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Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12
Gladys Montenegro, … , Evan Reid, Stephan Züchner
Gladys Montenegro, … , Evan Reid, Stephan Züchner
Published January 9, 2012
Citation Information: J Clin Invest. 2012;122(2):538-544. https://doi.org/10.1172/JCI60560.
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Research Article Neuroscience

Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

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Abstract

Hereditary spastic paraplegias (HSPs) are a group of genetically heterogeneous neurodegenerative conditions. They are characterized by progressive spastic paralysis of the legs as a result of selective, length-dependent degeneration of the axons of the corticospinal tract. Mutations in 3 genes encoding proteins that work together to shape the ER into sheets and tubules — receptor accessory protein 1 (REEP1), atlastin-1 (ATL1), and spastin (SPAST) — have been found to underlie many cases of HSP in Northern Europe and North America. Applying Sanger and exome sequencing, we have now identified 3 mutations in reticulon 2 (RTN2), which encodes a member of the reticulon family of prototypic ER-shaping proteins, in families with spastic paraplegia 12 (SPG12). These autosomal dominant mutations included a complete deletion of RTN2 and a frameshift mutation predicted to produce a highly truncated protein. Wild-type reticulon 2, but not the truncated protein potentially encoded by the frameshift allele, localized to the ER. RTN2 interacted with spastin, and this interaction required a hydrophobic region in spastin that is involved in ER localization and that is predicted to form a curvature-inducing/sensing hairpin loop domain. Our results directly implicate a reticulon protein in axonopathy, show that this protein participates in a network of interactions among HSP proteins involved in ER shaping, and further support the hypothesis that abnormal ER morphogenesis is a pathogenic mechanism in HSP.

Authors

Gladys Montenegro, Adriana P. Rebelo, James Connell, Rachel Allison, Carla Babalini, Michela D’Aloia, Pasqua Montieri, Rebecca Schüle, Hiroyuki Ishiura, Justin Price, Alleene Strickland, Michael A. Gonzalez, Lisa Baumbach-Reardon, Tine Deconinck, Jia Huang, Giorgio Bernardi, Jeffery M. Vance, Mark T. Rogers, Shoji Tsuji, Peter De Jonghe, Margaret A. Pericak-Vance, Ludger Schöls, Antonio Orlacchio, Evan Reid, Stephan Züchner

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Figure 1

Identification of RTN2 as the SPG12 gene.

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Identification of RTN2 as the SPG12 gene.
   
(A) By candidate gene scre...
(A) By candidate gene screening of the linked chromosomal locus, we identified a mutation in RTN2. A schematic of the RTN2 gene with the corresponding conserved protein domains is drawn to scale. Subsequently, we identified another missense change and a gene deletion. Exons are represented by rectangles. The letters “A,” “B,” “C,” and “D” indicate the location of the copy number variation assays (see D below). TM, transmembrane domain; tel, telomere; cen, centromere. (B) Sanger sequence traces of the identified mutations. The variant nucleotide is highlighted by an “N” in a black rectangle. Fam., family. (C) The missense mutation (S367F) is highly conserved and immediately flanks the transmembrane domain. Letters in lighter font represent not fully conserved amino acids. (D) Four copy number variant assays across the gene (referred to as “A,” “B,” “C,” and “D” on the bars of the graph) identified a patient with a heterozygous loss of RTN2 (green bars). Gray bars indicate samples that had 2 copies of RTN2. The orange bar (X) indicates a control locus on a different chromosome tested in the patient with the RTN2 deletion.

Copyright © 2021 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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