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• W2116373233 abstract "Axonopathies are a group of clinically diverse disorders characterized by the progressive degeneration of the axons of specific neurons. In hereditary spastic paraplegia (HSP), the axons of cortical motor neurons degenerate and cause a spastic movement disorder. HSP is linked to mutations in several loci known collectively as the spastic paraplegia genes (SPGs). We identified a heterozygous receptor accessory protein 1 (REEP1) exon 2 deletion in a patient suffering from the autosomal dominantly inherited HSP variant SPG31. We generated the corresponding mouse model to study the underlying cellular pathology. Mice with heterozygous deletion of exon 2 in Reep1 displayed a gait disorder closely resembling SPG31 in humans. Homozygous exon 2 deletion resulted in the complete loss of REEP1 and a more severe phenotype with earlier onset. At the molecular level, we demonstrated that REEP1 is a neuron-specific, membrane-binding, and membrane curvature–inducing protein that resides in the ER. We further show that Reep1 expression was prominent in cortical motor neurons. In REEP1-deficient mice, these neurons showed reduced complexity of the peripheral ER upon ultrastructural analysis. Our study connects proper neuronal ER architecture to long-term axon survival." @default.
• W2116373233 created "2016-06-24" @default.
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• W2116373233 date "2013-09-24" @default.
• W2116373233 modified "2023-10-17" @default.
• W2116373233 title "A spastic paraplegia mouse model reveals REEP1-dependent ER shaping" @default.
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• W2116373233 doi "https://doi.org/10.1172/jci65665" @default.
• W2116373233 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4038580" @default.
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• W2116373233 hasPublicationYear "2013" @default.
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