Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia (original) (raw)
- Letter
- Published: 08 February 1990
- Catherine Duff2,
- Francesco Zorzato1,
- Junichi Fujii1,
- Michael Phillips1,
- Robert G. Korneluk3,
- Wanda Frodis4,
- Beverley A. Britt4 &
- …
- Ronald G. Wortont2
Nature volume 343, pages 559–561 (1990)Cite this article
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Abstract
MALIGNANT hyperthermia (MH) is a potentially lethal condition in which sustained muscle contracture, with attendant hypercatabolic reactions and elevation in body temperature, are triggered by commonly used inhalational anaesthetics and skeletal muscle relaxants1. In humans, the trait is usually inherited in an autosomal dominant fashion2, but in halothane-sensitive pigs3with a similar phenotype, inheritance of the disease is autosomal recessive or co-dominant. A simple and accurate non-invasive test for the gene is not available and predisposition to the disease is currently determined through a halothane- and/or caffeine-induced contracture test on a skeletal muscle biopsy4,5. Because Ca2+ is the chief regulator of muscle contraction and metabolism, the primary defect in MH is believed to lie in Ca2+ regulation1,6. Indeed, several studies indicate a defect in the Ca2+ release channel of the sarcoplasmic reticulum7–12, making it a prime candidate for the altered gene product in predisposed individuals. We have recently cloned complementary DNA and genomic DNA encoding the human ryanodine receptor13 (the Ca2+-release channel of the sarcoplasmic reticulum) and mapped the ryanodine receptor gene(RYR) to region q13.1 of human chromosome 19 (ref. 14), in close proximity to genetic markers that have been shown to map near the MH susceptibility locus in humans15 and the halothane-sensitive gene in pigs16. As a more definitive test of whether the RYR gene is a candidate gene for the human MH phenotype, we have carried out a linkage study with MH families to determine whether the MH phenotype segregates with chromosome 19q markers, including markers in the RYR gene. Co-segregation of MH with _RYR_markers, resulting in a lod score of 4.20 at a linkage distance of zero centimorgans, indicates that MH is likely to be caused by mutations in the RYR gene.
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Authors and Affiliations
- Banting and Best Department of Medical Research, Charles H. Best Institute, University of Toronto, 112 College Street, Toronto, Ontario, Canada, M5G 1L6
David H. MacLennan, Francesco Zorzato, Junichi Fujii & Michael Phillips - Department of Genetics, Hospital for Sick Children and Department of Medical Genetics, University of Toronto, 555 University Avenue, Toronto, Ontario, Canada, M5G 1X8
Catherine Duff & Ronald G. Wortont - Division of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada, K1H 8L1
Robert G. Korneluk - Departments of Anaesthesia and Pharmacology, University of Toronto, CCRW-2-834 Toronto General Hospital, 200 Elizabeth Street, Toronto, Ontario, Canada, M5G 2C4
Wanda Frodis & Beverley A. Britt
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- David H. MacLennan
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MacLennan, D., Duff, C., Zorzato, F. et al. Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia.Nature 343, 559–561 (1990). https://doi.org/10.1038/343559a0
- Received: 01 November 1989
- Accepted: 14 December 1989
- Issue Date: 08 February 1990
- DOI: https://doi.org/10.1038/343559a0