Nuclear membrane disassembly and rupture

被引:20
作者
Cotter, Laura
Allen, Terence D.
Kiseleva, Elena
Goldberg, Martin W.
机构
[1] Christie Hosp, Paterson Inst Canc Res, Manchester M20 4BX, Lancs, England
[2] Russian Acad Sci, Inst Cytol & Genet, Lab Morphol & Funct Cell Struct, Novosibirsk 630090, Russia
[3] Univ Durham, Sch Biol & Biomed Sci, Durham DH1 3LE, England
基金
英国惠康基金;
关键词
nuclear envelope; pore complex; disassembly;
D O I
10.1016/j.jmb.2007.03.051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nuclear envelope consists of two membranes traversed by nuclear pore complexes. The outer membrane is continuous with the endoplasmic reticulum. At mitosis nuclear pore complexes are dismantled and membranes disperse. The mechanism of dispersal is controversial: one view is that membranes feed into the endoplasmic reticulum, another is that they vesiculate. Using Xenopus egg extracts, nuclei have been assembled and then induced to breakdown by addition of metaphase extract. Field emission scanning electron microscopy was used to study disassembly. Strikingly, endoplasmic reticulum-like membrane tubules form from the nuclear surface after the addition of metaphase extracts, but vesicles were also observed. Microtubule inhibitors slowed but did not prevent membrane removal, whereas Brefeldin A, which inhibits vesicle formation, stops membrane disassembly, suggesting that vesiculation is necessary. Structures that looked like coated buds were observed and buds were labelled for beta-COR We show that nuclear pore complexes are dismantled and the pore closed prior to membrane rupturing, suggesting that rupturing is an active process rather than a result of enlargement of nuclear pores. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:683 / 695
页数:13
相关论文
共 61 条
[1]   ARCHITECTURE OF THE XENOPUS NUCLEAR-PORE COMPLEX REVEALED BY 3-DIMENSIONAL CRYOELECTRON MICROSCOPY [J].
AKEY, CW ;
RADERMACHER, M .
JOURNAL OF CELL BIOLOGY, 1993, 122 (01) :1-19
[2]   INTERACTIONS AND STRUCTURE OF THE NUCLEAR-PORE COMPLEX REVEALED BY CRYO-ELECTRON MICROSCOPY [J].
AKEY, CW .
JOURNAL OF CELL BIOLOGY, 1989, 109 (03) :955-970
[3]   CELL-CYCLE CONTROL OF MICROTUBULE-BASED MEMBRANE-TRANSPORT AND TUBULE FORMATION INVITRO [J].
ALLAN, VJ ;
VALE, RD .
JOURNAL OF CELL BIOLOGY, 1991, 113 (02) :347-359
[4]   ASSAY OF MEMBRANE MOTILITY IN INTERPHASE AND METAPHASE XENOPUS EXTRACTS [J].
ALLAN, VJ .
METHODS IN CELL BIOLOGY, VOL 39: MOTILITY ASSAYS FOR MOTOR PROTEINS, 1993, 39 :203-226
[5]   Nuclear envelope breakdown proceeds by microtubule-induced tearing of the lamina [J].
Beaudouin, J ;
Gerlich, D ;
Daigle, N ;
Eils, R ;
Ellenberg, J .
CELL, 2002, 108 (01) :83-96
[6]   Nuclear pore complex structure and dynamics revealed by cryoelectron tomography [J].
Beck, M ;
Förster, F ;
Ecke, M ;
Plitzko, JM ;
Melchior, F ;
Gerisch, G ;
Baumeister, W ;
Medalia, O .
SCIENCE, 2004, 306 (5700) :1387-1390
[7]   Cruising along microtubule highways: How membranes move through the secretory pathway [J].
Bloom, GS ;
Goldstein, LSB .
JOURNAL OF CELL BIOLOGY, 1998, 140 (06) :1277-1280
[8]   GTP HYDROLYSIS IS REQUIRED FOR VESICLE FUSION DURING NUCLEAR-ENVELOPE ASSEMBLY INVITRO [J].
BOMAN, AL ;
DELANNOY, MR ;
WILSON, KL .
JOURNAL OF CELL BIOLOGY, 1992, 116 (02) :281-294
[9]   The mechanisms of vesicle budding and fusion [J].
Bonifacino, JS ;
Glick, BS .
CELL, 2004, 116 (02) :153-166
[10]   Laminopathies [J].
Broers, JLV ;
Hutchison, CJ ;
Ramaekers, FCS .
JOURNAL OF PATHOLOGY, 2004, 204 (04) :478-488