A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures

AbstractDeficiency of the endoplasmic reticulum transmembrane proteinARV1 leads to epileptic encephalopathy in humans and in mice.ARV1 is highly conserved, but its function in human cells is unknown. Studies of yeastarv1 null mutants indicate that it is involved in a number of biochemical processes including the synthesis of sphingolipids and glycosylphosphatidylinositol (GPI), a glycolipid anchor that is attached to the C-termini of many membrane bound proteins. GPI anchors are post-translational modifications, enabling proteins to travel from the endoplasmic reticulum (ER) through the Golgi and to attach to plasma membranes. We identified a homozygous pathogenic mutation inARV1, p.Gly189Arg, in two brothers with infantile encephalopathy, and characterized the biochemical defect caused by this mutation. In addition to reduced expression of ARV1 transcript and protein in patients ’ fibroblasts, complementation tests in yeast showed that theARV1 p.Gly189Arg mutation leads to deficient maturation of Gas1, a GPI-anchored protein, but does not affect sphingolipid synthesis. Our results suggest, that similar to mutations in other proteins in the GPI-anchoring pathway, including PIGM, PIGA, and PIGQ,ARV1 p.Gly189Arg causes a GPI anchoring defect and leads to early onset epileptic encephalopathy.
Source: Neurogenetics - Category: Genetics & Stem Cells Source Type: research