Literature DB >> 34912123

Transforming representations of movement from body- to world-centric space.

Amir H Behbahani1, Lydia Hamburg2, Elena A Westeinde3, Jenny Lu3, Paul M Dawson3, Cheng Lyu4, Gaby Maimon4, Michael H Dickinson1, Shaul Druckmann2, Rachel I Wilson5.   

Abstract

When an animal moves through the world, its brain receives a stream of information about the body's translational velocity from motor commands and sensory feedback signals. These incoming signals are referenced to the body, but ultimately, they must be transformed into world-centric coordinates for navigation1,2. Here we show that this computation occurs in the fan-shaped body in the brain of Drosophila melanogaster. We identify two cell types, PFNd and PFNv3-5, that conjunctively encode translational velocity and heading as a fly walks. In these cells, velocity signals are acquired from locomotor brain regions6 and are multiplied with heading signals from the compass system. PFNd neurons prefer forward-ipsilateral movement, whereas PFNv neurons prefer backward-contralateral movement, and perturbing PFNd neurons disrupts idiothetic path integration in walking flies7. Downstream, PFNd and PFNv neurons converge onto hΔB neurons, with a connectivity pattern that pools together heading and translation direction combinations corresponding to the same movement in world-centric space. This network motif effectively performs a rotation of the brain's representation of body-centric translational velocity according to the current heading direction. Consistent with our predictions, we observe that hΔB neurons form a representation of translational velocity in world-centric coordinates. By integrating this representation over time, it should be possible for the brain to form a working memory of the path travelled through the environment8-10.
© 2021. The Author(s), under exclusive licence to Springer Nature Limited.

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Year:  2021        PMID: 34912123     DOI: 10.1038/s41586-021-04191-x

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   69.504


  48 in total

1.  Path integration in desert ants, Cataglyphis fortis.

Authors:  M Müller; R Wehner
Journal:  Proc Natl Acad Sci U S A       Date:  1988-07       Impact factor: 11.205

2.  Idiothetic Path Integration in the Fruit Fly Drosophila melanogaster.

Authors:  Irene S Kim; Michael H Dickinson
Journal:  Curr Biol       Date:  2017-07-20       Impact factor: 10.834

3.  Neuroarchitecture and neuroanatomy of the Drosophila central complex: A GAL4-based dissection of protocerebral bridge neurons and circuits.

Authors:  Tanya Wolff; Nirmala A Iyer; Gerald M Rubin
Journal:  J Comp Neurol       Date:  2014-12-16       Impact factor: 3.215

Review 4.  Neuronal vector coding in spatial cognition.

Authors:  Andrej Bicanski; Neil Burgess
Journal:  Nat Rev Neurosci       Date:  2020-08-06       Impact factor: 34.870

5.  Drosophila re-zero their path integrator at the center of a fictive food patch.

Authors:  Amir H Behbahani; Emily H Palmer; Román A Corfas; Michael H Dickinson
Journal:  Curr Biol       Date:  2021-08-26       Impact factor: 10.834

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

Authors:  Brad K Hulse; Hannah Haberkern; Romain Franconville; Daniel Turner-Evans; Shin-Ya Takemura; Tanya Wolff; Marcella Noorman; Marisa Dreher; Chuntao Dan; Ruchi Parekh; Ann M Hermundstad; Gerald M Rubin; Vivek Jayaraman
Journal:  Elife       Date:  2021-10-26       Impact factor: 8.713

Review 7.  Egocentric and allocentric representations of space in the rodent brain.

Authors:  Cheng Wang; Xiaojing Chen; James J Knierim
Journal:  Curr Opin Neurobiol       Date:  2019-11-30       Impact factor: 6.627

8.  The functional organization of descending sensory-motor pathways in Drosophila.

Authors:  Shigehiro Namiki; Michael H Dickinson; Allan M Wong; Wyatt Korff; Gwyneth M Card
Journal:  Elife       Date:  2018-06-26       Impact factor: 8.140

9.  Distance estimation by foraging honeybees

Authors: 
Journal:  J Exp Biol       Date:  1996       Impact factor: 3.312

10.  Neuroarchitecture of the Drosophila central complex: A catalog of nodulus and asymmetrical body neurons and a revision of the protocerebral bridge catalog.

Authors:  Tanya Wolff; Gerald M Rubin
Journal:  J Comp Neurol       Date:  2018-10-18       Impact factor: 3.215

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  4 in total

Review 1.  From Photons to Behaviors: Neural Implementations of Visual Behaviors in Drosophila.

Authors:  Leesun Ryu; Sung Yong Kim; Anmo J Kim
Journal:  Front Neurosci       Date:  2022-05-04       Impact factor: 5.152

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

Authors:  Brad K Hulse; Hannah Haberkern; Romain Franconville; Daniel Turner-Evans; Shin-Ya Takemura; Tanya Wolff; Marcella Noorman; Marisa Dreher; Chuntao Dan; Ruchi Parekh; Ann M Hermundstad; Gerald M Rubin; Vivek Jayaraman
Journal:  Elife       Date:  2021-10-26       Impact factor: 8.713

3.  Walking strides direct rapid and flexible recruitment of visual circuits for course control in Drosophila.

Authors:  Terufumi Fujiwara; Margarida Brotas; M Eugenia Chiappe
Journal:  Neuron       Date:  2022-05-06       Impact factor: 18.688

4.  A neural circuit for wind-guided olfactory navigation.

Authors:  Andrew M M Matheson; Aaron J Lanz; Ashley M Medina; Al M Licata; Timothy A Currier; Mubarak H Syed; Katherine I Nagel
Journal:  Nat Commun       Date:  2022-08-08       Impact factor: 17.694

  4 in total

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