{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Francis D"],"funding":["National Institutes of Health","NIGMS NIH HHS","NIH HHS"],"pagination":["dev200908"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9641670"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["149(19)"],"pubmed_abstract":["Larval terminal cells of the Drosophila tracheal system generate extensive branched tubes, requiring a huge increase in apical membrane. We discovered that terminal cells compromised for apical membrane expansion - mTOR-vATPase axis and apical polarity mutants - were invaded by the neighboring stalk cell. The invading cell grows and branches, replacing the original single intercellular junction between stalk and terminal cell with multiple intercellular junctions. Here, we characterize disjointed, a mutation in the same phenotypic class. We find that disjointed encodes Drosophila Archease, which is required for the RNA ligase (RtcB) function that is essential for tRNA maturation and for endoplasmic reticulum stress-regulated nonconventional splicing of Xbp1 mRNA. We show that the steady-st"],"journal":["Development (Cambridge, England)"],"pubmed_title":["Regulation of Archease by the mTOR-vATPase axis."],"pmcid":["PMC9641670"],"funding_grant_id":["R01 GM089782"],"pubmed_authors":["Burguete AS","Francis D","Ghabrial AS"],"additional_accession":[]},"is_claimable":false,"name":"Regulation of Archease by the mTOR-vATPase axis.","description":"Larval terminal cells of the Drosophila tracheal system generate extensive branched tubes, requiring a huge increase in apical membrane. We discovered that terminal cells compromised for apical membrane expansion - mTOR-vATPase axis and apical polarity mutants - were invaded by the neighboring stalk cell. The invading cell grows and branches, replacing the original single intercellular junction between stalk and terminal cell with multiple intercellular junctions. Here, we characterize disjointed, a mutation in the same phenotypic class. We find that disjointed encodes Drosophila Archease, which is required for the RNA ligase (RtcB) function that is essential for tRNA maturation and for endoplasmic reticulum stress-regulated nonconventional splicing of Xbp1 mRNA. We show that the steady-st","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Oct","modification":"2025-04-26T01:58:55.301Z","creation":"2025-04-06T10:19:47.492Z"},"accession":"S-EPMC9641670","cross_references":{"pubmed":["36111596"],"doi":["10.1242/dev.200908"]}}