Identification of a de novo MYH9 mutation in a Chinese family with MYH9-related disease.

OBJECTIVES

MYH9-related disease (MYH9-RD) is a congenital bleeding disorder characterized by thrombocytopenia, platelet macrocytosis, inclusion bodies in neutrophils.The aim of this study was to investigate a Chinese family with MYH9-RD and to identity potential mutations of the MYH9. This investigation will elucidate the molecular mechanisms involved in disease pathogenesis.

METHODS

Whole exome sequencing (WES) followed by Sanger sequencing was conducted on all family members. Multiple bioinformatics tools were programmed to predict the conservation of mutations and the effect on the protein structure, including 3D protein model analysis.

RESULTS

Gene sequencing revealed that the patient carried A de novo missense MYH9 mutation (c.4338T > G, p.Phe1446Leu). Bioinformatics and molecular modeling analyses predict the p.Phe1446Leu variant to be deleterious, with probable disruptive effects on protein structure and consequent functional impairment.

DISCUSSION: Our study suggested that a de novo missense mutation in MYH9 may be causative to MYH9-RD. Furthermore, genetic sequencing is expected to soon become a standard component of the diagnostic evaluation for individuals with platelet disorders.