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Molecular self-avoidance in synaptic neurexin complexes

Synapses are thought to be organized by interactions of presynaptic neurexins with postsynaptic ligands, particularly with neuroligins and cerebellins. However, when a neuron forms adjacent pre- and postsynaptic specializations, as in dendrodendritic or axo-axonic synapses, nonfunctional cis neurexi...

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Autores principales: Wang, Cosmos Yuqi, Trotter, Justin H., Liakath-Ali, Kif, Lee, Sung-Jin, Liu, Xinran, Südhof, Thomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682996/
https://www.ncbi.nlm.nih.gov/pubmed/34919427
http://dx.doi.org/10.1126/sciadv.abk1924
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author Wang, Cosmos Yuqi
Trotter, Justin H.
Liakath-Ali, Kif
Lee, Sung-Jin
Liu, Xinran
Südhof, Thomas C.
author_facet Wang, Cosmos Yuqi
Trotter, Justin H.
Liakath-Ali, Kif
Lee, Sung-Jin
Liu, Xinran
Südhof, Thomas C.
author_sort Wang, Cosmos Yuqi
collection PubMed
description Synapses are thought to be organized by interactions of presynaptic neurexins with postsynaptic ligands, particularly with neuroligins and cerebellins. However, when a neuron forms adjacent pre- and postsynaptic specializations, as in dendrodendritic or axo-axonic synapses, nonfunctional cis neurexin/ligand interactions would be energetically favored. Here, we reveal an organizational principle for preventing synaptic cis interactions (“self-avoidance”). Using dendrodendritic synapses between mitral and granule cells in the olfactory bulb as a paradigm, we show that, owing to its higher binding affinity, cerebellin-1 blocks the cis interaction of neurexins with neuroligins, thereby enabling trans neurexin/neuroligin interaction. In mitral cells, ablating either cerebellin-1 or neuroligins severely impaired granule cell➔mitral cell synapses, as did overexpression of wild-type neurexins but not of mutant neurexins unable to bind to neuroligins. Our data uncover a molecular interaction network that organizes the self-avoidance of nonfunctional neurexin/ligand cis interactions, thus allowing assembly of physiological trans interactions.
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spelling pubmed-86829962021-12-29 Molecular self-avoidance in synaptic neurexin complexes Wang, Cosmos Yuqi Trotter, Justin H. Liakath-Ali, Kif Lee, Sung-Jin Liu, Xinran Südhof, Thomas C. Sci Adv Neuroscience Synapses are thought to be organized by interactions of presynaptic neurexins with postsynaptic ligands, particularly with neuroligins and cerebellins. However, when a neuron forms adjacent pre- and postsynaptic specializations, as in dendrodendritic or axo-axonic synapses, nonfunctional cis neurexin/ligand interactions would be energetically favored. Here, we reveal an organizational principle for preventing synaptic cis interactions (“self-avoidance”). Using dendrodendritic synapses between mitral and granule cells in the olfactory bulb as a paradigm, we show that, owing to its higher binding affinity, cerebellin-1 blocks the cis interaction of neurexins with neuroligins, thereby enabling trans neurexin/neuroligin interaction. In mitral cells, ablating either cerebellin-1 or neuroligins severely impaired granule cell➔mitral cell synapses, as did overexpression of wild-type neurexins but not of mutant neurexins unable to bind to neuroligins. Our data uncover a molecular interaction network that organizes the self-avoidance of nonfunctional neurexin/ligand cis interactions, thus allowing assembly of physiological trans interactions. American Association for the Advancement of Science 2021-12-17 /pmc/articles/PMC8682996/ /pubmed/34919427 http://dx.doi.org/10.1126/sciadv.abk1924 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Neuroscience
Wang, Cosmos Yuqi
Trotter, Justin H.
Liakath-Ali, Kif
Lee, Sung-Jin
Liu, Xinran
Südhof, Thomas C.
Molecular self-avoidance in synaptic neurexin complexes
title Molecular self-avoidance in synaptic neurexin complexes
title_full Molecular self-avoidance in synaptic neurexin complexes
title_fullStr Molecular self-avoidance in synaptic neurexin complexes
title_full_unstemmed Molecular self-avoidance in synaptic neurexin complexes
title_short Molecular self-avoidance in synaptic neurexin complexes
title_sort molecular self-avoidance in synaptic neurexin complexes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682996/
https://www.ncbi.nlm.nih.gov/pubmed/34919427
http://dx.doi.org/10.1126/sciadv.abk1924
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