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- W2023658088 endingPage "1249" @default.
- W2023658088 startingPage "1240" @default.
- W2023658088 abstract "Phosphoinositides (PIs) are lipid second messengers implicated in signal transduction and membrane trafficking. Seven distinct PIs can be synthesized by phosphorylation of the inositol ring of phosphatidylinositol (PtdIns), and their metabolism is accurately regulated by PI kinases and phosphatases. Two of the PIs, PtdIns3 P and PtdIns(3,5) P 2 , are present on intracellular endosomal compartments, and several studies suggest that they have a role in membrane remodeling and trafficking. We refer to them as ‘endosomal PIs’. An increasing number of human genetic diseases including myopathy and neuropathies are associated to mutations in enzymes regulating the turnover of these endosomal PIs. The PtdIns3 P and PtdIns(3,5) P 2 3‐phosphatase myotubularin gene is mutated in X‐linked centronuclear myopathy, whereas its homologs MTMR2 and MTMR13 and the PtdIns(3,5) P 2 5‐phosphatase SAC3/FIG4 are implicated in Charcot–Marie–Tooth peripheral neuropathies. Mutations in the gene encoding the PtdIns3 P 5‐kinase PIP5K3/PIKfyve have been found in patients affected with François–Neetens fleck corneal dystrophy. This review presents the roles of the endosomal PIs and their regulators and proposes defects of membrane remodeling as a common pathological mechanism for the corresponding diseases." @default.
- W2023658088 created "2016-06-24" @default.
- W2023658088 creator A5085289587 @default.
- W2023658088 creator A5091621894 @default.
- W2023658088 date "2008-07-15" @default.
- W2023658088 modified "2023-10-14" @default.
- W2023658088 title "Endosomal Phosphoinositides and Human Diseases" @default.
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