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| Item Type: | Article |
|---|---|
| Title: | Dysregulated ribonucleoprotein granules impair mitochondrial function in RBM20-related dilated cardiomyopathy |
| Creators: |
Kornienko, Julia  ORCID: https://orcid.org/0000-0002-7876-230X, Müller, Linda H. ORCID: https://orcid.org/0000-0002-9250-0541, Nickel, Alexander ORCID: https://orcid.org/0000-0002-7761-0769, Kohlhaas, Michael ORCID: https://orcid.org/0000-0001-6132-6037, Börmel, Mandy ORCID: https://orcid.org/0000-0002-4354-891X, Alfonso-Gonzalez, Carlos ORCID: https://orcid.org/0009-0001-4307-3352, Oorschot, Viola M.J. ORCID: https://orcid.org/0000-0002-8122-8271, Fungate, Michel, Lewey, Susanne, Kees, Jacob, Müller, Johanna, Lindenhofer, Dominik ORCID: https://orcid.org/0000-0001-8838-7163, Fenzl, Kai ORCID: https://orcid.org/0000-0001-8097-7740, Schraft, Laura ORCID: https://orcid.org/0009-0005-4504-8926, Clauder-Münster, Sandra ORCID: https://orcid.org/0000-0002-9530-2938, Konrad, Laura ORCID: https://orcid.org/0009-0008-4700-7433, Haberkant, Per, Montoya, Frank D.M., Dauksaite, Vita ORCID: https://orcid.org/0000-0002-9399-4731, Gotthardt, Michael ORCID: https://orcid.org/0000-0003-1788-3172, van den Hoogenhof, Maarten M.G. ORCID: https://orcid.org/0000-0003-2768-3457, Maack, Christoph ORCID: https://orcid.org/0000-0003-3694-4559 and Steinmetz, Lars M. ORCID: https://orcid.org/0000-0002-3962-2865
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| Abstract: | BACKGROUND: Pathogenic variants in RBM20 cause severe dilated cardiomyopathy. Loss-of-function variants disrupt splicing; neomorphic gain-of-function (GoF) variants also mislocalize RBM20 to cytoplasmic ribonucleoprotein granules and are associated with more aggressive disease. The mechanism by which RBM20 mislocalization drives cardiac dysfunction remains unknown. METHODS: We investigated the effects of Rbm20 GoF and loss-of-function (LoF) variants using proteomic profiling, protein solubility assays, mitochondrial respiration and calcium flux analyses, and ultrastructural imaging in mouse models. Human induced pluripotent stem cell-derived cardioids were used to validate variant-specific phenotypes. RESULTS: Rbm20 GoF, but not LoF, variants caused posttranscriptional downregulation of soluble mitochondrial proteins, including the calcium efflux regulator TMEM65 (transmembrane protein 65), and reduced solubility of mitochondrial membrane proteins. Electron microscopy revealed enlarged mitochondria with cristae disorganization. Functional assays confirmed impaired oxidative phosphorylation, reduced mitochondrial membrane potential, and abnormal calcium handling in Rbm20 GoF models. Human cardioids reproduced these findings, demonstrating that cytoplasmic mislocalization, rather than splicing deficiency, drives mitochondrial dysfunction. CONCLLUSIONS: Cytoplasmic mislocalization of RBM20 disrupts mitochondrial function by reducing mitochondrial protein abundance, leading to oxidative phosphorylation failure and abnormal mitochondrial calcium handling. This mechanism distinguishes RBM20 GoF from LoF variants and may explain the more severe heart failure phenotype observed in patients with RBM20 GoF variants. These insights advance the mechanistic understanding of RBM20-related cardiomyopathy and identify mitochondrial mRNA/protein regulation as a key node in cardiac energetics. |
| Keywords: | Cardiomyopathy, Dilated, Metabolism, Mitochondria, Heart, Mitochondrial Diseases, Precision Medicine, Ribonucleoproteins, Animals, Mice |
| Source: | Circulation |
| ISSN: | 0009-7322 |
| Publisher: | American Heart Association |
| Date: | 15 September 2026 |
| Official Publication: | https://doi.org/10.1161/circulationaha.125.077061 |
| PubMed: | View item in PubMed |
| Related to: |
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