Title

VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse.

Document Type

Article

Publication Date

2008

Keywords

Animals, Fetal-Viability, Flavoproteins, Humans, Intracellular-Signaling-Peptides-and-Proteins, Membrane-Proteins, Mice, Mice-Inbred-C57BL, Mice-Inbred-DBA, Mice-Knockout, Models-Biological, Mutation-Missense, Phosphatidylinositol-Phosphates, Phosphatidylinositols, Phosphotransferases-(Alcohol-Group-Acceptor), Protein-Binding, Protein-Interaction-Domains-and-Motifs, Protein-Structure-Secondary, Repetitive-Sequences-Amino-Acid, Saccharomyces-cerevisiae, Saccharomyces-cerevisiae-Proteins, Two-Hybrid-System-Techniques

JAX Source

EMBO J 2008 Dec; 27(24):3221-34.

Abstract

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.