| Literature DB >> 35065713 |
Joseph R Knoedler1, Sayaka Inoue1, Daniel W Bayless1, Taehong Yang1, Adarsh Tantry1, Chung-Ha Davis2, Nicole Y Leung1, Srinivas Parthasarathy3, Grace Wang1, Maricruz Alvarado1, Abbas H Rizvi4, Lief E Fenno1, Charu Ramakrishnan5, Karl Deisseroth6, Nirao M Shah7.
Abstract
Sex hormones exert a profound influence on gendered behaviors. How individual sex hormone-responsive neuronal populations regulate diverse sex-typical behaviors is unclear. We performed orthogonal, genetically targeted sequencing of four estrogen receptor 1-expressing (Esr1+) populations and identified 1,415 genes expressed differentially between sexes or estrous states. Unique subsets of these genes were distributed across all 137 transcriptomically defined Esr1+ cell types, including estrous stage-specific ones, that comprise the four populations. We used differentially expressed genes labeling single Esr1+ cell types as entry points to functionally characterize two such cell types, BNSTprTac1/Esr1 and VMHvlCckar/Esr1. We observed that these two cell types, but not the other Esr1+ cell types in these populations, are essential for sex recognition in males and mating in females, respectively. Furthermore, VMHvlCckar/Esr1 cell type projections are distinct from those of other VMHvlEsr1 cell types. Together, projection and functional specialization of dimorphic cell types enables sex hormone-responsive populations to regulate diverse social behaviors.Entities:
Keywords: aggression; deep sequencing; estrous cycle; maternal behavior; mating; menstrual cycle; sex differences; social behaviors; synaptic plasticity; transcriptomically defined cell types
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Year: 2022 PMID: 35065713 PMCID: PMC8956134 DOI: 10.1016/j.cell.2021.12.031
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582