| Literature DB >> 25192047 |
David N Herrmann1, Rita Horvath2, Janet E Sowden1, Michael Gonzalez, Michael Gonzales3, Avencia Sanchez-Mejias3, Zhuo Guan4, Roger G Whittaker5, Jorge L Almodovar6, Maria Lane2, Boglarka Bansagi2, Angela Pyle2, Veronika Boczonadi2, Hanns Lochmüller2, Helen Griffin2, Patrick F Chinnery2, Thomas E Lloyd7, J Troy Littleton4, Stephan Zuchner8.
Abstract
Synaptotagmin 2 is a synaptic vesicle protein that functions as a calcium sensor for neurotransmission but has not been previously associated with human disease. Via whole-exome sequencing, we identified heterozygous missense mutations in the C2B calcium-binding domain of the gene encoding Synaptotagmin 2 in two multigenerational families presenting with peripheral motor neuron syndromes. An essential calcium-binding aspartate residue, Asp307Ala, was disrupted by a c.920A>C change in one family that presented with an autosomal-dominant presynaptic neuromuscular junction disorder resembling Lambert-Eaton myasthenic syndrome. A c.923C>T variant affecting an adjacent residue (p.Pro308Leu) produced a presynaptic neuromuscular junction defect and a dominant hereditary motor neuropathy in a second family. Characterization of the mutation homologous to the human c.920A>C variant in Drosophila Synaptotagmin revealed a dominant disruption of synaptic vesicle exocytosis using this transgenic model. These findings indicate that Synaptotagmin 2 regulates neurotransmitter release at human peripheral motor nerve terminals. In addition, mutations in the Synaptotagmin 2 C2B domain represent an important cause of presynaptic congenital myasthenic syndromes and link them with hereditary motor axonopathies.Entities:
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Year: 2014 PMID: 25192047 PMCID: PMC4157148 DOI: 10.1016/j.ajhg.2014.08.007
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025