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FLASH GENE
Symbol SYNE1 contributors: mct/npt - updated : 23-12-2016
HGNC name spectrin repeat containing, nuclear envelope 1
HGNC id 17089
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • N-terminal calponin domains, binding filamentous actin, an actin-binding site
  • a large central spectrin-like rod domain
  • one interrupted LEM domain
  • a luminal domain binding directly to SUN proteins
  • a transmembrane anchor that tethers to the nuclear membrane
  • a short domain that resides within the lumen between the inner and outer nuclear membrane (Puckelwartz 2009)
  • C-terminal single transmembrane domain (KASH domain) spanning the outer nuclear membrane, which mediates nuclear membrane localization, and/or N-terminal paired calponin-homology domains that bind actin
  • mono polymer trimer
    HOMOLOGY
    interspecies ortholog to drosophila Msp900
    Homologene
    FAMILY
  • giant spectrin-repeat containing proteins family
  • nesprin family
  • CATEGORY motor/contractile
    SUBCELLULAR LOCALIZATION     plasma membrane
        intracellular
    intracellular,cytoplasm,organelle,Golgi
    intracellular,nucleus,nucleoplasm,nuclear bodies
    intracellular,nuclear envelope,ext
    text
  • sarcomeric Z-line of skeletal and cardiac muscle
  • at the nuclear envelope of synaptic nuclei
  • outer nuclear membrane protein that is thought to link the nucleus to the actin cytoskeleton (Zhang 2010)
  • localizes to processing bodies (PBs), where it acts as a microtubule-associated protein capable of linking mRNP complexes to microtubules
  • basic FUNCTION
  • playing an important role in muscle function
  • functioning at both the Golgi and the nuclear envelope, perhaps linking the two organelles during muscle differentiation
  • having an important function in muscle development and maintenance (Attali 2009)
  • playing a role in anchoring nuclei at the neuromuscular junction
  • multi-isomeric, spectrin-repeat proteins that bind both emerin and lamins A/C and form a network in muscle linking the nucleoskeleton to the inner nuclear membrane, the outer nuclear membrane, membraneous organelles, the sarcomere and the actin cytoskeleton
  • in combination with two SUN-domain proteins, UNC84A and UNC84B, form a linking complex that couples the nucleoskeleton to the cytoskeleton
  • participate in the LINC complex that links the cytoplasm to the nucleus (Puckelwartz 2009)
  • involved in anchoring specialized myonuclei underneath neuromuscular junctions (Attali 2009)
  • essential for normal positioning and anchorage of nuclei in skeletal muscle
  • may be forming the critical link between the nucleus and the myofibers, without which nuclear attachment to myofibers is completely abolished
  • is not a structural component of the nucleus, but is rather a coupling element that mediates interactions between F-actin and the nucleus
  • SYNE1, SYNE2 act as highly versatile tissue specific intracellular protein scaffolds
  • plays an important role in the proliferation and apoptosis of mesenchymal stem cells
  • SUN1, SUN2, SYNE1 (LINC complex) have emerged as a key regulators of actin cytoskeletal organisation
  • LINC complex exists in a mechanical feedback circuit with RHOA to regulate Vascular smooth muscle cells (VSMCs) actomyosin activity and morphology
  • mislocalization of LINC complex proteins (SUN1, SUN2, LMNA, EMD, SYNE1) is a significant characteristic of cellular senescence phenotypes and may influence complex events at the nuclear membrane, including trafficking and heterochromatin attachment
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
  • part of the LINC complex with the nesprin and SUN proteins (Puckelwartz 2009)
  • SUN2 must form a trimer to bind to SYNE1, SYNE2, and this trimerization is mediated through two predicted coiled-coil regions of the protein, CC1 and CC2, which precede the SUN domain
  • INTERACTION
    DNA
    RNA
    small molecule
    protein
  • emerin and lamin A
  • interacting with TOR1A through the KASH domain (role for torsinA in dynamic interactions between the KASH domains of nesprins and their protein partners in the lumen of the nuclear envelope, with torsinA influencing the localization of nesprins and associated cytoskeletal elements and affecting their role in nuclear and cell movement) (Nery 2008)
  • F-actin bound to SYNE1 and the actin cortical layer are considered to be involved in mechanical interaction with the nucleus
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) SCAR8 , AMCN3 , EMD4
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    constitutional germinal mutation      
    in Emery-Dreyfuss muscular dystrophy caused, in part, by uncoupling of the nucleoskeleton and cytoskeleton because of perturbed nesprin/emerin/lamin interactions)
    Susceptibility
    Variant & Polymorphism
    Candidate gene for Emery-Dreifuss muscular dystrophy (Zhang 2010)
    Marker
    Therapy target
    ANIMAL & CELL MODELS
  • mice with deletion of the C-terminus of nesprin-1 (homozygous for this mutation) exhibit lethality with approximately half dying at or near birth from respiratory failure; surviving mice display hindlimb weakness and an abnormal gait (Puckelwartz 2009)
  • young Nesprin 1–/– mice of both sexes experienced growth retardation, increased variability in body weight and decreased exercise tolerance compared with wild-type animals (Zhang 2010)