Project: COENZYME Q10 DEFICIENCY SYNDROME: UNDERSTANDING THE GENOTYPE-PHENOTYPE ASSOCIATION AND METABOLIC DYSFUNCTION THROUGH GENERATION OF INDUCED PLURIPOTENT STEM CELLS (iPSCs) FROM PATIENT-SPECIFIC UNCORRECTED AND GENETICALLY-CORRECTED CELLS
Myotubularins (MTMs) define a large family of proteins with several members mutated in different neuromuscular disorders: demyelinating Charcot-Marie-Tooth (CMT) type 4B neuropathies (MTMR2 and MTMR13) and congenital myotubular/centronuclear myopathy (MTM1). These rare diseases are characterized by early onset and abnormal myelination or disorganization of skeletal muscle fibers, respectively. MTM1 and MTMR2 are phospholipid phosphatases acting on PtdIns3P and PtdIns(3,5)P2, known to regulate membrane trafficking. Partners 1 and 2 of this network have previously validated genetic in vitro and in vivo models of the diseases, and they identified several interactors, which have been extensively explored. Despite these findings, however, the cellular events regulated by MTM1 and MTMR2 and whether the phosphatase activity mediates MTM1 and MTMR2 biological function still remain to be clarified. To this aim, we propose: 1) to investigate the MTM1 and MTMR2 sub-cellular localization and dynamics using live cell imaging analysis; 2) to assess whether MTM1 and MTMR2 regulates endosomal membrane trafficking, as suggested by recent findings of partners 1 and 2; 3) to assess the role of the MTM1 and MTMR2 biochemical activity by exploring functional interaction and phenotypic rescue with phosphatases and kinases involved in the PtdIns3P and PtdIns(3,5)P2 metabolism. The three Partners of this network gather the necessary expertises on phospholipid metabolism, muscle and myelination pathology, and on the cell biology of membrane trafficking (Partner 3).
| Acronym | COQ-iPSC |
| Duration | 01/01/2013 - 31/12/2015 |
| Project Topic | 4th JOINT CALL FOR EUROPEAN RESEARCH PROJECTS ON RARE DISEASES (JTC 2012) (Driven by young investigators) |
| Network | E-Rare-2 |
| Call | 4th Joint Call for European Research Projects on Rare Diseases driven by Young Investigators |
Project partner
| Number | Name | Role | Country |
|---|---|---|---|
| 1 | FUNDACION PUBLICA ANDALUZ PROGRESO Y SALUD-Centre of for Genomics and Oncological Research | Coordinator | Spain |
| 2 | The Weizmann Institute of Science | Partner | Israel |
| 3 | Centre Nationale de la Recherche Scientifique (CNRS-INSERM) | Partner | France |