<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE325nnn/GSE325877/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Drosophila melanogaster</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE325877</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Cell-type-specific circadian and light-responsive transcriptional dynamics in adult Drosophila neurons</name><description>The Drosophila adult central brain contains 240 circadian neurons, of which there are more than 25 different neuron subtypes based on connectomic data. Recent single cell RNA-seq (scRNAseq) characterization of these neurons “around the clock” also indicate a similar number of circadian neuron subtypes, but other conclusions from these transcriptomic studies warranted verifying and extending with other approaches. To this end: 1) We used the Drosophila Genetic Reference Panel (DGRP) multiplexing strategy to eliminate 10X batch effects and profile time points together; 2) Large numbers of single nuclei were sequenced (snRNA-seq), which was enabled because the new method EL-INTACT purifies nuclei from frozen heads; 3) We assayed 12 time points under both light–dark (LD) and constant darkness (DD) conditions. These approaches showed dramatic time of day separation of many circadian neuron types and enhanced time-of-day gene expression analysis. The data indicate that most of this regulation is transcriptional and circadian. There were however a small number of light-dependent transcripts, including a few that correspond to mammalian immediate-early genes. They probably play a role in the light-regulation of gene expression and behavior in specific neurons, perhaps circadian entrainment or phase-shifting. The results taken together provide a more comprehensive picture of gene expression heterogeneity within adult Drosophila circadian neurons including how intrinsic clock mechanisms and light cues are integrated across circadian neuron subtypes.</description><dates><publication>2026/08/21</publication></dates><accession>GSE325877</accession><cross_references><GSM>GSM9615957</GSM><GSM>GSM9615956</GSM><GSM>GSM9615958</GSM><GSM>GSM9615955</GSM><GPL>33093</GPL><GSE>325877</GSE><taxon>Drosophila melanogaster</taxon></cross_references></HashMap>