A novel function of neuroligin 3 : Beyond sociality, Regulating lifespan in Drosophila

Neuroligins are conserved postsynaptic adhesion proteins involved in synaptic function and behaviour. In Drosophila melanogaster , Neuroligin 3 (Nlg3) regulates social behaviour, sleep and synaptic architecture. We now report, through analysis of publicly available transcriptomics data, confirmed with RT-qPCR data, that loss-of-function of the nlg3 gene downregulates the expression of longevity-associated genes foxo, hsp70s , and hsp68 . Graded genetic manipulation of the Drosophila melanogaster neuroligin 3 (nlg3) gene indeed modulates both social spacing and lifespan. Specifically, reduced nlg3 expression (via heterozygous deletion, or transposable-element insertion) extends lifespan in both sexes, while overexpression or complete deletion shortens it. In contrast, overexpression or complete loss of nlg3 leads the flies to be further apart (increased social distance, or social space), as does RNAi knockdown, while heterozygous reduction of nlg3 expression either lowers or does not alter the flies social space. This work identifies a previously unrecognized link between a conserved synaptic gene, social behaviour, and organismal longevity.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-10-28
DOI
https://doi.org/10.64898/2026.10.27.762327
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
preprint

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preprint

A novel function of neuroligin 3 : Beyond sociality, Regulating lifespan in Drosophila

Anne F. Simon, Reza Ataei, Judy M Jurbaj
1 links
bioRxiv (Cold Spring Harbor Laboratory)
Genetics, Aging, and Longevity in Model Organisms
preprint

A novel function of neuroligin 3 : Beyond sociality, Regulating lifespan in Drosophila

Anne F. Simon, Reza Ataei, Judy M Jurbaj
preprint en

Abstract

Neuroligins are conserved postsynaptic adhesion proteins involved in synaptic function and behaviour. In Drosophila melanogaster , Neuroligin 3 (Nlg3) regulates social behaviour, sleep and synaptic architecture. We now report, through analysis of publicly available transcriptomics data, confirmed with RT-qPCR data, that loss-of-function of the nlg3 gene downregulates the expression of longevity-associated genes foxo, hsp70s , and hsp68 . Graded genetic manipulation of the Drosophila melanogaster neuroligin 3 (nlg3) gene indeed modulates both social spacing and lifespan. Specifically, reduced nlg3 expression (via heterozygous deletion, or transposable-element insertion) extends lifespan in both sexes, while overexpression or complete deletion shortens it. In contrast, overexpression or complete loss of nlg3 leads the flies to be further apart (increased social distance, or social space), as does RNAi knockdown, while heterozygous reduction of nlg3 expression either lowers or does not alter the flies social space. This work identifies a previously unrecognized link between a conserved synaptic gene, social behaviour, and organismal longevity.

bioRxiv (Cold Spring Harbor Laboratory)
Western University (CA)
Natural Sciences and Engineering Research Council of Canada, National Human Genome Research Institute
Genetics, Aging, and Longevity in Model Organisms
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