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      Nesprins: from the nuclear envelope and beyond

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          Abstract

          Nuclear envelope spectrin-repeat prote ins (Nesprins), are a novel family of nuclear and cytoskeletal proteins with rapidly expanding roles as intracellular scaffolds and linkers. Originally described as proteins that localise to the nuclear envelope (NE) and establish nuclear-cytoskeletal connections, nesprins have now been found to comprise a diverse spectrum of tissue specific isoforms that localise to multiple sub-cellular compartments. Here, we describe how nesprins are necessary in maintaining cellular architecture by acting as essential scaffolds and linkers at both the NE and other sub-cellular domains. More importantly, we speculate how nesprin mutations may disrupt tissue specific nesprin scaffolds and explain the tissue specific nature of many nesprin-associated diseases, including laminopathies.

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          Most cited references49

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          Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix.

          The primary sequence of two components of the dystrophin-glycoprotein complex has been established by complementary, DNA cloning. The transmembrane 43K and extracellular 156K dystrophin-associated glycoproteins (DAGs) are encoded by a single messenger RNA and the extracellular 156K DAG binds laminin. Thus, the 156K DAG is a new laminin-binding glycoprotein which may provide a linkage between the sarcolemma and extracellular matrix. These results support the hypothesis that the dramatic reduction in the 156K DAG in Duchenne muscular dystrophy leads to a loss of a linkage between the sarcolemma and extracellular matrix and that this may render muscle fibres more susceptible to necrosis.
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            Structural requirements for the assembly of LINC complexes and their function in cellular mechanical stiffness.

            The evolutionary-conserved interactions between KASH and SUN domain-containing proteins within the perinuclear space establish physical connections, called LINC complexes, between the nucleus and the cytoskeleton. Here, we show that the KASH domains of Nesprins 1, 2 and 3 interact promiscuously with luminal domains of Sun1 and Sun2. These constructs disrupt endogenous LINC complexes as indicated by the displacement of endogenous Nesprins from the nuclear envelope. We also provide evidence that KASH domains most probably fit a pocket provided by SUN domains and that post-translational modifications are dispensable for that interaction. We demonstrate that the disruption of endogenous LINC complexes affect cellular mechanical stiffness to an extent that compares to the loss of mechanical stiffness previously reported in embryonic fibroblasts derived from mouse lacking A-type lamins, a mouse model of muscular dystrophies and cardiomyopathies. These findings support a model whereby physical connections between the nucleus and the cytoskeleton are mediated by interactions between diverse combinations of Sun proteins and Nesprins through their respective evolutionary-conserved domains. Furthermore, they emphasize, for the first time, the relevance of LINC complexes in cellular mechanical stiffness suggesting a possible involvement of their disruption in various laminopathies, a group of human diseases linked to mutations of A-type lamins.
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              Role of ANC-1 in tethering nuclei to the actin cytoskeleton.

              Mutations in anc-1 (nuclear anchorage defective) disrupt the positioning of nuclei and mitochondria in Caenorhabditis elegans. ANC-1 is shown to consist of mostly coiled regions with a nuclear envelope localization domain (called the KASH domain) and an actin-binding domain; this structure was conserved with the Drosophila protein Msp-300 and the mammalian Syne proteins. Antibodies against ANC-1 localized cytoplasmically and were enriched at the nuclear periphery in an UNC-84-dependent manner. Overexpression of the KASH domain or the actin-binding domain caused a dominant negative anchorage defect. Thus, ANC-1 may connect nuclei to the cytoskeleton by interacting with UNC-84 at the nuclear envelope and with actin in the cytoplasm.
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                Author and article information

                Journal
                Expert Rev Mol Med
                Expert Rev Mol Med
                ERM
                Expert Reviews in Molecular Medicine
                Cambridge University Press (Cambridge, UK )
                1462-3994
                2013
                : 15
                : e5
                Affiliations
                [1]James Black Centre, Cardiovascular Division, King's College London , 125 Coldharbour lane, London SE5 9NU, UK
                Author notes
                [* ]Corresponding author: C.M. Shanahan, James Black Centre, Cardiovascular Division, King's College London , 125 Coldharbour lane, London SE5 9NU, UK. E-mail: cathy.shanahan@ 123456kcl.ac.uk
                Article
                S1462399413000069 00006
                10.1017/erm.2013.6
                3733404
                23830188
                c742bbe7-f62c-4cc9-a1f5-acf085cff2bb
                © Cambridge University Press 2013

                Re-use permitted under a Creative Commons Licence – by-nc-sa.

                History
                Page count
                Figures: 6, References: 86, Pages: 17
                Categories
                Review Article

                Molecular medicine
                Molecular medicine

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