| First Author | Turnbull J | Year | 2014 |
| Journal | Ann Neurol | Volume | 75 |
| Issue | 3 | Pages | 442-6 |
| PubMed ID | 24419970 | Mgi Jnum | J:274556 |
| Mgi Id | MGI:6303468 | Doi | 10.1002/ana.24104 |
| Citation | Turnbull J, et al. (2014) PTG protein depletion rescues malin-deficient Lafora disease in mouse. Ann Neurol 75(3):442-6 |
| abstractText | Ubiquitin ligases regulate quantities and activities of target proteins, often pleiotropically. The malin ubiquitin E3 ligase is reported to regulate autophagy, the misfolded protein response, microRNA silencing, Wnt signaling, neuronatin-mediated endoplasmic reticulum stress, and the laforin glycogen phosphatase. Malin deficiency causes Lafora disease, pathologically characterized by neurodegeneration and accumulations of malformed glycogen (Lafora bodies). We show that reducing glycogen production in malin-deficient mice by genetically removing PTG, a glycogen synthesis activator protein, nearly completely eliminates Lafora bodies and rescues the neurodegeneration, myoclonus, seizure susceptibility, and behavioral abnormality. Glycogen synthesis downregulation is a potential therapy for the fatal adolescence onset epilepsy Lafora disease. |
