Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding

Hum Mutat. 2006 Jun;27(6):599-600. doi: 10.1002/humu.9424.

Abstract

Mutations in the gene encoding dysferlin (DYSF) cause the allelic autosomal recessive disorders limb girdle muscular dystrophy 2B and Miyoshi myopathy. It encompasses 55 exons spanning 150 kb of genomic DNA. Dysferlin is involved in membrane repair in skeletal muscle. We identified three families with novel sequence variants in DYSF. All affected family members showed limb girdle weakness and had reduced or absent dysferlin protein on immunohistochemistry. All exons of DYSF were screened by genomic sequencing. Five novel variants in DYSF were found: two missense mutations (c.895G>A and c.4022T>C), one 5' donor splice-site variant (c.855+1delG), one nonsense mutation (c.1448C>A), and a variant in the 3'UTR of DYSF (c.*107T>A). All alterations were confirmed by restriction enzyme analysis and not found in 400 control alleles. Nonsense mediated RNA decay or changes in the three-dimensional protein structure resulting in intracellular dysferlin aggregates and finally the lack of dysferlin protein were identified as consequences of the novel DYSF variants.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • DNA Mutational Analysis
  • Dysferlin
  • Female
  • Heterozygote
  • Homozygote
  • Humans
  • Male
  • Membrane Proteins / chemistry*
  • Membrane Proteins / deficiency
  • Membrane Proteins / genetics*
  • Models, Molecular
  • Molecular Sequence Data
  • Muscle Proteins / chemistry*
  • Muscle Proteins / deficiency
  • Muscle Proteins / genetics*
  • Muscle, Skeletal / pathology
  • Muscular Dystrophies / diagnosis
  • Muscular Dystrophies / genetics*
  • Mutation*
  • Pedigree
  • Protein Folding
  • Protein Structure, Tertiary
  • RNA Splice Sites
  • RNA Stability
  • RNA, Messenger / metabolism
  • Sequence Alignment

Substances

  • DYSF protein, human
  • Dysferlin
  • Membrane Proteins
  • Muscle Proteins
  • RNA Splice Sites
  • RNA, Messenger