ArticleMolecular biology of the cell1998
The Golgi and endoplasmic reticulum remain independent during mitosis in HeLa cells.
Article in Molecular biology of the cell, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.
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Who cites it
34 citing papers in PubMed.
- Precise and economic FIB/SEM for CLEM: with 2 nm voxels through mitosis.Histochemistry and cell biology · 2018Article
- Golgi enzymes do not cycle through the endoplasmic reticulum during protein secretion or mitosis.Molecular biology of the cell · 2017Article
- GM130 Regulates Golgi-Derived Spindle Assembly by Activating TPX2 and Capturing Microtubules.Cell · 2015Article
- MEK1 inactivates Myt1 to regulate Golgi membrane fragmentation and mitotic entry in mammalian cells.The EMBO journal · 2013Article
- Human embryonic stem cells have constitutively active Bax at the Golgi and are primed to undergo rapid apoptosis.Molecular cell · 2012Article
- The Legionella pneumophila effector DrrA is sufficient to stimulate SNARE-dependent membrane fusion.Cell host & microbe · 2012Article
- Identification of a gain-of-function mutation in a Golgi P-type ATPase that enhances Mn2+ efflux and protects against toxicity.Proceedings of the National Academy of Sciences of the United States of America · 2011Article
- Mitotic inhibition of GRASP65 organelle tethering involves Polo-like kinase 1 (PLK1) phosphorylation proximate to an internal PDZ ligand.The Journal of biological chemistry · 2010Article
- Dual anchoring of the GRASP membrane tether promotes trans pairing.The Journal of biological chemistry · 2010Article
- Journeys through the Golgi--taking stock in a new era.The Journal of cell biology · 2009Review
- The alternative TrkAIII splice variant targets the centrosome and promotes genetic instability.Molecular and cellular biology · 2009Article
- Organelle tethering by a homotypic PDZ interaction underlies formation of the Golgi membrane network.The Journal of cell biology · 2009Article
- Interaction of Mint2 with TrkA is involved in regulation of nerve growth factor-induced neurite outgrowth.The Journal of biological chemistry · 2009Article
- Spatial separation of Golgi and ER during mitosis protects SREBP from unregulated activation.The EMBO journal · 2008Article
- Active ADP-ribosylation factor-1 (ARF1) is required for mitotic Golgi fragmentation.The Journal of biological chemistry · 2007Article
- Mitogen-activated protein kinase kinase 1-dependent Golgi unlinking occurs in G2 phase and promotes the G2/M cell cycle transition.Molecular biology of the cell · 2007Article
- The Golgi apparatus maintains its organization independent of the endoplasmic reticulum.Molecular biology of the cell · 2006Article
- Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells.The Journal of cell biology · 2005Article
- A cycling cis-Golgi protein mediates endosome-to-Golgi traffic.Molecular biology of the cell · 2004Article
- Cdc2 kinase-dependent disassembly of endoplasmic reticulum (ER) exit sites inhibits ER-to-Golgi vesicular transport during mitosis.Molecular biology of the cell · 2004Article
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Partitioning of the mammalian Golgi apparatus during cell division involves disassembly at M-phase. Despite the importance of the disassembly/reassembly pathway in Golgi biogenesis, it remains unclear whether mitotic Golgi breakdown in vivo proceeds by direct vesiculation or involves fusion with the endoplasmic reticulum (ER). To test whether mitotic Golgi is fused with the ER, we compared the distribution of ER and Golgi proteins in interphase and mitotic HeLa cells by immunofluorescence microscopy, velocity gradient fractionation, and density gradient fractionation. While mitotic ER appeared to be a fine reticulum excluded from the region containing the spindle-pole body, mitotic Golgi appeared to be dispersed small vesicles that penetrated the area containing spindle microtubules. After cell disruption, M-phase Golgi was recovered in two size classes. The major breakdown product, accounting for at least 75% of the Golgi, was a population of 60-nm vesicles that were completely separated from the ER using velocity gradient separation. The minor breakdown product was a larger, more heterogenously sized, membrane population. Double-label fluorescence analysis of these membranes indicated that this portion of mitotic Golgi also lacked detectable ER marker proteins. Therefore we conclude that the ER and Golgi remain distinct at M-phase in HeLa cells. To test whether the 60-nm vesicles might form from the ER at M-phase as the result of a two-step vesiculation pathway involving ER-Golgi fusion followed by Golgi vesicle budding, mitotic cells were generated with fused ER and Golgi by brefeldin A treatment. Upon brefeldin A removal, Golgi vesicles did not emerge from the ER. In contrast, the Golgi readily reformed from similarly treated interphase cells. We conclude that Golgi-derived vesicles remain distinct from the ER in mitotic HeLa cells, and that mitotic cells lack the capacity of interphase cells for Golgi reemergence from the ER. These experiments suggest that mitotic Golgi breakdown proceeds by direct vesiculation independent of the ER.
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