Enaptin, a giant actin-binding protein, is an element of the nuclear membrane and the actin cytoskeleton
- PMID: 15093733
- DOI: 10.1016/j.yexcr.2004.01.014
Enaptin, a giant actin-binding protein, is an element of the nuclear membrane and the actin cytoskeleton
Abstract
Enaptin belongs to a family of recently identified giant proteins that associate with the F-actin cytoskeleton as well as the nuclear membrane. It is composed of an N-terminal alpha-actinin type actin-binding domain (ABD) followed by a long coiled coil rod and a transmembrane domain at the C-terminus. The ABD binds to F-actin in vivo and in vitro and leads to bundle formation. The human Enaptin gene spreads over 515 kb and gives rise to several splicing isoforms (Nesprin-1, Myne-1, Syne-1, CPG2). The longest assembled cDNA encompasses 27,669 bp and predicts a 1014 kDa protein. Antibodies against the ABD of Enaptin localise the protein at F-actin-rich structures throughout the cell and in focal contacts as well as at the nuclear envelope. In COS7 cells, the protein is also present within the nuclear compartment. With the discovery of the actin-binding properties of Enaptin and the highly homologous Nuance, we define a family of proteins that integrate the cytoskeleton with the nucleoskeleton.
Similar articles
-
Cooperation of Cdc42 small G protein-activating and actin filament-binding activities of frabin in microspike formation.Oncogene. 2001 Jun 14;20(27):3457-63. doi: 10.1038/sj.onc.1204463. Oncogene. 2001. PMID: 11429692
-
Nesprins: intracellular scaffolds that maintain cell architecture and coordinate cell function?Expert Rev Mol Med. 2005 Jun 13;7(11):1-15. doi: 10.1017/S1462399405009294. Expert Rev Mol Med. 2005. PMID: 15953398 Review.
-
NUANCE, a giant protein connecting the nucleus and actin cytoskeleton.J Cell Sci. 2002 Aug 1;115(Pt 15):3207-22. doi: 10.1242/jcs.115.15.3207. J Cell Sci. 2002. PMID: 12118075
-
Fhos, a mammalian formin, directly binds to F-actin via a region N-terminal to the FH1 domain and forms a homotypic complex via the FH2 domain to promote actin fiber formation.J Cell Sci. 2003 Nov 15;116(Pt 22):4567-75. doi: 10.1242/jcs.00769. J Cell Sci. 2003. PMID: 14576350
-
Coronin proteins as multifunctional regulators of the cytoskeleton and membrane trafficking.Bioessays. 2005 Jun;27(6):625-32. doi: 10.1002/bies.20235. Bioessays. 2005. PMID: 15892111 Review.
Cited by
-
LINC complex alterations in DMD and EDMD/CMT fibroblasts.Eur J Cell Biol. 2012 Aug;91(8):614-28. doi: 10.1016/j.ejcb.2012.03.003. Epub 2012 May 1. Eur J Cell Biol. 2012. PMID: 22555292 Free PMC article.
-
Cell Mechanosensitivity is Enabled by the LINC Nuclear Complex.Curr Mol Biol Rep. 2016 Mar;2(1):36-47. doi: 10.1007/s40610-016-0032-8. Epub 2016 Feb 1. Curr Mol Biol Rep. 2016. PMID: 27326387 Free PMC article.
-
Nesprin 1α2 is essential for mouse postnatal viability and nuclear positioning in skeletal muscle.J Cell Biol. 2017 Jul 3;216(7):1915-1924. doi: 10.1083/jcb.201612128. Epub 2017 May 22. J Cell Biol. 2017. PMID: 28533284 Free PMC article.
-
Nesprin-1: novel regulator of striated muscle nuclear positioning and mechanotransduction.Biochem Soc Trans. 2023 Jun 28;51(3):1331-1345. doi: 10.1042/BST20221541. Biochem Soc Trans. 2023. PMID: 37171063 Free PMC article. Review.
-
Nesprin-3 regulates endothelial cell morphology, perinuclear cytoskeletal architecture, and flow-induced polarization.Mol Biol Cell. 2011 Nov;22(22):4324-34. doi: 10.1091/mbc.E11-04-0287. Epub 2011 Sep 21. Mol Biol Cell. 2011. PMID: 21937718 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases