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Drosulfakinin signaling encodes early-life memory for adaptive social plasticity

Jiwon Jeong, Kujin Kwon, Terezia Klaudia Geisseova, Jongbin Lee, View ORCID ProfileTaejoon Kwon, View ORCID ProfileChunghun Lim
doi: https://doi.org/10.1101/2024.04.08.588562
Jiwon Jeong
1Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea
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Kujin Kwon
2Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea
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Terezia Klaudia Geisseova
1Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea
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Jongbin Lee
3Research Center for Cellular Identity, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea
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Taejoon Kwon
2Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea
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  • For correspondence: [email protected] [email protected]
Chunghun Lim
3Research Center for Cellular Identity, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea
4Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea
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  • For correspondence: [email protected] [email protected]
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Abstract

Drosophila establishes social clusters in groups, yet the underlying principles remain poorly understood. Here we performed a systemic analysis of social network behavior (SNB) that quantifies individual social distance (SD) in a group over time. The SNB assessment in 175 inbred strains from the Drosophila Genetics Reference Panel revealed a tight association of short SD with long developmental time, low food intake, and hypoactivity. The developmental inferiority in short-SD individuals was compensated by their group culturing. By contrast, developmental isolation silenced the beneficial effects of social interactions in adults and blunted the plasticity of SNB under physiological challenges. Transcriptome analyses showed genetic diversity for SD traits, whereas social isolation reprogrammed select genetic pathways, regardless of SD phenotypes. In particular, social deprivation suppressed the expression of the neuropeptide Drosulfakinin (Dsk) in three pairs of adult brain neurons. Male-specific DSK signaling to Cholecystokinin-like receptor 17D1 mediated the SNB plasticity. In fact, transgenic manipulations of the DSK signaling were sufficient to imitate the state of social experience. Given the functional conservation of mammalian Dsk homologs, we propose that animals have evolved a dedicated neural mechanism to encode early-life experience and transform group properties adaptively.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://www.ebi.ac.uk/ena/browser/view/PRJEB61423

  • https://github.com/jiunbae/tracking-fly

  • https://github.com/KJKwon/2023_FlyBehavior

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 4.0 International license.
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Posted April 11, 2024.
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Drosulfakinin signaling encodes early-life memory for adaptive social plasticity
Jiwon Jeong, Kujin Kwon, Terezia Klaudia Geisseova, Jongbin Lee, Taejoon Kwon, Chunghun Lim
bioRxiv 2024.04.08.588562; doi: https://doi.org/10.1101/2024.04.08.588562
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Drosulfakinin signaling encodes early-life memory for adaptive social plasticity
Jiwon Jeong, Kujin Kwon, Terezia Klaudia Geisseova, Jongbin Lee, Taejoon Kwon, Chunghun Lim
bioRxiv 2024.04.08.588562; doi: https://doi.org/10.1101/2024.04.08.588562

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