Author
Listed:
- Philipp Schlegel
(MRC Laboratory of Molecular Biology
University of Cambridge)
- Yijie Yin
(University of Cambridge)
- Alexander S. Bates
(MRC Laboratory of Molecular Biology
Harvard Medical School
University of Oxford)
- Sven Dorkenwald
(Princeton University
Princeton University)
- Katharina Eichler
(University of Cambridge)
- Paul Brooks
(University of Cambridge)
- Daniel S. Han
(MRC Laboratory of Molecular Biology
University of New South Wales)
- Marina Gkantia
(University of Cambridge)
- Marcia Santos
(University of Cambridge)
- Eva J. Munnelly
(University of Cambridge)
- Griffin Badalamente
(University of Cambridge)
- Laia Serratosa Capdevila
(University of Cambridge)
- Varun A. Sane
(University of Cambridge)
- Alexandra M. C. Fragniere
(University of Cambridge)
- Ladann Kiassat
(University of Cambridge)
- Markus W. Pleijzier
(MRC Laboratory of Molecular Biology)
- Tomke Stürner
(MRC Laboratory of Molecular Biology
University of Cambridge)
- Imaan F. M. Tamimi
(University of Cambridge)
- Christopher R. Dunne
(University of Cambridge)
- Irene Salgarella
(University of Cambridge)
- Alexandre Javier
(University of Cambridge)
- Siqi Fang
(University of Cambridge)
- Eric Perlman
(Yikes)
- Tom Kazimiers
(kazmos)
- Sridhar R. Jagannathan
(University of Cambridge)
- Arie Matsliah
(Princeton University)
- Amy R. Sterling
(Princeton University
Eyewire)
- Szi-chieh Yu
(Princeton University)
- Claire E. McKellar
(Princeton University)
- Marta Costa
(University of Cambridge)
- H. Sebastian Seung
(Princeton University
Princeton University)
- Mala Murthy
(Princeton University)
- Volker Hartenstein
(University of California Los Angeles)
- Davi D. Bock
(University of Vermont)
- Gregory S. X. E. Jefferis
(MRC Laboratory of Molecular Biology
University of Cambridge)
Abstract
The fruit fly Drosophila melanogaster has emerged as a key model organism in neuroscience, in large part due to the concentration of collaboratively generated molecular, genetic and digital resources available for it. Here we complement the approximately 140,000 neuron FlyWire whole-brain connectome1 with a systematic and hierarchical annotation of neuronal classes, cell types and developmental units (hemilineages). Of 8,453 annotated cell types, 3,643 were previously proposed in the partial hemibrain connectome2, and 4,581 are new types, mostly from brain regions outside the hemibrain subvolume. Although nearly all hemibrain neurons could be matched morphologically in FlyWire, about one-third of cell types proposed for the hemibrain could not be reliably reidentified. We therefore propose a new definition of cell type as groups of cells that are each quantitatively more similar to cells in a different brain than to any other cell in the same brain, and we validate this definition through joint analysis of FlyWire and hemibrain connectomes. Further analysis defined simple heuristics for the reliability of connections between brains, revealed broad stereotypy and occasional variability in neuron count and connectivity, and provided evidence for functional homeostasis in the mushroom body through adjustments of the absolute amount of excitatory input while maintaining the excitation/inhibition ratio. Our work defines a consensus cell type atlas for the fly brain and provides both an intellectual framework and open-source toolchain for brain-scale comparative connectomics.
Suggested Citation
Philipp Schlegel & Yijie Yin & Alexander S. Bates & Sven Dorkenwald & Katharina Eichler & Paul Brooks & Daniel S. Han & Marina Gkantia & Marcia Santos & Eva J. Munnelly & Griffin Badalamente & Laia Se, 2024.
"Whole-brain annotation and multi-connectome cell typing of Drosophila,"
Nature, Nature, vol. 634(8032), pages 139-152, October.
Handle:
RePEc:nat:nature:v:634:y:2024:i:8032:d:10.1038_s41586-024-07686-5
DOI: 10.1038/s41586-024-07686-5
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