[HTML][HTML] The vesicle docking protein p115 binds GM130, a cis-Golgi matrix protein, in a mitotically regulated manner

N Nakamura, M Lowe, TP Levine, C Rabouille… - Cell, 1997 - cell.com
N Nakamura, M Lowe, TP Levine, C Rabouille, G Warren
Cell, 1997cell.com
The docking of transport vesicles with their target membrane is thought to be mediated by
p115. We show here that GM130, a cis-Golgi matrix protein, interacts specifically with p115
and so could provide a membrane docking site. Deletion analysis showed that the N-
terminus binds to p115, whereas the C-terminus binds to Golgi membranes. Mitotic
phosphorylation of GM130 or a peptide derived from the N-terminus prevented binding to
p115. The peptide also inhibited the NSF-but not the p97-dependent reassembly of Golgi …
Abstract
The docking of transport vesicles with their target membrane is thought to be mediated by p115. We show here that GM130, a cis-Golgi matrix protein, interacts specifically with p115 and so could provide a membrane docking site. Deletion analysis showed that the N-terminus binds to p115, whereas the C-terminus binds to Golgi membranes. Mitotic phosphorylation of GM130 or a peptide derived from the N-terminus prevented binding to p115. The peptide also inhibited the NSF- but not the p97-dependent reassembly of Golgi cisternae from mitotic fragments, unless it was mitotically phosphorylated. Together, these data provide a molecular explanation for the COPI-mediated fragmentation of the Golgi apparatus at the onset of mitosis.
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