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Stepwise molecular specification of excitatory synapse diversity on a target neuron

Maëla A. Paul, Séverine M. Sigoillot, Léa Marti, Marine Delagrange, Philippe Mailly, View ORCID ProfileFekrije Selimi
doi: https://doi.org/10.1101/2023.01.03.521946
Maëla A. Paul
1Center for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, Paris, France
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Séverine M. Sigoillot
1Center for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, Paris, France
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Léa Marti
1Center for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, Paris, France
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Marine Delagrange
2Plateforme qPCR-HD-GPC, Institut de Biologie de l’Ecole Normale Supérieure, Paris, France
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Philippe Mailly
1Center for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, Paris, France
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Fekrije Selimi
1Center for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, Paris, France
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  • ORCID record for Fekrije Selimi
  • For correspondence: fekrije.selimi@college-de-france.fr
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Summary

Brain function relies on the generation of a large variety of morphologically and functionally diverse, but specific, neuronal synapses. Here, we show that, initially, synapse formation on a common target neuron, the cerebellar Purkinje cells, involves a presynaptic secreted protein common for all types of excitatory inputs. The molecular program then evolves only in one of the inputs with the additional expression of a combination of presynaptic secreted proteins that specify the mature pattern of connectivity on the target. These results show that some inputs actively and gradually specify their synaptic molecular identity while others rely on the “original code”. Thus, the molecular specification of excitatory synapses, crucial for proper circuit function, is acquired in a stepwise manner during mouse postnatal development and obeys input-specific rules.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • This version of the manuscript has been revised to update all figures and supplemental figures that were on a transparent background and are now on a white background.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted January 12, 2023.
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Stepwise molecular specification of excitatory synapse diversity on a target neuron
Maëla A. Paul, Séverine M. Sigoillot, Léa Marti, Marine Delagrange, Philippe Mailly, Fekrije Selimi
bioRxiv 2023.01.03.521946; doi: https://doi.org/10.1101/2023.01.03.521946
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Stepwise molecular specification of excitatory synapse diversity on a target neuron
Maëla A. Paul, Séverine M. Sigoillot, Léa Marti, Marine Delagrange, Philippe Mailly, Fekrije Selimi
bioRxiv 2023.01.03.521946; doi: https://doi.org/10.1101/2023.01.03.521946

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