RGD Reference Report - The phosphoinositide 3-phosphatase MTMR2 interacts with PSD-95 and maintains excitatory synapses by modulating endosomal traffic. - Rat Genome Database

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The phosphoinositide 3-phosphatase MTMR2 interacts with PSD-95 and maintains excitatory synapses by modulating endosomal traffic.

Authors: Lee, HW  Kim, Y  Han, K  Kim, H  Kim, E 
Citation: Lee HW, etal., J Neurosci. 2010 Apr 21;30(16):5508-18. doi: 10.1523/JNEUROSCI.4283-09.2010.
RGD ID: 8553482
Pubmed: PMID:20410104   (View Abstract at PubMed)
PMCID: PMC6632333   (View Article at PubMed Central)
DOI: DOI:10.1523/JNEUROSCI.4283-09.2010   (Journal Full-text)

MTMR2 is a 3-phosphatase specific for the phosphoinositides PI(3)P and PI(3,5)P(2), which are mainly present on endosomes. Mutations in the MTMR2 gene in Schwann cells lead to a severe demyelinating peripheral neuropathy known as Charcot-Marie-Tooth disease type 4B1. MTMR2 expression is also detected in peripheral and central neurons, but neural functions of MTMR2 remain unclear. Here, we report that MTMR2 is localized to excitatory synapses of central neurons via direct interaction with PSD-95, a postsynaptic scaffolding protein abundant at excitatory synapses. Knockdown of MTMR2 in cultured neurons markedly reduces excitatory synapse density and function. This effect is rescued by wild-type MTMR2 but not by a mutant MTMR2 lacking PSD-95 binding or 3-phosphatase activity. MTMR2 knockdown leads to a decrease in the intensity of EEA1-positive early endosomes in dendrites but increases the intensity in the cell body region. Moreover, MTMR2 suppression promotes endocytosis, but not recycling, of the GluR2 subunit of AMPA receptors, which is an endosomal cargo. In addition, colocalization of internalized GluR2 with Lamp1-positive late endosomes/lysosomes is enhanced in the cell body area but not in dendrites. These results suggest that PSD-95-interacting MTMR2 contributes to the maintenance of excitatory synapses by inhibiting excessive endosome formation and destructive endosomal traffic to lysosomes.



Gene Ontology Annotations    Click to see Annotation Detail View

Biological Process

  

Cellular Component

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
Mtmr2Rataxon located_inIDA PMID:20410104BHF-UCL 
Mtmr2Ratcytosol located_inIDA PMID:20410104BHF-UCL 
Lamp1Ratdendrite located_inIDA PMID:20410104BHF-UCL 
Mtmr2Ratdendrite located_inIDA PMID:20410104BHF-UCL 
Mtmr2Ratdendritic spine located_inIDA PMID:20410104BHF-UCL 
Lamp1Ratneuronal cell body located_inIDA PMID:20410104BHF-UCL 
Mtmr2Ratpostsynaptic density located_inIDA PMID:20410104BHF-UCL 
Mtmr2Ratsynaptic membrane located_inIDA PMID:20410104BHF-UCL 
Mtmr2Ratsynaptic vesicle located_inIDA PMID:20410104BHF-UCL 

Molecular Function

  

Objects Annotated

Genes (Rattus norvegicus)
Dlg2  (discs large MAGUK scaffold protein 2)
Dlg3  (discs large MAGUK scaffold protein 3)
Dlg4  (discs large MAGUK scaffold protein 4)
Lamp1  (lysosomal-associated membrane protein 1)
Mtmr2  (myotubularin related protein 2)


Additional Information