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Restructuring of an asymmetric neural circuit during associative learning

View ORCID ProfileLeo T.H. Tang, View ORCID ProfileGarrett A. Lee, View ORCID ProfileSteven J. Cook, View ORCID ProfileJacquelin Ho, View ORCID ProfileCassandra C. Potter, View ORCID ProfileHannes E. Bülow
doi: https://doi.org/10.1101/2023.01.12.523604
Leo T.H. Tang
1Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
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Garrett A. Lee
1Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
2Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
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Steven J. Cook
2Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
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Jacquelin Ho
2Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
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Cassandra C. Potter
1Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
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Hannes E. Bülow
1Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
2Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, 10461, USA
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  • For correspondence: hannes.buelow@einsteinmed.edu
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Abstract

Asymmetric brain function is common across the animal kingdom and involved in language processing, and likely in learning and memory. What regulates asymmetric brain function remains elusive. Here, we show that the nematode Caenorhabditis elegans restructures an asymmetric salt sensing neural circuit during associative learning. Worms memorize and prefer the salt concentration at which they were raised in the presence of food through a left-biased network architecture. When conditioned at elevated salt concentrations, animals change the left-biased to a right-biased network, which explains the changed salt-seeking behavior. The changes in circuit architecture require new synapse formation induced through asymmetric, paracrine insulin-signaling. Therefore, experience-dependent changes in asymmetric network architecture rely on paracrine insulin signaling and are fundamental to learning and behavior.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted January 13, 2023.
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Restructuring of an asymmetric neural circuit during associative learning
Leo T.H. Tang, Garrett A. Lee, Steven J. Cook, Jacquelin Ho, Cassandra C. Potter, Hannes E. Bülow
bioRxiv 2023.01.12.523604; doi: https://doi.org/10.1101/2023.01.12.523604
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Restructuring of an asymmetric neural circuit during associative learning
Leo T.H. Tang, Garrett A. Lee, Steven J. Cook, Jacquelin Ho, Cassandra C. Potter, Hannes E. Bülow
bioRxiv 2023.01.12.523604; doi: https://doi.org/10.1101/2023.01.12.523604

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