Missense mutation of the β‐cardiac myosin heavy‐chain gene in hypertrophic cardiomyopathy

Abstract

Hypertrophic cardiomyopathy occurs as an autosomal dominant familial disorder or as a sporadic disease without familial involvement. We describe a missense mutation of the β‐cardiac myosin heavy chain (MHC) gene, a G to T transversion (741 Gly→Trp) identified by direct sequencing of exon 20 in four individuals affected with familial hypertrophic cardiomyopathy. Three individuals with sporadic hypertrophic cardiomyopathy, whose parents are clinically and genetically unaffected, had sequence variations of exon 34 of the α‐cardiac MHC gene (a C to T transversion, 1658 Asp→Asp, resulting in FokI site polymorphism), of intron 33 of the α‐cardiac MHC gene (a G to A and an A to T transversion), and also of intron 14 of the β‐cardiac MHC gene (a C to T transversion in a patient with Noonan syndrome). Including our case, 30 missense mutations of the β‐cardiac MHC gene in 49 families have been reported thus far worldwide. Almost all are located in the region of the gene coding for the globular head of the molecule, and only one mutation was found in both Caucasian and Japanese families. Missense mutations of the β‐cardiac MHC gene in hypertrophic cardiomyopathy may therefore differ according to race.