NSF- and SNARE-mediated membrane fusion is required for nuclear envelope formation and completion of nuclear pore complex assembly in Xenopus laevis egg extracts

被引:41
作者
Baur, Tina
Ramadan, Kristijan
Schlundt, Andreas
Kartenbeck, Juergen
Meyer, Hemmo H. [1 ]
机构
[1] ETH, Inst Biochem, CH-8093 Zurich, Switzerland
[2] ETH, Inst Appl Phys, CH-8093 Zurich, Switzerland
关键词
membrane fusion; nuclear envelope; nuclear pore; NSF; SNAP;
D O I
10.1242/jcs.010181
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Despite the progress in understanding nuclear envelope (NE) reformation after mitosis, it has remained unclear what drives the required membrane fusion and how exactly this is coordinated with nuclear pore complex (NPC) assembly. Here, we show that, like other intracellular fusion reactions, NE fusion in Xenopus laevis egg extracts is mediated by SNARE proteins that require activation by NSF. Antibodies against Xenopus NSF, depletion of NSF or the dominant-negative NSFE329Q variant specifically inhibited NE formation. Staging experiments further revealed that NSF was required until sealing of the envelope was completed. Moreover, excess exogenous alpha-SNAP that blocks SNARE function prevented membrane fusion and caused accumulation of non-flattened vesicles on the chromatin surface. Under these conditions, the nucleoporins Nup107 and gp210 were fully recruited, whereas assembly of FxFG-repeat-containing nucleoporins was blocked. Together, we define NSF- and SNARE-mediated membrane fusion events as essential steps during NE formation downstream of Nup107 recruitment, and upstream of membrane flattening and completion of NPC assembly.
引用
收藏
页码:2895 / 2903
页数:9
相关论文
共 39 条
[1]   The integral membrane nucleoporin pom121 functionally links nuclear pore complex assembly and nuclear envelope formation [J].
Antonin, W ;
Franz, C ;
Haselmann, U ;
Antony, C ;
Mattaj, IW .
MOLECULAR CELL, 2005, 17 (01) :83-92
[2]   Stimulation of NSF ATPase activity by alpha-SNAP is required for SNARE complex disassembly and exocytosis [J].
Barnard, RJO ;
Morgan, A ;
Burgoyne, RD .
JOURNAL OF CELL BIOLOGY, 1997, 139 (04) :875-883
[3]   An evolutionarily conserved NPC subcomplex, which redistributes in part to kinetochores in mammalian cells [J].
Belgareh, N ;
Rabut, G ;
Baï, SW ;
van Overbeek, M ;
Beaudouin, J ;
Daigle, N ;
Zatsepina, OV ;
Pasteau, F ;
Labas, V ;
Fromont-Racine, M ;
Ellenberg, J ;
Doye, V .
JOURNAL OF CELL BIOLOGY, 2001, 154 (06) :1147-1160
[4]   PURIFICATION OF AN N-ETHYLMALEIMIDE-SENSITIVE PROTEIN CATALYZING VESICULAR TRANSPORT [J].
BLOCK, MR ;
GLICK, BS ;
WILCOX, CA ;
WIELAND, FT ;
ROTHMAN, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :7852-7856
[5]  
Bodoor K, 1999, J CELL SCI, V112, P2253
[6]   Depletion of a single nucleoporin, Nup107, prevents the assembly of a subset of nucleoporins into the nuclear pore complex [J].
Boehmer, T ;
Enninga, J ;
Dales, S ;
Blobel, G ;
Zhong, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :981-985
[7]   Remodelling the walls of the nucleus [J].
Burke, B ;
Ellenberg, J .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (07) :487-497
[8]   Nuclear pores form de novo from both sides of the nuclear envelope [J].
D'Angelo, MA ;
Anderson, DJ ;
Richard, E ;
Hetzer, MW .
SCIENCE, 2006, 312 (5772) :440-443
[9]   In vitro formation of the endoplasmic reticulum occurs independently of microtubules by a controlled fusion reaction [J].
Dreier, L ;
Rapoport, TA .
JOURNAL OF CELL BIOLOGY, 2000, 148 (05) :883-898
[10]   Interference with the cytoplasmic tail of gp210 disrupts "close apposition" of nuclear membranes and blocks nuclear pore dilation [J].
Drummond, SP ;
Wilson, KL .
JOURNAL OF CELL BIOLOGY, 2002, 158 (01) :53-62