Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

A. Kimura, H. Harada, J. E. Park, H. Nishi, M. Satoh, M. Takahashi, S. Hiroi, T. Sasaoka, N. Ohbuchi, T. Nakamura, T. Koyanagi, T. H. Hwang, J. A. Choo, K. S. Chung, A. Hasegawa, R. Nagai, O. Okazaki, H. Nakamura, M. Matsuzaki, T. SakamotoH. Toshima, Y. Koga, T. Imaizumi, T. Sasazuki

Research output: Contribution to journalArticlepeer-review

481 Citations (Scopus)


Hypertrophic cardiomyopathy (HCM), the most common cause of sudden death in the young, is an autosomal dominant disease characterized by ventricular hypertrophy accompanied by myofibrillar disarrays. Linkage studies and candidate-gene approaches have demonstrated that about haft of the patients have mutations in one of six disease genes; cardiac β-myosin heavy chain (cβMHC) cardiac troponin T (cTnT), α-tropomyosin (αTM), cardiac myosin binding protein C (cMBP-C), ventricular myosin essential light chain (vMLC1) and ventricular myosin regulatory light chain (vMLC2) genes. Other disease genes remain unknown. Because all the known disease genes encode major contractile elements in cardiac muscle, we have systematically characterized the cardiac sarcomere genes, including cardiac troponin 1 (cTnI), cardiac actin (cACT) and cardiac troponin C (cTnC) in 184 unrelated patients with HCM and found mutations in the cTnI gene in several patients. Family studies showed that an Arg145Gly mutation was linked to HCM and a Lys206Gln mutation had occurred de novo, thus strongly suggesting that cTnI is the seventh HCM gene.

Original languageEnglish
Pages (from-to)379-382
Number of pages4
JournalNature genetics
Issue number4
Publication statusPublished - 1997
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Genetics


Dive into the research topics of 'Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy'. Together they form a unique fingerprint.

Cite this