共 62 条
Syntaxin 5 is a common component of the NSF- and p97-mediated reassembly pathways of Golgi cisternae from mitotic Golgi fragments in vitro
被引:220
作者:

Rabouille, C
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机构: Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England

Kondo, H
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机构: Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England

Newman, R
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机构: Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England

Hui, N
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机构: Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England

Freemont, P
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机构: Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England

Warren, G
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机构: Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England
机构:
[1] Imperial Canc Res Fund, Cell Biol Lab, London WC2A 3PX, England
[2] Imperial Canc Res Fund, Mol Struct & Funct Lab, London WC2A 3PX, England
来源:
关键词:
D O I:
10.1016/S0092-8674(00)81128-9
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:
A cell-free system that mimics the reassembly of Golgi stacks at the end of mitosis requires two ATPases, NSF and p97, to rebuild Golgi cisternae. Morphological studies now show that alpha-SNAP, a component of the NSF pathway, can inhibit the p97 pathway, whereas p47, a component of the p97 pathway, can inhibit the NSF pathway. Anti-syntaxin 5 antibodies and a soluble, recombinant syntaxin 5 inhibited both pathways, suggesting that this t-SNARE is a common component. Biochemical studies confirmed this, showing that p47 binds directly to syntaxin 5 and competes for binding with alpha-SNAP. p47 also mediates the binding of p97 to syntaxin 5 and so plays an analogous role to alpha-SNAP, which mediates the binding of NSF.
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页码:603 / 610
页数:8
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