons, groups of neurons, and circuits.