Fragmentation and dispersal of the pericentriolar Golgi complex is required for entry into mitosis in mammalian cells
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Sütterlin, C
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机构:Univ Calif San Diego, Div Biol, Dept Cell & Dev Biol, La Jolla, CA 92093 USA
Sütterlin, C
Hsu, P
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机构:Univ Calif San Diego, Div Biol, Dept Cell & Dev Biol, La Jolla, CA 92093 USA
Hsu, P
Mallabiabarrena, A
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机构:Univ Calif San Diego, Div Biol, Dept Cell & Dev Biol, La Jolla, CA 92093 USA
Mallabiabarrena, A
Malhotra, V
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Univ Calif San Diego, Div Biol, Dept Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol, Dept Cell & Dev Biol, La Jolla, CA 92093 USA
Malhotra, V
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[1] Univ Calif San Diego, Div Biol, Dept Cell & Dev Biol, La Jolla, CA 92093 USA
The pericentriolar Golgi stacks are fragmented and found dispersed in mitotic mammalian cells. Addition of an antibody to the Golgi-associated protein GRASP65 inhibited Golgi fragmentation by mitotic cytosol in permeabilized cells. Microinjecting this antibody or the C-terminal fragment of GRASP65, which contains the antibody binding site, into normal rat kidney cells prevented entry into mitosis. Under these conditions the cells had completed S phase but were not in the prophase stage of mitosis. Fragmentation of the Golgi apparatus by nocodazole or Brefeldin A treatment prior to or post microinjection of the anti-GRASP65 antibody alleviated the block in mitotic entry. Based on our findings, we suggest that the pericentriolar Golgi organization is a sensor for controlling entry into mitosis in mammalian cells.