Cytosol dependent membrane fusion in ER, nuclear envelope and nuclear pore assembly

References

• Lohka MJ, Masui Y. Formation in vitro of sperm pronuclei and mitotic chromosomes induced by amphibian ooplasmic components. Science 1983; 220:719 - 721
   PubMed Web of Science ®Google Scholar
• Sheehan MA, Mills AD, Sleeman AM, Laskey RA, Blow JJ. Steps in the assembly of replication-competent nuclei in a cell-free system from Xenopus eggs. J Cell Biol 1988; 106:1 - 12
   PubMed Web of Science ®Google Scholar
• Rafikova ER, Melikov K, Ramos C, Dye L, Chernomordik LV. Transmembrane protein-free membranes fuse into xenopus nuclear envelope and promote assembly of functional pores. J Biol Chem 2009; 284:29847 - 29859
   PubMed Web of Science ®Google Scholar
• Hetzer MW, Wente SR. Border control at the nucleus: biogenesis and organization of the nuclear membrane and pore complexes. Dev Cell 2009; 17:606 - 616
   PubMed Web of Science ®Google Scholar
• Anderson DJ, Hetzer MW. Nuclear envelope formation by chromatin-mediated reorganization of the endoplasmic reticulum. Nat Cell Biol 2007; 9:1160 - 1166
   PubMed Web of Science ®Google Scholar
• Larijani B, Poccia DL. Nuclear envelope formation: mind the gaps. Annu Rev Biophys 2009; 38:107 - 124
   PubMed Web of Science ®Google Scholar
• Jahn R, Scheller RH. SNAREs—engines for membrane fusion. Nat Rev Mol Cell Biol 2006; 7:631 - 643
   PubMed Web of Science ®Google Scholar
• Lee C, Chen LB. Dynamic behavior of endoplasmic reticulum in living cells. Cell 1988; 54:37 - 46
   PubMed Web of Science ®Google Scholar
• Voeltz GK, Prinz WA, Shibata Y, Rist JM, Rapoport TA. A class of membrane proteins shaping the tubular endoplasmic reticulum. Cell 2006; 124:573 - 586
   PubMed Web of Science ®Google Scholar
• Hu J, Shibata Y, Voss C, Shemesh T, Li Z, Coughlin M, et al. Membrane proteins of the endoplasmic reticulum induce high-curvature tubules. Science 2008; 319:1247 - 1250
   PubMed Web of Science ®Google Scholar
• Hu J, Shibata Y, Zhu PP, Voss C, Rismanchi N, Prinz WA, et al. A class of dynamin-like GTPases involved in the generation of the tubular ER network. Cell 2009; 138:549 - 561
   PubMed Web of Science ®Google Scholar
• Orso G, Pendin D, Liu S, Tosetto J, Moss TJ, Faust JE, et al. Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin. Nature 2009; 460:978 - 983
   Google Scholar
• Puhka M, Vihinen H, Joensuu M, Jokitalo E. Endoplasmic reticulum remains continuous and undergoes sheet-to-tubule transformation during cell division in mammalian cells. J Cell Biol 2007; 179:895 - 909
   PubMed Web of Science ®Google Scholar
• Lu L, Ladinsky MS, Kirchhausen T. Cisternal organization of the endoplasmic reticulum during mitosis. Mol Biol Cell 2009; 20:3471 - 3480
   PubMed Web of Science ®Google Scholar
• Poteryaev D, Squirrell JM, Campbell JM, White JG, Spang A. Involvement of the actin cytoskeleton and homotypic membrane fusion in ER dynamics in Caenorhabditis elegans. Mol Biol Cell 2005; 16:2139 - 2153
   PubMed Web of Science ®Google Scholar
• Ishihara N, Eura Y, Mihara K. Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity. J Cell Sci 2004; 117:6535 - 6546
   PubMed Web of Science ®Google Scholar
• Podbilewicz B, Leikina E, Sapir A, Valansi C, Suissa M, Shemer G, et al. The C. elegans developmental fusogen EFF-1 mediates homotypic fusion in heterologous cells and in vivo. Dev Cell 2006; 11:471 - 481
   PubMed Web of Science ®Google Scholar
• Ramos C, Rafikova ER, Melikov K, Chernomordik LV. Transmembrane proteins are not required for early stages of nuclear envelope assembly. Biochem J 2006; 400:393 - 400
   PubMed Web of Science ®Google Scholar
• Chernomordik LV, Kozlov MM. Protein-lipid interplay in fusion and fission of biological membranes. Annu Rev Biochem 2003; 72:175 - 207
   PubMed Web of Science ®Google Scholar
• Wilson KL, Newport J. A trypsin-sensitive receptor on membrane vesicles is required for nuclear envelope formation in vitro. J Cell Biol 1988; 107:57 - 68
   PubMed Web of Science ®Google Scholar
• Baur T, Ramadan K, Schlundt A, Kartenbeck J, Meyer HH. NSF- and SNARE-mediated membrane fusion is required for nuclear envelope formation and completion of nuclear pore complex assembly in Xenopus laevis egg extracts. J Cell Sci 2007; 120:2895 - 2903
   PubMed Web of Science ®Google Scholar
• Vogel K, Cabaniols JP, Roche PA. Targeting of SNAP-25 to membranes is mediated by its association with the target SNARE syntaxin. J Biol Chem 2000; 275:2959 - 2965
   PubMed Web of Science ®Google Scholar
• He Y, Linder ME. Differential palmitoylation of the endosomal SNAREs syntaxin 7 and syntaxin 8. J Lipid Res 2009; 50:398 - 404
   PubMed Web of Science ®Google Scholar
• Langosch D, Hofmann M, Ungermann C. The role of transmembrane domains in membrane fusion. Cell Mol Life Sci 2007; 64:850 - 864
   PubMed Web of Science ®Google Scholar
• Leikina E, LeDuc DL, Macosko JC, Epand R, Shin YK, Chernomordik LV. The 1-127 HA2 construct of influenza virus hemagglutinin induces cell-cell hemifusion. Biochemistry 2001; 40:8378 - 8386
   PubMed Web of Science ®Google Scholar
• Martens S, Kozlov MM, McMahon HT. How synaptotagmin promotes membrane fusion. Science 2007; 316:1205 - 1208
   PubMed Web of Science ®Google Scholar
• Melloy P, Shen S, White E, Rose MD. Distinct roles for key karyogamy proteins during yeast nuclear fusion. Mol Biol Cell 2009; 20:3773 - 3782
   PubMed Web of Science ®Google Scholar
• Shen S, Tobery CE, Rose MD. Prm3p is a pheromone-induced peripheral nuclear envelope protein required for yeast nuclear fusion. Mol Biol Cell 2009; 20:2438 - 2450
   PubMed Web of Science ®Google Scholar
• Nakatogawa H, Ichimura Y, Ohsumi Y. Atg8, a ubiquitin-like protein required for autophagosome formation, mediates membrane tethering and hemifusion. Cell 2007; 130:165 - 178
   PubMed Web of Science ®Google Scholar
• McNeil AK, Rescher U, Gerke V, McNeil PL. Requirement for annexin A1 in plasma membrane repair. J Biol Chem 2006; 281:35202 - 35207
   PubMed Web of Science ®Google Scholar
• Tomas A, Moss SE. Calcium- and cell cycle-dependent association of annexin 11 with the nuclear envelope. J Biol Chem 2003; 278:20210 - 20216
   PubMed Web of Science ®Google Scholar
• Skrahina T, Piljic A, Schultz C. Heterogeneity and timing of translocation and membrane-mediated assembly of different annexins. Exp Cell Res 2008; 314:1039 - 1047
   PubMed Web of Science ®Google Scholar
• Chernomordik LV, Kozlov MM. Mechanics of membrane fusion. Nat Struct Mol Biol 2008; 15:675 - 683
   PubMed Web of Science ®Google Scholar
• McMahon HT, Kozlov MM, Martens S. Membrane curvature in synaptic vesicle fusion and beyond. Cell 2010; 140:601 - 605
   PubMed Web of Science ®Google Scholar
• Zimmerberg J, Kozlov MM. How proteins produce cellular membrane curvature. Nat Rev Mol Cell Biol 2006; 7:9 - 19
   PubMed Web of Science ®Google Scholar
• Davis LI, Blobel G. Nuclear pore complex contains a family of glycoproteins that includes p62: glycosylation through a previously unidentified cellular pathway. Proc Natl Acad Sci USA 1987; 84:7552 - 7556
   PubMed Web of Science ®Google Scholar
• Verschure PJ, van der Kraan I, Manders EM, Hoogstraten D, Houtsmuller AB, van Driel R. Condensed chromatin domains in the mammalian nucleus are accessible to large macromolecules. EMBO Rep 2003; 4:861 - 866
   PubMed Web of Science ®Google Scholar
• Rasala BA, Ramos C, Harel A, Forbes DJ. Capture of AT-rich chromatin by ELYS recruits POM121 and NDC1 to initiate nuclear pore assembly. Mol Biol Cell 2008; 19:3982 - 3996
   PubMed Web of Science ®Google Scholar
• Rotem A, Gruber R, Shorer H, Shaulov L, Klein E, Harel A. Importin beta regulates the seeding of chromatin with initiation sites for nuclear pore assembly. Mol Biol Cell 2009; 20:4031 - 4042
   PubMed Web of Science ®Google Scholar
• Maul GG, Price JW, Lieberman MW. Formation and distribution of nuclear pore complexes in interphase. J Cell Biol 1971; 51:405 - 418
   PubMed Web of Science ®Google Scholar
• Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, et al. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA 2004; 101:8963 - 8968
   PubMed Web of Science ®Google Scholar