Cargando…

A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection

Flexible behaviors over long timescales are thought to engage recurrent neural networks in deep brain regions, which are experimentally challenging to study. In insects, recurrent circuit dynamics in a brain region called the central complex (CX) enable directed locomotion, sleep, and context- and e...

Descripción completa

Detalles Bibliográficos
Autores principales: Hulse, Brad K, Haberkern, Hannah, Franconville, Romain, Turner-Evans, Daniel, Takemura, Shin-ya, Wolff, Tanya, Noorman, Marcella, Dreher, Marisa, Dan, Chuntao, Parekh, Ruchi, Hermundstad, Ann M, Rubin, Gerald M, Jayaraman, Vivek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477501/
https://www.ncbi.nlm.nih.gov/pubmed/34696823
http://dx.doi.org/10.7554/eLife.66039
_version_ 1784790375907459072
author Hulse, Brad K
Haberkern, Hannah
Franconville, Romain
Turner-Evans, Daniel
Takemura, Shin-ya
Wolff, Tanya
Noorman, Marcella
Dreher, Marisa
Dan, Chuntao
Parekh, Ruchi
Hermundstad, Ann M
Rubin, Gerald M
Jayaraman, Vivek
author_facet Hulse, Brad K
Haberkern, Hannah
Franconville, Romain
Turner-Evans, Daniel
Takemura, Shin-ya
Wolff, Tanya
Noorman, Marcella
Dreher, Marisa
Dan, Chuntao
Parekh, Ruchi
Hermundstad, Ann M
Rubin, Gerald M
Jayaraman, Vivek
author_sort Hulse, Brad K
collection PubMed
description Flexible behaviors over long timescales are thought to engage recurrent neural networks in deep brain regions, which are experimentally challenging to study. In insects, recurrent circuit dynamics in a brain region called the central complex (CX) enable directed locomotion, sleep, and context- and experience-dependent spatial navigation. We describe the first complete electron microscopy-based connectome of the Drosophila CX, including all its neurons and circuits at synaptic resolution. We identified new CX neuron types, novel sensory and motor pathways, and network motifs that likely enable the CX to extract the fly’s head direction, maintain it with attractor dynamics, and combine it with other sensorimotor information to perform vector-based navigational computations. We also identified numerous pathways that may facilitate the selection of CX-driven behavioral patterns by context and internal state. The CX connectome provides a comprehensive blueprint necessary for a detailed understanding of network dynamics underlying sleep, flexible navigation, and state-dependent action selection.
format Online
Article
Text
id pubmed-9477501
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-94775012022-09-16 A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection Hulse, Brad K Haberkern, Hannah Franconville, Romain Turner-Evans, Daniel Takemura, Shin-ya Wolff, Tanya Noorman, Marcella Dreher, Marisa Dan, Chuntao Parekh, Ruchi Hermundstad, Ann M Rubin, Gerald M Jayaraman, Vivek eLife Neuroscience Flexible behaviors over long timescales are thought to engage recurrent neural networks in deep brain regions, which are experimentally challenging to study. In insects, recurrent circuit dynamics in a brain region called the central complex (CX) enable directed locomotion, sleep, and context- and experience-dependent spatial navigation. We describe the first complete electron microscopy-based connectome of the Drosophila CX, including all its neurons and circuits at synaptic resolution. We identified new CX neuron types, novel sensory and motor pathways, and network motifs that likely enable the CX to extract the fly’s head direction, maintain it with attractor dynamics, and combine it with other sensorimotor information to perform vector-based navigational computations. We also identified numerous pathways that may facilitate the selection of CX-driven behavioral patterns by context and internal state. The CX connectome provides a comprehensive blueprint necessary for a detailed understanding of network dynamics underlying sleep, flexible navigation, and state-dependent action selection. eLife Sciences Publications, Ltd 2021-10-26 /pmc/articles/PMC9477501/ /pubmed/34696823 http://dx.doi.org/10.7554/eLife.66039 Text en © 2021, Hulse, Haberkern, Franconville et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Hulse, Brad K
Haberkern, Hannah
Franconville, Romain
Turner-Evans, Daniel
Takemura, Shin-ya
Wolff, Tanya
Noorman, Marcella
Dreher, Marisa
Dan, Chuntao
Parekh, Ruchi
Hermundstad, Ann M
Rubin, Gerald M
Jayaraman, Vivek
A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection
title A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection
title_full A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection
title_fullStr A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection
title_full_unstemmed A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection
title_short A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection
title_sort connectome of the drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477501/
https://www.ncbi.nlm.nih.gov/pubmed/34696823
http://dx.doi.org/10.7554/eLife.66039
work_keys_str_mv AT hulsebradk aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT haberkernhannah aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT franconvilleromain aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT turnerevansdaniel aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT takemurashinya aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT wolfftanya aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT noormanmarcella aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT drehermarisa aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT danchuntao aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT parekhruchi aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT hermundstadannm aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT rubingeraldm aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT jayaramanvivek aconnectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT hulsebradk connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT haberkernhannah connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT franconvilleromain connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT turnerevansdaniel connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT takemurashinya connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT wolfftanya connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT noormanmarcella connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT drehermarisa connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT danchuntao connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT parekhruchi connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT hermundstadannm connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT rubingeraldm connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection
AT jayaramanvivek connectomeofthedrosophilacentralcomplexrevealsnetworkmotifssuitableforflexiblenavigationandcontextdependentactionselection