TY - JOUR T1 - A genetic screen for genes that impact peroxisomes in <em>Drosophila</em> identifies candidate genes for human disease JF - bioRxiv DO - 10.1101/704122 SP - 704122 AU - Hillary K. Graves AU - Sharayu Jangam AU - Kai Li Tan AU - Antonella Pignata AU - Elaine S. Seto AU - Shinya Yamamoto AU - Michael F. Wangler Y1 - 2019/01/01 UR - http://biorxiv.org/content/early/2019/07/16/704122.abstract N2 - Peroxisomes are sub-cellular organelles that are essential for proper function of eukaryotic cells. In addition to being the sites of a variety of oxidative reactions, they are crucial regulators of lipid metabolism. Peroxisome loss or dysfunction leads to multisystem diseases in humans that strongly affects the nervous system. In order to uncover previously unidentified genes and mechanisms that impact peroxisomes, we conducted a genetic screen on a collection of lethal mutations on the X chromosome in Drosophila. Using the number, size and morphology of GFP tagged peroxisomes as a readout, we screened for mutations that altered the number and morphology of peroxisomes based on clonal analysis and confocal microscopy. From this screen, we identified 18 genes that cause increases in peroxisome number or altered morphology when mutated. We examined the human homologs of these genes and found that they are involved in a diverse array of cellular processes. Interestingly, the human homologs from the X-chromosome collection are under selective constraint in human populations and are good candidate genes particularly for dominant genetic disease. This in vivo screening approach for peroxisome defects allows identification of novel genes that impact peroxisomes in vivo in a multicellular organism and is a valuable platform to discover genes potentially involved in dominant disease that could affect peroxisomes. ER -