Abstract
Mammalian behaviour and physiology undergo major changes in early life. Young animals rely on conspecifics to meet their needs and start showing nutritional independence and sex-specific social interactions at weaning and puberty, respectively. How neuronal populations regulating homeostatic functions and social behaviours develop during these transitions remains unclear. We used paired transcriptomic and chromatin accessibility profiling to examine the developmental trajectories of neuronal populations in the hypothalamic preoptic region, where cell types with key roles in physiological and behavioural control have been identified1, 2, 3, 4, 5–6. These data show a marked diversity of developmental trajectories shaped by the sex of the animal, and the location and behavioural or physiological function of the corresponding cell types. We identify key stages of preoptic development, including early diversification, perinatal emergence of sex differences, postnatal maturation and refinement of signalling networks, and nonlinear transcriptional changes accelerating at the time of weaning and puberty. We assessed preoptic development in various sensory mutants and find a major role for vomeronasal sensing in the timing of preoptic cell type maturation. These results provide new insights into the development of neurons controlling homeostatic functions and social behaviours and lay ground for examining the dynamics of these functions in early life.
| Original language | English |
|---|---|
| Pages (from-to) | 157-168 |
| Number of pages | 12 |
| Journal | Nature |
| Volume | 647 |
| Issue number | 8088 |
| DOIs | |
| State | Published - Nov 6 2025 |
Bibliographical note
Publisher Copyright:© The Author(s) 2025.
Funding
We thank members of the Dulac laboratory, the Bauer Core Facility, N. Zemke, J. Y. Xiao, D. Bambah-Mukku, W. Allen and J. Chen for helpful advice on experiments, analysis and the manuscript; P. Arter for assistance and D. Di Bella for advice on RNA scope experiments; L. Schwarz for providing Synaptophysin-mGreenLantern-T2A-GAP43-mScarlet AAV; N. Hodgson for help with dark-rearing experiments; S. Butrus for providing data on visual cortex; R. Lang for providing Opn5-cre mice; and R. Hellmiss for help with figures. Illustrations in Fig. 1a created using BioRender (https://biorender.com). T.A.Y. participated in this work through the 2024 Erasmus Mundus Master Programme in Evolutionary Biology (MEME). Work by S.J.H.S. and N.S. was supported in part by Harvard Catalyst | The Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, NIH award UL 1TR002541). This work was supported by Jane Coffin Childs Medical Research Awards grants 61-1749 to H.S.K. and 61-1790 to C.W.S., NIH award K99HD108801 to B.L.L., NIH grant 5UM1HG011585 to B.R. and C.D., NIH grants U19MH114821, R01HD082131 and R01NS112399, and a NOMIS Foundation Award to C.D. C.D. and D.D.G. are investigators at the Howard Hughes Medical Institute. We thank members of the Dulac laboratory, the Bauer Core Facility, N. Zemke, J. Y. Xiao, D. Bambah-Mukku, W. Allen and J. Chen for helpful advice on experiments, analysis and the manuscript; P. Arter for assistance and D. Di Bella for advice on RNA scope experiments; L. Schwarz for providing Synaptophysin-mGreenLantern-T2A-GAP43-mScarlet AAV; N. Hodgson for help with dark-rearing experiments; S. Butrus for providing data on visual cortex; R. Lang for providing Opn5-cre mice; and R. Hellmiss for help with figures. Illustrations in Fig. created using BioRender ( https://biorender.com ). T.A.Y. participated in this work through the 2024 Erasmus Mundus Master Programme in Evolutionary Biology (MEME). Work by S.J.H.S. and N.S. was supported in part by Harvard Catalyst | The Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, NIH award UL 1TR002541). This work was supported by Jane Coffin Childs Medical Research Awards grants 61-1749 to H.S.K. and 61-1790 to C.W.S., NIH award K99HD108801 to B.L.L., NIH grant 5UM1HG011585 to B.R. and C.D., NIH grants U19MH114821, R01HD082131 and R01NS112399, and a NOMIS Foundation Award to C.D. C.D. and D.D.G. are investigators at the Howard Hughes Medical Institute.
| Funders | Funder number |
|---|---|
| Harvard Catalyst | |
| National Center for Advancing Translational Sciences (NCATS) | |
| NOMIS Stiftung | |
| Jane Coffin Childs Memorial Fund for Medical Research | 61-1790, R01NS112399, 61-1749, U19MH114821, R01HD082131, K99HD108801, 5UM1HG011585 |
| National Institutes of Health (NIH) | UL 1TR002541 |
ASJC Scopus subject areas
- General
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