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FLASH GENE
Symbol DYSF contributors: mct/npt/pgu - updated : 23-02-2016
HGNC name dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)
HGNC id 3097
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • seven calcium-dependent C2 binding domains, which are required to promote fusion of intracellular membrane vesicles
  • a C2A domain binding to AHNAK
  • several nuclear membrane targeting sequences, a single transmembrane segment
  • two highly conserved DYSF domains, namely DYSF N in the N-terminus and DYSF C in the C-terminus, with unknown function
  • a short C terminal extracellular tail, that is an apparent binding site for affixin
  • mono polymer dimer
    HOMOLOGY
    interspecies homolog to C.elegans spermatogenesis factor fer-1
    Homologene
    FAMILY
  • dysferlin family
  • CATEGORY structural protein
    SUBCELLULAR LOCALIZATION     plasma membrane
        intracellular
    intracellular,cytoplasm,organelle,membrane
    intracellular,cytoplasm,organelle,endoplasmic reticulum
    intracellular,cytoplasm,organelle,Golgi
    intracellular,cytoplasm,cytosolic,vesicle
    text
  • in normal skeletal muscle, dysferlin and AHNAK colocalize at the sarcolemmal membrane and T-tubules
  • abundant dysferlin expression in the Golgi apparatus, around the perinuclear region and to a lesser extent in the nucleus of endothelial cells
  • basic FUNCTION
  • involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events
  • involved in membrane regeneration and repair (first member of the membrane repair machinery in skeletal muscle)
  • implicated in calcium-dependent membrane repair
  • participates in the recruitment and stabilization of AHNAK to the sarcolemma
  • involved in efficient and active membrane repair system to overcome the rigours of frequent contraction of the muscles
  • is necessary for correct T-tubule formation, and dysferlin-deficient skeletal muscle is characterized by abnormally configured T-tubules
  • role for the muscle repair protein dysferlin in endothelial cell adhesion and angiogenesis
  • ferlins are calcium-sensing proteins and are candidate mediators of vesicle-plasma membrane fusion during myoblast fusion
  • membrane-anchored protein known to facilitate membrane repair in skeletal muscles following mechanical injury
  • not only mediates membrane repair but also trafficking of client proteins, ultimately, help bridging dysferlinopathies to aberrant membrane signaling
  • indirectly regulates the membrane expression of proteins by trafficking the lipid patches/vesicles that contain membrane proteins, rather than binding directly the cargo proteins
  • multi-C2 domain transmembrane protein involved in skeletal muscle membrane repair, but also in myogenesis, cellular adhesion and intercellular calcium signaling
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
  • CAPN3/DYSF
  • DYSF dimerization is mediated by its transmembrane domain and by multiple C2 domains
  • RIPOR2 is an essential component of the HDAC6-dysferlin complex
  • INTERACTION
    DNA
    RNA
    small molecule
    protein
  • CAPN3
  • CAV3 (putative low affinity process)and CAV1 (caveolins are essential for dysferlin association with the plasma membrane)
  • interacting with other dysferlin molecules and annexins A1 and A2 at the sarcolemma
  • interacting with PARVB
  • interacts with alpha-tubulin and microtubules in muscle cells
  • ferlins and EHBP1 may compete for EHD binding to regulate the complex process of exit from the endocytic recycling compartment, translocation to the plasma membrane, and reorganization of the actin cytoskeleton to facilitate the fusion of exocytosed vesicles to the membrane
  • HDAC6 is a novel dysferlin-binding partner(DYSF prevents HDAC6 from deacetylating alpha-tubulin by physically binding to both the enzyme, via its C2D domain, and to the substrate, alpha-tubulin, via its C2A and C2B domains)
  • DYSF interacts with CASQ1, MYOM2 and dynein in human skeletal muscle
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) DMAT , LGMD2B , MMD1
    related resource Limb-Girdle Muscular Dystrophy ,type 2B
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    neuromuscularmyopathy 
    enhancement of the neutrophil response is a potential therapeutic avenue in the dysferlinopathies
    ANIMAL & CELL MODELS
  • deleted in SJL mice
  • overexpression of dysferlin in mice resulted in a striking phenotype of kyphosis, irregular gait, and reduced muscle mass and strength