Browse by author
Lookup NU author(s): Professor Christopher Hutchison
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Emery–Dreifuss muscular dystrophy (EDMD) is caused by mutations in the gene encoding the nuclear membrane protein emerin (X-linked EDMD) or in the gene encoding lamins A/C (autosomal dominant EDMD). One hypothesis explaining the disease suggests that the mutations lead to weakness of the nuclear lamina. To test this hypothesis we investigated lamin solubility and distribution in skin fibroblasts from X-EDMD patients. Using in situ extraction of cells and immunofluorescence microscopy or biochemical fractionation and immunoblotting, we found that all lamin subtypes displayed increased solubility properties in fibroblasts from X-EDMD patients compared to normal individuals. Lamin and emerin solubility was mildly increased in fibroblasts from an X-EDMD carrier. Biochemical fractionation and immunoblotting also indicated that lamin C but no other lamin became redistributed from the nuclear lamina to the nucleoplasm in X-EDMD fibroblasts. Indirect immunofluorescence and confocal microscopy studies using lamin A- and lamin C-specific antibodies confirmed that lamin C but not lamin A became redistributed to the nucleoplasm. Interestingly, the lamin A/C binding protein LAP2α was also mislocalized in X-EDMD fibroblasts.
Author(s): Hutchison C; Markiewicz E; Venables R; Alvarez-Reyes M; Quinlan R; Dorobek M; Hausmanowa-Petrucewicz I
Publication type: Article
Publication status: Published
Journal: Journal of Structural Biology
ISSN (print): 1047-8477
ISSN (electronic): 1095-8657
Publisher: Academic Press
Altmetrics provided by Altmetric