[摘要]：The signalling lipid PI(3,5)P-2 is generated on endosomes and regulates retrograde traffic to the trans-Golgi network. Physiological signals regulate rapid, transient changes in PI(3,5)P-2 levels. Mutations that lower PI(3,5)P-2 cause neurodegeneration in human patients and mice. The function of Vac14 in the regulation of PI(3,5)P-2 was uncharacterized previously. Here, we predict that yeast and mammalian Vac14 are composed entirely of HEAT repeats and demonstrate that Vac14 exerts an effect as a scaffold for the PI(3,5)P-2 regulatory complex by direct contact with the known regulators of PI(3,5)P-2: Fig4, Fab1, Vac7 and Atg18. We also report that the mouse mutant ingls (infantile gliosis) results from a missense mutation in Vac14 that prevents the association of Vac14 with Fab1, generating a partial complex. Analysis of ingls and two additional mutants provides insight into the organization of the PI(3,5)P-2 regulatory complex and indicates that Vac14 mediates three distinct mechanisms for the rapid interconversion of PI3P and PI(3,5)P-2. Moreover, these studies show that the association of Fab1 with the complex is essential for viability in the mouse.
