A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex

Abstract

Mutations in the gene encoding fukutin related protein (FKRP) produce a spectrum of disease including congenital muscular dystrophy and limb girdle muscular dystrophy. FKRP is one member of a class of molecules thought to be glycosyltransferases that mediate O-linked glycosylation. The primary target of these glycosyltransferases is thought to be dystroglycan. We now report two unrelated Mexican children with congenital muscular dystrophy who each have the identical, novel 1387A > G, N463D mutation. Muscle biopsies from these children show a reduction of α-dystroglycan and also show reduction of β-dystroglycan, and α-, β-, and γ-sarcoglycan, suggesting that FKRP mutations can perturb membrane associated proteins beyond dystroglycan.