Journal Article

A Novel SIL1 Variant (p.E342K) Associated with Marinesco–Sjögren Syndrome Impairs Protein Stability and Function

Pietrangelo, Laura, Federici, Luca, Viele, Marianna, Valari, Manthoula, Tilemis, Faidon-Nikolaos, Sallese, Michele, Makrythanasis, Periklis, Amodei, Laura, Selenti, Nikoletta, Miele, Adriana Erica, Kampouraki, Afrodite, Del Boccio, Piero, Di Cintio, Federica, Di Marco, Federica, Ruggieri, Anna Giulia, Marinakis, Nikolaos M., Potenza, Francesca

2025

Overview

Marinesco–Sjögren syndrome (MSS) is a rare autosomal recessive neuromuscular disorder marked by ataxia, muscle weakness, cataracts, and often intellectual and skeletal abnormalities. It is commonly caused by loss-of-function variants in the SIL1 gene, which impair binding immunoglobulin protein (BiP) function, leading to protein misfolding and activation of the unfolded protein response. In a 2-year-old patient with typical MSS symptoms, we identified a previously unreported c.1024G>A (p.E342K) variant in SIL1 via whole-exome sequencing. The pathogenicity of this Sil1 variant was supported by evidence of structural changes revealed through in silico predictions, circular dichroism, and native gel electrophoresis. Patient-derived fibroblasts exhibited reduced Sil1 protein levels, likely due to misfolding and degradation, which was partially rescued by proteasome inhibition. Proteomics revealed a profile similar to known MSS cases and a distinctive MSS transcriptional signature. Ultrastructural analysis confirmed typical MSS features, such as autophagic vacuoles and lipid droplets. Although the p.E342K phenotype appears milder than the reference pathogenic variant R111X, our findings support the reclassification of this novel variant as pathogenic, in accordance with the American College of Medical Genetics and Genomics/Association for Molecular Pathology (ACMG/AMP) 2015 guidelines and the refinements proposed by the Clinical Genome Resource Sequence Variant Interpretation (ClinGen SVI) recommendations. Furthermore, the overall evidence also provides important insights into the genotype–phenotype correlation and the underlying pathogenic mechanism of the p.E342K variant.

• Publisher: MDPI AG,Multidisciplinary Digital Publishing Institute (MDPI)
• Subject: Astigmatism / Child, Preschool / Cognition & reasoning / Epilepsy / Exome Sequencing / Female / Fibroblasts / Genotype & phenotype / Guanine Nucleotide Exchange Factors / Humans / Neurodegenerative diseases / Patients / Protein Stability / Proteins / Spinocerebellar Degenerations - genetics / Spinocerebellar Degenerations - metabolism / Spinocerebellar Degenerations - pathology