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Architecture of the Mouse Brain Synaptome

Zhu, Fei; Cizeron, M�lissa; Qiu, Zhen; Benavides-Piccione, Ruth; Kopanitsa, Maksym V.; Skene, Nathan G.; Koniaris, Babis; DeFelipe, Javier; Frans�n, Erik; Komiyama, Noboru H.; Grant, Seth G.N.

Authors

Fei Zhu

M�lissa Cizeron

Zhen Qiu

Ruth Benavides-Piccione

Maksym V. Kopanitsa

Nathan G. Skene

Javier DeFelipe

Erik Frans�n

Noboru H. Komiyama

Seth G.N. Grant



Abstract

Synapses are found in vast numbers in the brain and contain complex proteomes. We developed genetic labeling and imaging methods to examine synaptic proteins in individual excitatory synapses across all regions of the mouse brain. Synapse catalogs were generated from the molecular and morphological features of a billion synapses. Each synapse subtype showed a unique anatomical distribution, and each brain region showed a distinct signature of synapse subtypes. Whole-brain synaptome cartography revealed spatial architecture from dendritic to global systems levels and previously unknown anatomical features. Synaptome mapping of circuits showed correspondence between synapse diversity and structural and functional connectomes. Behaviorally relevant patterns of neuronal activity trigger spatiotemporal postsynaptic responses sensitive to the structure of synaptome maps. Areas controlling higher cognitive function contain the greatest synapse diversity, and mutations causing cognitive disorders reorganized synaptome maps. Synaptome technology and resources have wide-ranging application in studies of the normal and diseased brain.

Citation

Zhu, F., Cizeron, M., Qiu, Z., Benavides-Piccione, R., Kopanitsa, M. V., Skene, N. G., …Grant, S. G. (2018). Architecture of the Mouse Brain Synaptome. Neuron, 99(4), 781-799.e10. https://doi.org/10.1016/j.neuron.2018.07.007

Journal Article Type Article
Acceptance Date Jul 3, 2018
Online Publication Date Aug 2, 2018
Publication Date 2018-08
Deposit Date Mar 2, 2020
Publicly Available Date Mar 2, 2020
Journal Neuron
Print ISSN 0896-6273
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 99
Issue 4
Pages 781-799.e10
DOI https://doi.org/10.1016/j.neuron.2018.07.007
Public URL http://researchrepository.napier.ac.uk/Output/2603834

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