{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Kowada R"],"funding":["Japan Society for the Promotion of Science"],"pagination":["21207"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8551190"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(1)"],"pubmed_abstract":["Synthesis of cytochrome c oxidase (Scox) is a Drosophila homolog of human SCO2 encoding a metallochaperone that transports copper to cytochrome c, and is an essential protein for the assembly of cytochrome c oxidase in the mitochondrial respiratory chain complex. SCO2 is highly conserved in a wide variety of species across prokaryotes and eukaryotes, and mutations in SCO2 are known to cause mitochondrial diseases such as fatal infantile cardioencephalomyopathy, Leigh syndrome, and Charcot-Marie-Tooth disease, a neurodegenerative disorder. These diseases have a common symptom of locomotive dysfunction. However, the mechanisms of their pathogenesis remain unknown, and no fundamental medications or therapies have been established for these diseases. In this study, we demonstrated that the gli"],"journal":["Scientific reports"],"pubmed_title":["The function of Scox in glial cells is essential for locomotive ability in Drosophila."],"pmcid":["PMC8551190"],"funding_grant_id":["JP19K06659","16H06280","Core-to-Core Program, Asia-Africa Science Platforms"],"pubmed_authors":["Lee IS","Okada Y","Kodani A","Yoshida H","Ida H","Kowada R","Yamaguchi M"],"additional_accession":[]},"is_claimable":false,"name":"The function of Scox in glial cells is essential for locomotive ability in Drosophila.","description":"Synthesis of cytochrome c oxidase (Scox) is a Drosophila homolog of human SCO2 encoding a metallochaperone that transports copper to cytochrome c, and is an essential protein for the assembly of cytochrome c oxidase in the mitochondrial respiratory chain complex. SCO2 is highly conserved in a wide variety of species across prokaryotes and eukaryotes, and mutations in SCO2 are known to cause mitochondrial diseases such as fatal infantile cardioencephalomyopathy, Leigh syndrome, and Charcot-Marie-Tooth disease, a neurodegenerative disorder. These diseases have a common symptom of locomotive dysfunction. However, the mechanisms of their pathogenesis remain unknown, and no fundamental medications or therapies have been established for these diseases. In this study, we demonstrated that the gli","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Oct","modification":"2025-04-04T09:38:12.46Z","creation":"2024-10-15T13:12:26.195Z"},"accession":"S-EPMC8551190","cross_references":{"pubmed":["34707123"],"doi":["10.1038/s41598-021-00663-2"]}}