{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE322nnn/GSE322512/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Rattus norvegicus"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE322512"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Engrailed-1 Potentiates Mitochondrial Transplant Neuroprotection in Spinal Cord Ischemia-Reperfusion Injury [RNA-Seq]","description":"Spinal cord ischemia-reperfusion injury (SCI/RI) is characterized by severe mitochondrial dysfunction and neuronal apoptosis. The transcription factor Engrailed-1 (En-1) has been identified as a potential regulator of mitochondrial homeostasis and neuroprotection. In this study, we utilized an integrated multi-omics approach to elucidate the molecular mechanisms by which En-1 protects cells from ischemia-like injury. We performed RNA-sequencing (RNA-seq) on PC12 cells with stable En-1 overexpression and their respective controls under both normoxic and oxygen-glucose deprivation/reoxygenation (OGD/R) conditions. To identify direct genomic targets of En-1, Cleavage Under Targets and Tagmentation (CUT&Tag) analysis was conducted. Integration of transcriptomic and DNA-binding profiles revealed a distinct regulatory network through which En-1 modulates mitochondrial function and cell survival. These data provide a comprehensive resource for understanding the transcriptional landscape governed by En-1 and identify potential therapeutic targets for mitigating mitochondrial damage in ischemic neural injuries.","dates":{"publication":"2026/04/17"},"accession":"GSE322512","cross_references":{"GSM":["GSM9553518","GSM9553517"],"GPL":["25947"],"GSE":["322512"],"taxon":["Rattus norvegicus"]}}