biostudies-literatureUnknown4(2)Sone M<h4>Background</h4>The subcellular localization of membrane and secreted proteins is finely and dynamically regulated through intracellular vesicular trafficking for permitting various biological processes. Drosophila Amyloid precursor protein like (APPL) and Hikaru genki (HIG) are examples of proteins that show differential subcellular localization among several developmental stages.<h4>Methodology/principal findings</h4>During the study of the localization mechanisms of APPL and HIG, we isolated a novel mutant of the gene, CG1973, which we named yata. This molecule interacted genetically with Appl and is structurally similar to mouse NTKL/SCYL1, whose mutation was reported to cause neurodegeneration. yata null mutants showed phenotypes that included developmental abnormalities, progressiPloS onee4466https://www.ebi.ac.uk/biostudies/studies/S-EPMC2635962biostudies-literatureLoss of yata, a novel gene regulating the subcellular localization of APPL, induces deterioration of neural tissues and lifespan shortening.PMC2635962Sone MAsada MNabeshima YShiwaku HUchida AIbuki IOkazawa HHoshino MKomatsu ASuzuki ETamura TfalseLoss of yata, a novel gene regulating the subcellular localization of APPL, induces deterioration of neural tissues and lifespan shortening.<h4>Background</h4>The subcellular localization of membrane and secreted proteins is finely and dynamically regulated through intracellular vesicular trafficking for permitting various biological processes. Drosophila Amyloid precursor protein like (APPL) and Hikaru genki (HIG) are examples of proteins that show differential subcellular localization among several developmental stages.<h4>Methodology/principal findings</h4>During the study of the localization mechanisms of APPL and HIG, we isolated a novel mutant of the gene, CG1973, which we named yata. This molecule interacted genetically with Appl and is structurally similar to mouse NTKL/SCYL1, whose mutation was reported to cause neurodegeneration. yata null mutants showed phenotypes that included developmental abnormalities, progressi2009-01-01T00:00:00Z20092026-04-07T22:34:35.188Z2019-03-26T23:06:59ZS-EPMC26359621920922610.1371/journal.pone.0004466