Golgi clusters and vesicles mediate mitotic inheritance independently of the endoplasmic reticulum

被引:86
作者
Jokitalo, E
Cabrera-Poch, N
Warren, G
Shima, DT
机构
[1] Imperial Canc Res Fund, Endothelial Cell Biol Lab, London WC2A 3PX, England
[2] Univ Helsinki, Inst Biotechnol, Electron Microscopy Unit, FIN-00014 Helsinki, Finland
[3] Columbia Univ Coll Phys & Surg, Dept Anat & Cell Biol, New York, NY 10032 USA
[4] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
关键词
Golgi apparatus; mitosis; endoplasmic reticulum; organelle inheritance; vesicle;
D O I
10.1083/jcb.200104073
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have examined the fate of Golgi membranes during mitotic inheritance in animal cells using four-dimensional fluorescence microscopy, serial section reconstruction of electron micrographs, and peroxidase cytochemistry to track the fate of a Golgi enzyme fused to horseradish peroxidase. All three approaches show that partitioning of Golgi membranes is mediated by Golgi clusters that persist throughout mitosis, together with shed vesicles that are often found associated with spindle microtubules. We have been unable to find evidence that Golgi membranes fuse during the later phases of mitosis with the endoplasmic reticulum (ER) as a strategy for Golgi partitioning I,Zaal, K.J., C.L. Smith, R.S. Polishchuk, N. Allan, N.B. Cole, J. Ellenberg, K. Hirschberg, J.F. Presley, T.H. Roberts, E. Siggia, et al. 1999. Cell. 99:589-601) and suggest that these results, in part, are the consequence of slow or abortive folding of GFP-Golgi chimeras in the ER. Furthermore, we show that accurate partitioning is accomplished early in mitosis, by a process of cytoplasmic redistribution of Golgi fragments and vesicles yielding a balance of Golgi membranes on either side of the metaphase plate before cell division.
引用
收藏
页码:317 / 330
页数:14
相关论文
共 53 条
  • [1] Export of cellubrevin from the endoplasmic reticulum is controlled by BAP31
    Annaert, WG
    Becker, B
    Kistner, U
    Reth, M
    Jahn, R
    [J]. JOURNAL OF CELL BIOLOGY, 1997, 139 (06) : 1397 - 1410
  • [2] GRASP65, a protein involved in the stacking of Golgi cisternae
    Barr, FA
    Puype, M
    Vandekerckhove, J
    Warren, G
    [J]. CELL, 1997, 91 (02) : 253 - 262
  • [3] BROWN WJ, 1989, METHOD CELL BIOL, V31, P553
  • [4] Inheritance of the mammalian Golgi apparatus during the cell cycle
    Cabrera-Poch, N
    Pepperkok, R
    Shima, DT
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1998, 1404 (1-2): : 139 - 151
  • [5] A specific activation of the mitogen-activated protein kinase kinase 1 (MEK1) is required for Golgi fragmentation during mitosis
    Colanzi, A
    Deerinck, TJ
    Ellisman, MH
    Malhotra, V
    [J]. JOURNAL OF CELL BIOLOGY, 2000, 149 (02) : 331 - 339
  • [6] Golgi dispersal during microtubule disruption: Regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites
    Cole, NB
    Sciaky, N
    Marotta, A
    Song, J
    LippincottSchwartz, J
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (04) : 631 - 650
  • [7] TRANSPORT INTO AND OUT OF THE GOLGI-COMPLEX STUDIED BY TRANSFECTING CELLS WITH CDNAS ENCODING HORSERADISH-PEROXIDASE
    CONNOLLY, CN
    FUTTER, CE
    GIBSON, A
    HOPKINS, CR
    CUTLER, DF
    [J]. JOURNAL OF CELL BIOLOGY, 1994, 127 (03) : 641 - 652
  • [8] The localization of human cyclins B1 and B2 determines CDK1 substrate specificity and neither enzyme requires MEK to disassemble the Golgi apparatus
    Draviam, VM
    Orrechia, S
    Lowe, M
    Pardi, R
    Pines, J
    [J]. JOURNAL OF CELL BIOLOGY, 2001, 152 (05) : 945 - 958
  • [9] Farmaki T, 1999, J CELL SCI, V112, P589
  • [10] THE GOLGI-APPARATUS (COMPLEX) (1954-1981) FROM ARTIFACT TO CENTER STAGE
    FARQUHAR, MG
    PALADE, GE
    [J]. JOURNAL OF CELL BIOLOGY, 1981, 91 (03) : S77 - S103