The cytoskeleton is connected to the nuclear interior by LINC (linker of nucleoskeleton and cytoskeleton) complexes located in the nuclear envelope. These complexes consist of SUN proteins and nesprins present in the inner and outer nuclear membrane respectively. Whereas SUN proteins can bind the nuclear lamina, members of the nesprin protein family connect the nucleus to different components of the cytoskeleton. Nesprin-1 and -2 can establish a direct link with actin filaments, whereas nesprin-4 associates indirectly with microtubules through its interaction with kinesin-1. Nesprin-3 is the only family member known that can link the nuclear envelope to intermediate filaments. This indirect interaction is mediated by the binding of nesprin-3 to the cytoskeletal linker protein plectin. Furthermore, nesprin-3 can connect the nucleus to microtubules by its interactions with BPAG1 (bullous pemphigoid antigen 1) and MACF (microtubule–actin cross-linking factor). In contrast with the active roles that nesprin-1, -2 and -4 have in actin- and microtubule-dependent nuclear positioning, the role of nesprin-3 is likely to be more passive. We suggest that it helps to stabilize the anchorage of the nucleus within the cytoplasm and maintain the structural integrity and shape of the nucleus.
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December 2011
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Conference Article|
November 21 2011
Nesprin-3: a versatile connector between the nucleus and the cytoskeleton
Mirjam Ketema;
Mirjam Ketema
1Division of Cell Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands
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Arnoud Sonnenberg
Arnoud Sonnenberg
1
1Division of Cell Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands
1To whom correspondence should be addressed (email a.sonnenberg@nki.nl).
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Biochem Soc Trans (2011) 39 (6): 1719–1724.
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Received:
July 22 2011
Citation
Mirjam Ketema, Arnoud Sonnenberg; Nesprin-3: a versatile connector between the nucleus and the cytoskeleton. Biochem Soc Trans 1 December 2011; 39 (6): 1719–1724. doi: https://doi.org/10.1042/BST20110669
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