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1.
bioRxiv ; 2024 Jun 28.
Article in English | MEDLINE | ID: mdl-38895426

ABSTRACT

In most complex nervous systems there is a clear anatomical separation between the nerve cord, which contains most of the final motor outputs necessary for behaviour, and the brain. In insects, the neck connective is both a physical and information bottleneck connecting the brain and the ventral nerve cord (VNC, spinal cord analogue) and comprises diverse populations of descending (DN), ascending (AN) and sensory ascending neurons, which are crucial for sensorimotor signalling and control. Integrating three separate EM datasets, we now provide a complete connectomic description of the ascending and descending neurons of the female nervous system of Drosophila and compare them with neurons of the male nerve cord. Proofread neuronal reconstructions have been matched across hemispheres, datasets and sexes. Crucially, we have also matched 51% of DN cell types to light level data defining specific driver lines as well as classifying all ascending populations. We use these results to reveal the general architecture, tracts, neuropil innervation and connectivity of neck connective neurons. We observe connected chains of descending and ascending neurons spanning the neck, which may subserve motor sequences. We provide a complete description of sexually dimorphic DN and AN populations, with detailed analysis of circuits implicated in sex-related behaviours, including female ovipositor extrusion (DNp13), male courtship (DNa12/aSP22) and song production (AN hemilineage 08B). Our work represents the first EM-level circuit analyses spanning the entire central nervous system of an adult animal.

2.
Nature ; 628(8008): 596-603, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38509371

ABSTRACT

Motor neurons are the final common pathway1 through which the brain controls movement of the body, forming the basic elements from which all movement is composed. Yet how a single motor neuron contributes to control during natural movement remains unclear. Here we anatomically and functionally characterize the individual roles of the motor neurons that control head movement in the fly, Drosophila melanogaster. Counterintuitively, we find that activity in a single motor neuron rotates the head in different directions, depending on the starting posture of the head, such that the head converges towards a pose determined by the identity of the stimulated motor neuron. A feedback model predicts that this convergent behaviour results from motor neuron drive interacting with proprioceptive feedback. We identify and genetically2 suppress a single class of proprioceptive neuron3 that changes the motor neuron-induced convergence as predicted by the feedback model. These data suggest a framework for how the brain controls movements: instead of directly generating movement in a given direction by activating a fixed set of motor neurons, the brain controls movements by adding bias to a continuing proprioceptive-motor loop.


Subject(s)
Drosophila melanogaster , Motor Neurons , Movement , Posture , Proprioception , Animals , Drosophila melanogaster/anatomy & histology , Drosophila melanogaster/genetics , Drosophila melanogaster/physiology , Feedback, Physiological/physiology , Head/physiology , Models, Neurological , Motor Neurons/physiology , Movement/physiology , Posture/physiology , Proprioception/genetics , Proprioception/physiology , Male
3.
Nat Rev Chem ; 7(12): 819-820, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37957368
4.
bioRxiv ; 2023 Jun 01.
Article in English | MEDLINE | ID: mdl-37398009

ABSTRACT

To perform most behaviors, animals must send commands from higher-order processing centers in the brain to premotor circuits that reside in ganglia distinct from the brain, such as the mammalian spinal cord or insect ventral nerve cord. How these circuits are functionally organized to generate the great diversity of animal behavior remains unclear. An important first step in unraveling the organization of premotor circuits is to identify their constituent cell types and create tools to monitor and manipulate these with high specificity to assess their function. This is possible in the tractable ventral nerve cord of the fly. To generate such a toolkit, we used a combinatorial genetic technique (split-GAL4) to create 195 sparse driver lines targeting 198 individual cell types in the ventral nerve cord. These included wing and haltere motoneurons, modulatory neurons, and interneurons. Using a combination of behavioral, developmental, and anatomical analyses, we systematically characterized the cell types targeted in our collection. Taken together, the resources and results presented here form a powerful toolkit for future investigations of neural circuits and connectivity of premotor circuits while linking them to behavioral outputs.

6.
Elife ; 122023 02 23.
Article in English | MEDLINE | ID: mdl-36820523

ABSTRACT

Precise, repeatable genetic access to specific neurons via GAL4/UAS and related methods is a key advantage of Drosophila neuroscience. Neuronal targeting is typically documented using light microscopy of full GAL4 expression patterns, which generally lack the single-cell resolution required for reliable cell type identification. Here, we use stochastic GAL4 labeling with the MultiColor FlpOut approach to generate cellular resolution confocal images at large scale. We are releasing aligned images of 74,000 such adult central nervous systems. An anticipated use of this resource is to bridge the gap between neurons identified by electron or light microscopy. Identifying individual neurons that make up each GAL4 expression pattern improves the prediction of split-GAL4 combinations targeting particular neurons. To this end, we have made the images searchable on the NeuronBridge website. We demonstrate the potential of NeuronBridge to rapidly and effectively identify neuron matches based on morphology across imaging modalities and datasets.


Subject(s)
Drosophila Proteins , Neurosciences , Animals , Drosophila/metabolism , Neurons/metabolism , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Central Nervous System/metabolism , Drosophila melanogaster/genetics , Drosophila melanogaster/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism
7.
Nature ; 613(7944): 534-542, 2023 01.
Article in English | MEDLINE | ID: mdl-36599984

ABSTRACT

To survive, animals must convert sensory information into appropriate behaviours1,2. Vision is a common sense for locating ethologically relevant stimuli and guiding motor responses3-5. How circuitry converts object location in retinal coordinates to movement direction in body coordinates remains largely unknown. Here we show through behaviour, physiology, anatomy and connectomics in Drosophila that visuomotor transformation occurs by conversion of topographic maps formed by the dendrites of feature-detecting visual projection neurons (VPNs)6,7 into synaptic weight gradients of VPN outputs onto central brain neurons. We demonstrate how this gradient motif transforms the anteroposterior location of a visual looming stimulus into the fly's directional escape. Specifically, we discover that two neurons postsynaptic to a looming-responsive VPN type promote opposite takeoff directions. Opposite synaptic weight gradients onto these neurons from looming VPNs in different visual field regions convert localized looming threats into correctly oriented escapes. For a second looming-responsive VPN type, we demonstrate graded responses along the dorsoventral axis. We show that this synaptic gradient motif generalizes across all 20 primary VPN cell types and most often arises without VPN axon topography. Synaptic gradients may thus be a general mechanism for conveying spatial features of sensory information into directed motor outputs.


Subject(s)
Behavior, Animal , Drosophila , Neurons , Psychomotor Performance , Synapses , Animals , Brain/cytology , Brain/physiology , Drosophila/anatomy & histology , Drosophila/cytology , Drosophila/physiology , Neurons/physiology , Visual Fields/physiology , Synapses/metabolism , Axons , Dendrites , Escape Reaction
8.
Curr Biol ; 32(5): 1189-1196.e6, 2022 03 14.
Article in English | MEDLINE | ID: mdl-35090590

ABSTRACT

Similar to many insect species, Drosophila melanogaster is capable of maintaining a stable flight trajectory for periods lasting up to several hours.1,2 Because aerodynamic torque is roughly proportional to the fifth power of wing length,3 even small asymmetries in wing size require the maintenance of subtle bilateral differences in flapping motion to maintain a stable path. Flies can even fly straight after losing half of a wing, a feat they accomplish via very large, sustained kinematic changes to both the damaged and intact wings.4 Thus, the neural network responsible for stable flight must be capable of sustaining fine-scaled control over wing motion across a large dynamic range. In this study, we describe an unusual type of descending neuron (DNg02) that projects directly from visual output regions of the brain to the dorsal flight neuropil of the ventral nerve cord. Unlike many descending neurons, which exist as single bilateral pairs with unique morphology, there is a population of at least 15 DNg02 cell pairs with nearly identical shape. By optogenetically activating different numbers of DNg02 cells, we demonstrate that these neurons regulate wingbeat amplitude over a wide dynamic range via a population code. Using two-photon functional imaging, we show that DNg02 cells are responsive to visual motion during flight in a manner that would make them well suited to continuously regulate bilateral changes in wing kinematics. Collectively, we have identified a critical set of descending neurons that provides the sensitivity and dynamic range required for flight control.


Subject(s)
Drosophila , Flight, Animal , Animals , Biomechanical Phenomena , Drosophila/physiology , Drosophila melanogaster/physiology , Flight, Animal/physiology , Models, Biological , Neurons , Wings, Animal/physiology
9.
Neuron ; 107(6): 1071-1079.e2, 2020 09 23.
Article in English | MEDLINE | ID: mdl-32931755

ABSTRACT

Drosophila melanogaster is an established model for neuroscience research with relevance in biology and medicine. Until recently, research on the Drosophila brain was hindered by the lack of a complete and uniform nomenclature. Recognizing this, Ito et al. (2014) produced an authoritative nomenclature for the adult insect brain, using Drosophila as the reference. Here, we extend this nomenclature to the adult thoracic and abdominal neuromeres, the ventral nerve cord (VNC), to provide an anatomical description of this major component of the Drosophila nervous system. The VNC is the locus for the reception and integration of sensory information and involved in generating most of the locomotor actions that underlie fly behaviors. The aim is to create a nomenclature, definitions, and spatial boundaries for the Drosophila VNC that are consistent with other insects. The work establishes an anatomical framework that provides a powerful tool for analyzing the functional organization of the VNC.


Subject(s)
Drosophila melanogaster/cytology , Ganglia, Invertebrate/cytology , Nerve Net/cytology , Neurons/classification , Terminology as Topic , Animals , Cell Lineage , Drosophila melanogaster/physiology , Ganglia, Invertebrate/physiology , Nerve Net/physiology , Neurons/cytology , Neurons/physiology
10.
Sci Rep ; 9(1): 16604, 2019 11 12.
Article in English | MEDLINE | ID: mdl-31719657

ABSTRACT

Insect olfaction is a suitable model to investigate sensory processing in the brain. Olfactory information is first processed in the antennal lobe and is then conveyed to two second-order centres-the mushroom body calyx and the lateral protocerebrum. Projection neurons processing sex pheromones and plant odours supply the delta area of the inferior lateral protocerebrum (∆ILPC) and lateral horn (LH), respectively. Here, we investigated the neurons arising from these regions in the brain of the silkmoth, Bombyx mori, using mass staining and intracellular recording with a sharp glass microelectrode. The output neurons from the ∆ILPC projected to the superior medial protocerebrum, whereas those from the LH projected to the superior lateral protocerebrum. The dendritic innervations of output neurons from the ∆ILPC formed a subdivision in the ∆ILPC. We discuss pathways for odour processing in higher order centres.


Subject(s)
Bombyx/anatomy & histology , Bombyx/physiology , Cerebrum/physiology , Neurons/physiology , Olfactory Nerve/physiology , Olfactory Pathways/physiology , Animals , Cerebrum/anatomy & histology , Microelectrodes , Neurons/cytology , Olfactory Nerve/anatomy & histology , Olfactory Pathways/anatomy & histology
11.
Nat Neurosci ; 22(7): 1132-1139, 2019 07.
Article in English | MEDLINE | ID: mdl-31182867

ABSTRACT

An approaching predator and self-motion toward an object can generate similar looming patterns on the retina, but these situations demand different rapid responses. How central circuits flexibly process visual cues to activate appropriate, fast motor pathways remains unclear. Here we identify two descending neuron (DN) types that control landing and contribute to visuomotor flexibility in Drosophila. For each, silencing impairs visually evoked landing, activation drives landing, and spike rate determines leg extension amplitude. Critically, visual responses of both DNs are severely attenuated during non-flight periods, effectively decoupling visual stimuli from the landing motor pathway when landing is inappropriate. The flight-dependence mechanism differs between DN types. Octopamine exposure mimics flight effects in one, whereas the other probably receives neuronal feedback from flight motor circuits. Thus, this sensorimotor flexibility arises from distinct mechanisms for gating action-specific descending pathways, such that sensory and motor networks are coupled or decoupled according to the behavioral state.


Subject(s)
Drosophila melanogaster/physiology , Escape Reaction/physiology , Flight, Animal/physiology , Motor Activity/physiology , Neural Pathways/physiology , Neurons/physiology , Psychomotor Performance/physiology , Visual Perception/physiology , Action Potentials , Animals , Efferent Pathways/physiology , Octopamine/pharmacology , Patch-Clamp Techniques , Photic Stimulation
12.
Nat Commun ; 9(1): 3697, 2018 09 12.
Article in English | MEDLINE | ID: mdl-30209268

ABSTRACT

The most fundamental choice an animal has to make when it detects a threat is whether to freeze, reducing its chances of being noticed, or to flee to safety. Here we show that Drosophila melanogaster exposed to looming stimuli in a confined arena either freeze or flee. The probability of freezing versus fleeing is modulated by the fly's walking speed at the time of threat, demonstrating that freeze/flee decisions depend on behavioral state. We describe a pair of descending neurons crucially implicated in freezing. Genetic silencing of DNp09 descending neurons disrupts freezing yet does not prevent fleeing. Optogenetic activation of both DNp09 neurons induces running and freezing in a state-dependent manner. Our findings establish walking speed as a key factor in defensive response choices and reveal a pair of descending neurons as a critical component in the circuitry mediating selection and execution of freezing or fleeing behaviors.


Subject(s)
Drosophila melanogaster/physiology , Escape Reaction/physiology , Animals , Behavior, Animal/physiology , Drosophila melanogaster/genetics , Neurons/metabolism , Optogenetics
13.
Cell Tissue Res ; 374(3): 497-515, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30078100

ABSTRACT

Sex pheromones orient male moths toward conspecific female moths; the presence of visual information modulates this behavior. In the current study, we explore candidate neuronal pathways for the interaction between vision and the locomotor signal for pheromone orientation. We describe the connectivity between visual neuropils and brain premotor centers, the posterior slope (PS) and the lateral accessory lobe (LAL), in the silkmoth Bombyx mori. Using a single-cell labeling technique, we analyze visual projection neurons supplying these areas. Neurons from both the medulla and lobula complex projected to the PS but only the neurons originating in the lobula complex had additional processes to the LAL. Further, we identified populations of putative feedback neurons from the premotor centers to the optic lobe. Neurons originating in the PS were likely to project to the medulla, whereas those originating in the LAL were likely to project to the lobula complex. The anatomical study contributes to further understanding of integration of visual information on the locomotor control in the insect brain.


Subject(s)
Bombyx/anatomy & histology , Motor Cortex/anatomy & histology , Motor Cortex/cytology , Neurons/cytology , Visual Pathways/anatomy & histology , Animals , Feedback , Optic Lobe, Nonmammalian/anatomy & histology
14.
Sci Rep ; 8(1): 9663, 2018 06 25.
Article in English | MEDLINE | ID: mdl-29941958

ABSTRACT

A population of descending neurons connect the brain and thoracic motor center, playing a critical role in controlling behavior. We examined the anatomical organization of descending neurons (DNs) in the brain of the silkmoth Bombyx mori. Moth pheromone orientation is a good model to investigate neuronal mechanisms of behavior. Based on mass staining and single-cell staining, we evaluated the anatomical organization of neurite distribution by DNs in the brain. Dense innervation was observed in the posterior-ventral part of the brain called the posterior slope (PS). We analyzed the morphology of DNs innervating the lateral accessory lobe (LAL), which is considered important for moth olfactory behavior. We observed that all LAL DNs also innervate the PS, suggesting the integration of signals from the LAL and PS. We also identified a set of DNs innervating the PS but not the LAL. These DNs were sensitive to the sex pheromone, suggesting a role of the PS in motor control for pheromone processing. Here we discuss the organization of descending pathways for pheromone orientation.


Subject(s)
Bombyx/cytology , Brain/cytology , Neurons/cytology , Animals , Neurites/metabolism
15.
Elife ; 72018 06 26.
Article in English | MEDLINE | ID: mdl-29943729

ABSTRACT

In most animals, the brain makes behavioral decisions that are transmitted by descending neurons to the nerve cord circuitry that produces behaviors. In insects, only a few descending neurons have been associated with specific behaviors. To explore how descending neurons control an insect's movements, we developed a novel method to systematically assay the behavioral effects of activating individual neurons on freely behaving terrestrial D. melanogaster. We calculated a two-dimensional representation of the entire behavior space explored by these flies, and we associated descending neurons with specific behaviors by identifying regions of this space that were visited with increased frequency during optogenetic activation. Applying this approach across a large collection of descending neurons, we found that (1) activation of most of the descending neurons drove stereotyped behaviors, (2) in many cases multiple descending neurons activated similar behaviors, and (3) optogenetically activated behaviors were often dependent on the behavioral state prior to activation.


Subject(s)
Brain/physiology , Drosophila melanogaster/physiology , Efferent Pathways/physiology , Locomotion/physiology , Neurons/physiology , Spatial Behavior/physiology , Animals , Behavior, Animal , Biological Assay , Brain/anatomy & histology , Brain/cytology , Brain Mapping/methods , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/anatomy & histology , Drosophila melanogaster/cytology , Efferent Pathways/anatomy & histology , Efferent Pathways/cytology , Genes, Reporter , Neurons/cytology , Optogenetics/methods , Transcription Factors/genetics , Transcription Factors/metabolism
16.
Elife ; 72018 06 26.
Article in English | MEDLINE | ID: mdl-29943730

ABSTRACT

In most animals, the brain controls the body via a set of descending neurons (DNs) that traverse the neck. DN activity activates, maintains or modulates locomotion and other behaviors. Individual DNs have been well-studied in species from insects to primates, but little is known about overall connectivity patterns across the DN population. We systematically investigated DN anatomy in Drosophila melanogaster and created over 100 transgenic lines targeting individual cell types. We identified roughly half of all Drosophila DNs and comprehensively map connectivity between sensory and motor neuropils in the brain and nerve cord, respectively. We find the nerve cord is a layered system of neuropils reflecting the fly's capability for two largely independent means of locomotion -- walking and flight -- using distinct sets of appendages. Our results reveal the basic functional map of descending pathways in flies and provide tools for systematic interrogation of neural circuits.


Subject(s)
Brain/physiology , Drosophila melanogaster/physiology , Efferent Pathways/physiology , Locomotion/physiology , Neurons/physiology , Neuropil/physiology , Animals , Animals, Genetically Modified , Brain/anatomy & histology , Brain/cytology , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/anatomy & histology , Drosophila melanogaster/cytology , Genes, Reporter , Neurons/cytology , Neuropil/cytology , Transcription Factors/genetics , Transcription Factors/metabolism
17.
Sci Rep ; 7(1): 14050, 2017 10 25.
Article in English | MEDLINE | ID: mdl-29070905

ABSTRACT

How to wire a neural circuit is crucial for the functioning of the nervous system. Here, we describe the neuroanatomy of the olfactory neurons in the spli mutant strain of silkmoth (Bombyx mori) to investigate the function of a transcription factor involved in neuronal wiring in the central olfactory circuit. The genomic structure of the gene Bmacj6, which encodes a class IV POU domain transcription factor, is disrupted in the spli mutant. We report the neuroanatomical abnormality in the morphology of the antennal lobe projection neurons (PNs) that process the sex pheromone. In addition to the mis-targeting of dendrites and axons, we found axonal bifurcation within the PNs. These results indicate that the morphology of neurons in the pheromone processing pathway is modified by Bmacj6.


Subject(s)
Arthropod Antennae/anatomy & histology , Arthropod Antennae/physiology , Bombyx/physiology , Insect Proteins/metabolism , Neurons/physiology , POU Domain Factors/metabolism , Animals , Axons/chemistry , Axons/physiology , Dendrites/chemistry , Dendrites/physiology , Gene Expression Regulation , Image Processing, Computer-Assisted , Insect Proteins/genetics , Neurons/chemistry , Olfactory Pathways , POU Domain Factors/genetics , Sex Attractants/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism
18.
Neuron ; 94(6): 1190-1204.e6, 2017 Jun 21.
Article in English | MEDLINE | ID: mdl-28641115

ABSTRACT

Animals rely on dedicated sensory circuits to extract and encode environmental features. How individual neurons integrate and translate these features into behavioral responses remains a major question. Here, we identify a visual projection neuron type that conveys predator approach information to the Drosophila giant fiber (GF) escape circuit. Genetic removal of this input during looming stimuli reveals that it encodes angular expansion velocity, whereas other input cell type(s) encode angular size. Motor program selection and timing emerge from linear integration of these two features within the GF. Linear integration improves size detection invariance over prior models and appropriately biases motor selection to rapid, GF-mediated escapes during fast looms. Our findings suggest feature integration, and motor control may occur as simultaneous operations within the same neuron and establish the Drosophila escape circuit as a model system in which these computations may be further dissected at the circuit level. VIDEO ABSTRACT.


Subject(s)
Behavior, Animal/physiology , Brain/physiology , Escape Reaction/physiology , Neurons/physiology , Visual Perception/physiology , Animals , Brain/cytology , Brain/metabolism , Drosophila melanogaster , Immunohistochemistry , Microscopy, Confocal , Neurons/cytology , Neurons/metabolism , Optogenetics , Patch-Clamp Techniques , Probability
19.
J Insect Physiol ; 98: 214-222, 2017 04.
Article in English | MEDLINE | ID: mdl-28118991

ABSTRACT

The neuronal pathways involved in the processing of sex pheromone information were investigated in the hawkmoth Agrius convolvuli (Lepidoptera: Sphingidae), which uses (E,E)-11,13-hexadecadienal (E11,E13-16:Ald) as the single sex pheromone component. We first clarified the anatomical organization of the antennal lobe of A. convolvuli. Subsequently, central neurons in the antennal lobe that responded to E11,E13-16:Ald were identified. The dendritic processes of these neurons were confined within a specific glomerulus (cumulus) in the antennal lobe. The axons of these neurons projected to the inferior lateral protocerebrum and mushroom body calyx. Although the anatomical organization and morphology of individual neurons in A. convolvuli were similar to other species in the superfamily Bombycoidea, the use of cumulus as the single pathway for sex pheromone information processing was characteristic to this species.


Subject(s)
Arthropod Antennae/physiology , Chemotaxis , Moths/physiology , Mushroom Bodies/physiology , Sex Attractants/pharmacology , Animals , Arthropod Antennae/anatomy & histology , Microscopy, Confocal , Moths/anatomy & histology , Mushroom Bodies/anatomy & histology , Neurons/cytology , Neurons/physiology , Olfactory Pathways/anatomy & histology , Olfactory Pathways/physiology
20.
Curr Opin Insect Sci ; 15: 16-26, 2016 06.
Article in English | MEDLINE | ID: mdl-27436728

ABSTRACT

Counterturning is a common movement pattern during orientation behavior in insects. Once male moths sense sex pheromones and then lose the input, they demonstrate zigzag movements, alternating between left and right turns, to increase the probability to contact with the pheromone plume. We summarize the anatomy and function of the neural circuit involved in pheromone orientation in the silkmoth. A neural circuit, the lateral accessory lobe (LAL), serves a role as the circuit module for zigzag movements and controls this operation using a flip-flop neural switch. Circuit design of the LAL is well conserved across species. We hypothesize that this zigzag module is utilized in a wide range of insect behavior. We introduce two examples of the potential use: orientation flight and the waggle dance in bees.


Subject(s)
Bombyx/physiology , Orientation/physiology , Sexual Behavior, Animal/physiology , Animals , Bees/physiology , Male , Pheromones
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