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  Region-Specific Phosphorylation Determines Neuroligin-3 Localization to Excitatory versus Inhibitory Synapses

Altas, B., Tuffy, L. P., Patrizi, A., Dimova, K., Soykan, T., Brandenburg, C., et al. (2023). Region-Specific Phosphorylation Determines Neuroligin-3 Localization to Excitatory versus Inhibitory Synapses. Biological Psychiatry, in press. doi:10.1016/j.biopsych.2023.12.020.

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 Creators:
Altas, Bekir, Author
Tuffy, Liam P.1, Author           
Patrizi, Annarita, Author
Dimova, Kalina1, Author           
Soykan, Tolga1, Author           
Brandenburg, Cheryl, Author
Romanowski, Andrea J., Author
Whitten, Julia R., Author
Robertson, Colin D., Author
Khim, Saovleak N., Author
Crutcher, Garrett W., Author
Ambrozkiewicz, Mateusz1, Author           
Yagensky, Oleksandr2, Author           
Krüger-Burg, Dilja D.1, Author           
Hammer, Matthieu1, Author           
Hsiao, He-Hsuan3, Author           
Laskowski, Pawel R.1, Author           
Dyck, Lydia1, Author           
Puche, Adam C., Author
Sassoè-Pognetto, Marco, Author
Chua, J. J. E.2, Author           Urlaub, Henning3, Author           Jahn, Olaf1, Author           Brose, Nils1, Author                 Poulopoulos, Alexandros1, Author            more..
Affiliations:
1Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society, Göttingen, DE, ou_3350300              
2Emeritus Group Laboratory of Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society, Göttingen, DE, ou_3350145              
3Research Group of Bioanalytical Mass Spectrometry, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society, ou_3350290              

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Free keywords: Neuroligin scaffolding protein phosphorylation inhibitory synapse excitatory synapse autism
 Abstract: Background:
Neuroligin-3 is a postsynaptic adhesion molecule involved in synapse development and function. It is implicated in rare, monogenic forms of autism, and its shedding is critical to the tumor microenvironment of gliomas. While other members of the Neuroligin family exhibit synapse-type specificity in localization and function through distinct interactions with postsynaptic scaffold proteins, the specificity of Neuroligin-3 synaptic localization remains largely unknown.

Methods:
We investigated the synaptic localization of Neuroligin-3 across regions in mouse and human brain samples after validating antibody specificity in knockout animals. We raised a phospho-specific Neuroligin antibody and used phosphoproteomics, cell-based assays, and in utero CRISPR/Cas9 knockout and gene replacement to identify mechanisms that regulate Neuroligin-3 localization to distinct synapse types.

Results:
Neuroligin-3 exhibits region-dependent synapse specificity, largely localizing to excitatory synapses in cortical regions and inhibitory synapses in subcortical regions of the brain in both mice and humans. We identified specific phosphorylation of cortical Neuroligin-3 at a key binding site for recruitment to inhibitory synapses, while subcortical Neuroligin-3 remained unphosphorylated. In vitro, phosphomimetic mutation of that site disrupted Neuroligin-3 association with the inhibitory postsynaptic scaffolding protein, Gephyrin. In vivo, phosphomimetic mutants of Neuroligin-3 localized to excitatory postsynapses, while phospho-null mutants localized to inhibitory postsynapses.

Conclusions:
These data reveal an unexpected region-specific pattern of Neuroligin-3 synapse specificity, as well as a phosphorylation-dependent mechanism that regulates its recruitment to either excitatory or inhibitory synapses. These findings add to our understanding of how Neuroligin-3 is involved in conditions that may affect the balance of excitation and inhibition.

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Language(s): eng - English
 Dates: 2023-12-27
 Publication Status: Published online
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.biopsych.2023.12.020
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Source 1

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Title: Biological Psychiatry
  Other : Biol. Psychiatry
Source Genre: Journal
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Publ. Info: New York : Elsevier
Pages: - Volume / Issue: - Sequence Number: in press Start / End Page: - Identifier: ISSN: 0006-3223
CoNE: https://pure.mpg.de/cone/journals/resource/954925384111