{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE235nnn/GSE235890/"]},"type":"primary"},"statusCodeValue":200,"statusCode":"OK"}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Homo sapiens"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE235890"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Role of mitochondrial RNase P complex in the processing of primary RNA in human mitochondria","description":"The human mitochondrial genome is transcribed into long polycistronic RNA that undergoes subsequent endonucleolytic processing. The role of the mitochondrial RNase P, a protein complex composed of RNA methyltransferase, ribonuclease and dehydrogenase, has been revealed in the processing of the primary mitochondrial RNA. Still, the contribution of catalytic activities of RNase P subunits in the processing of individual processing sites has not been fully described. This study aims to define the role of RNase P subunits in regulating the efficiency of the processing of the primary mitochondrial RNA.","dates":{"publication":"2026/06/27"},"accession":"GSE235890","cross_references":{"GSM":["GSM7511537","GSM7511538"],"GPL":["24676"],"GSE":["235890"],"taxon":["Homo sapiens"]}}