Version 1
: Received: 6 August 2022 / Approved: 8 August 2022 / Online: 8 August 2022 (10:48:45 CEST)
How to cite:
Brodehl, A.; Holler, S.; Gummert, J.; Milting, H. The N-terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting the Filament Assembly. Preprints2022, 2022080152. https://doi.org/10.20944/preprints202208.0152.v1
Brodehl, A.; Holler, S.; Gummert, J.; Milting, H. The N-terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting the Filament Assembly. Preprints 2022, 2022080152. https://doi.org/10.20944/preprints202208.0152.v1
Brodehl, A.; Holler, S.; Gummert, J.; Milting, H. The N-terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting the Filament Assembly. Preprints2022, 2022080152. https://doi.org/10.20944/preprints202208.0152.v1
APA Style
Brodehl, A., Holler, S., Gummert, J., & Milting, H. (2022). The N-terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting the Filament Assembly. Preprints. https://doi.org/10.20944/preprints202208.0152.v1
Chicago/Turabian Style
Brodehl, A., Jan Gummert and Hendrik Milting. 2022 "The N-terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting the Filament Assembly" Preprints. https://doi.org/10.20944/preprints202208.0152.v1
Abstract
Desmin is the major intermediate filament protein of all three muscle cell types and connects different cell organelles and multi-protein complexes like the cardiac desmosomes. Several pathogenic mutations in the DES gene cause different skeletal and cardiac myopathies. However, the significance of the majority of DES missense variants is currently unknown since functional data are lacking. To determine whether desmin missense mutations within the highly conserved 1A coil domain cause a filament assembly defect, we generated a set of variants with unknown significance and analyzed systematically the filament assembly in transfected SW13 and H9c2 cells using confocal microscopy. We found that mutations in the N-terminal part of the 1A coil domain affect the filament assembly leading to the cytoplasmic desmin aggregation. In contrast, mutant desmin in the C-terminal part of the 1A coil domain form filamentous structures comparable to wild-type desmin. Our findings suggest that the N-terminal part of the 1A coil domain is a hot spot for pathogenic desmin mutations, which affect the desmin filament assembly leading in consequence to skeletal and/or cardiac myopathies. This study may have relevance for the genetic counselling of patients carrying variants in the 1A coil domain of the DES gene.
Biology and Life Sciences, Biochemistry and Molecular Biology
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
