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A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice.

Rebecca M Boumil | Verity A Letts | Monica C Roberts | Christine Lenz | Connie L Mahaffey | Zhong-Wei Zhang | Tobias Moser | Wayne N Frankel
PLoS genetics | 2010

Dynamin-1 (Dnm1) encodes a large multimeric GTPase necessary for activity-dependent membrane recycling in neurons, including synaptic vesicle endocytosis. Mice heterozygous for a novel spontaneous Dnm1 mutation--fitful--experience recurrent seizures, and homozygotes have more debilitating, often lethal seizures in addition to severe ataxia and neurosensory deficits. Fitful is a missense mutation in an exon that defines the DNM1a isoform, leaving intact the alternatively spliced exon that encodes DNM1b. The expression of the corresponding alternate transcripts is developmentally regulated, with DNM1b expression highest during early neuronal development and DNM1a expression increasing postnatally with synaptic maturation. Mutant DNM1a does not efficiently self-assemble into higher order complexes known to be necessary for proper dynamin function, and it also interferes with endocytic recycling in cell culture. In mice, the mutation results in defective synaptic transmission characterized by a slower recovery from depression after trains of stimulation. The DNM1a and DNM1b isoform pair is highly conserved in vertebrate evolution, whereas invertebrates have only one isoform. We speculate that the emergence of more specialized forms of DNM1 may be important in organisms with complex neuronal function.

Pubmed ID: 20700442

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: R37 NS031348
  • Agency: NINDS NIH HHS, United States
    Id: NS31348
  • Agency: NCI NIH HHS, United States
    Id: P30 CA034196
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS031348
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS064013
  • Agency: NINDS NIH HHS, United States
    Id: R03 NS065255

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