Variants in ASPH cause exertional heat illness and are associated with malignant hyperthermia susceptibility

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作者
Yukari Endo
Linda Groom
Alper Celik
Natalia Kraeva
Chang Seok Lee
Sung Yun Jung
Lois Gardner
Marie-Anne Shaw
Susan L. Hamilton
Philip M. Hopkins
Robert T. Dirksen
Sheila Riazi
James J. Dowling
机构
[1] Hospital for Sick Children,Program for Genetics and Genome Biology
[2] University of Rochester,Department of Physiology
[3] Hospital for Sick Children,Centre for Computation Medicine
[4] Malignant Hyperthermia Unit,Department of Molecular Physiology and Biophysics
[5] Department of Anesthesia,Leeds Institute of Medical Research at St. James’s
[6] Toronto General Hospital,Division of Neurology
[7] Baylor College of Medicine,Department of Paediatrics
[8] University of Leeds,Department of Molecular Genetics
[9] Malignant Hyperthermia Unit,undefined
[10] St. James’s University Hospital,undefined
[11] Hospital for Sick Children,undefined
[12] University of Toronto,undefined
[13] University of Toronto,undefined
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Nature Communications | / 13卷
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摘要
Exertional heat illness (EHI) and malignant hyperthermia (MH) are life threatening conditions associated with muscle breakdown in the setting of triggering factors including volatile anesthetics, exercise, and high environmental temperature. To identify new genetic variants that predispose to EHI and/or MH, we performed genomic sequencing on a cohort with EHI/MH and/or abnormal caffeine-halothane contracture test. In five individuals, we identified rare, pathogenic heterozygous variants in ASPH, a gene encoding junctin, a regulator of excitation-contraction coupling. We validated the pathogenicity of these variants using orthogonal pre-clinical models, CRISPR-edited C2C12 myotubes and transgenic zebrafish. In total, we demonstrate that ASPH variants represent a new cause of EHI and MH susceptibility.
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