<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/GSE334nnn/GSE334949/</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=GSE334949</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Notch Signaling Reprograms Glial Lipid Metabolism to Promote Hypoxia Resistance</name><description>To understand the transcriptional basis of Notch activation-conferred hypoxia tolerance, we performed single-nucleus RNA sequencing (snRNA-seq) of the developing Drosophila central nervous system and generated a comprehensive cellular atlas at single-cell resolution. Analysis of Eaat1-expressing cells revealed that Notch activation reshaped hypoxia-induced transcriptional responses and counteracted metabolic suppression caused by low oxygen. Together, our findings identify Eaat1 glia as a metabolically adaptive glial population and reveal a conserved Notch-regulated mechanism that rewires lipid metabolism to support hypoxia tolerance in the developing brain.</description><dates><publication>2026/06/26</publication></dates><accession>GSE334949</accession><cross_references><GSM>GSM9802556</GSM><GSM>GSM9802555</GSM><GSM>GSM9802554</GSM><GSM>GSM9802553</GSM><GPL>34457</GPL><GSE>334949</GSE><taxon>Drosophila melanogaster</taxon></cross_references></HashMap>