[Mutation analysis of beta myosin heavy chain gene in hypertrophic cardiomyopathy families]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):387-92. doi: 10.3760/cma.j.issn.1003-9406.2011.04.006.
[Article in Chinese]

Abstract

Objective: To detect the gene mutations of beta-myosin heavy chain gene (MYH7) in Chinese pedigrees with hypertrophic cardiomyopathy (HCM), and to analyze the correlation between the genotype and phenotype.

Methods: Exons 3, 5, 7-9, 11-16 and 18-23 of the MYH7 gene were amplified with PCR in three Chinese pedigrees with HCM. The products were sequenced. Sequence alignment between the detected and the standard sequences was performed.

Results: A missense mutation of Thr441Met in exon 14 was identified in a pedigree, which was not detected in the controls. Several synonymous mutations of MYH7 gene were detected in the three pedigrees.

Conclusion: The mutation of Thr441Met, located in the actin binding domain of the globular head, was first identified in Chinese. It probably caused HCM. HCM is a heterogeneous disease. Many factors are involved in the process of its occurrence and development.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cardiac Myosins
  • Cardiomyopathy, Hypertrophic / genetics*
  • DNA Mutational Analysis*
  • Female
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Mutation*
  • Myosin Heavy Chains / chemistry
  • Myosin Heavy Chains / genetics*
  • Pedigree*
  • Phenotype

Substances

  • MYH7 protein, human
  • Cardiac Myosins
  • Myosin Heavy Chains