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Lookup NU author(s): Professor Giorgio TascaORCiD
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© 2017 British Neuropathological SocietyAims: Previously, detection of ANO5 protein has been complicated by unspecific antibodies, most of which have not identified the correct protein. The aims of the study were to specify ANO5 protein expression in human skeletal muscle, and to investigate if the ANO5 protein levels are affected by different ANO5 mutations in anoctaminopathy patients. Methods: Four different antibodies were tested for ANO5 specificity. A sample preparation method compatible with membrane proteins, combined with tissue fractionation was used to determine ANO5 expression in cell cultures expressing ANO5, in normal muscles and eight patient biopsies with six different ANO5 mutations in homozygous or compound heterozygous states, and in other dystrophies. Results: Only one specific monoclonal N-terminal ANO5 antibody was efficient in detecting the protein, showing that ANO5 is expressed as a single 107 kD polypeptide in human skeletal muscle. The truncating mutations c.191dupA and c.1261C>T were found to abolish ANO5 expression, whereas the studied point mutations had variable effects; however, all the ANO5 mutations resulted in clearly reduced ANO5 expression in the patient muscle membrane fraction. Attempts to detect ANO5 using immunohistochemistry were not yet successful. Conclusions: The data presented here indicate that the ANO5 protein expression is decreased in ANO5-mutated muscular dystrophy and that most of the non-truncating pathogenic ANO5 mutations likely destabilize the protein and cause its degradation. The method described here allows direct analysis of human ANO5 protein, which can be used in diagnostics, for evaluating the pathogenicity of the potentially harmful ANO5 variants of uncertain significance.
Author(s): Vihola A, Luque H, Savarese M, Penttila S, Lindfors M, Leturcq F, Eymard B, Tasca G, Brais B, Conte T, Charton K, Richard I, Udd B
Publication type: Article
Publication status: Published
Journal: Neuropathology and Applied Neurobiology
Year: 2018
Volume: 44
Issue: 5
Pages: 441-448
Print publication date: 01/08/2018
Online publication date: 10/05/2017
Acceptance date: 10/05/2017
ISSN (print): 0305-1846
ISSN (electronic): 1365-2990
Publisher: Blackwell Publishing Ltd
URL: https://doi.org/10.1111/nan.12410
DOI: 10.1111/nan.12410
PubMed id: 28489263
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