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Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

Timothy M. Olson, Virginia V. Michels, Stephen N. Thibodeau, Yin-Shan Tai and Mark T. Keating
Science
New Series, Vol. 280, No. 5364 (May 1, 1998), pp. 750-752
Stable URL: http://www.jstor.org/stable/2895348
Page Count: 3
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Abstract

To test the hypothesis that actin dysfunction leads to heart failure, patients with hereditary idiopathic dilated cardiomyopathy (IDC) were examined for mutations in the cardiac actin gene (ACTC). Missense mutations in ACTC that cosegregate with IDC were identified in two unrelated families. Both mutations affect universally conserved amino acids in domains of actin that attach to Z bands and intercalated discs. Coupled with previous data showing that dystrophin mutations also cause dilated cardiomyopathy, these results raise the possibility that defective transmission of force in cardiac myocytes is a mechanism underlying heart failure.

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