High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two malignant hyperthermia susceptible families

Genomics. 1992 Nov;14(3):749-54. doi: 10.1016/s0888-7543(05)80179-x.

Abstract

Malignant hyperthermia susceptibility (MHS) is a potentially lethal, hereditary disorder of skeletal muscle that may be triggered by inhalation anesthetics and depolarizing muscle relaxants. Defects in the gene encoding the ryanodine receptor (RYR1) localized on human chromosome 19q13.1 have been proposed to be responsible for MHS. Using a chromosome 19-specific human/hamster somatic cell hybrid mapping panel, we were able to determine that four closely linked microsatellite repeat markers bracket RYR1 with the order 19cen-D19S75-D19S191-RYR1-(D19S47, D19S190)-19ter. Application of the four markers to genetic studies of MHS showed recombination between the markers and MHS in two families, with linkage analysis apparently excluding the MHS locus from the RYR1 region of 19q13.1. These results therefore support the recent observations of genetic heterogeneity in MHS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 19*
  • Cricetinae
  • DNA, Satellite / genetics*
  • Female
  • Genetic Linkage
  • Genetic Markers
  • Haplotypes
  • Humans
  • Hybrid Cells
  • Male
  • Malignant Hyperthermia / genetics*
  • Molecular Sequence Data
  • Pedigree
  • Receptors, Cholinergic / genetics*
  • Repetitive Sequences, Nucleic Acid*
  • Ryanodine Receptor Calcium Release Channel

Substances

  • DNA, Satellite
  • Genetic Markers
  • Receptors, Cholinergic
  • Ryanodine Receptor Calcium Release Channel