共 36 条
Type I phosphatidylinositol 4-phosphate 5-kinase directly interacts with ADP-ribosylation factor 1 and is responsible for phosphatidylinositol 4,5-bisphosphate synthesis in the Golgi compartment
被引:140
作者:

Jones, DH
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机构: UCL, Dept Physiol, London WC1E 6JJ, England

Morris, JB
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机构: UCL, Dept Physiol, London WC1E 6JJ, England

Morgen, CP
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机构: UCL, Dept Physiol, London WC1E 6JJ, England

Kondo, H
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机构: UCL, Dept Physiol, London WC1E 6JJ, England

Irvine, RF
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h-index: 0
机构: UCL, Dept Physiol, London WC1E 6JJ, England

Cockcroft, S
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h-index: 0
机构:
UCL, Dept Physiol, London WC1E 6JJ, England UCL, Dept Physiol, London WC1E 6JJ, England
机构:
[1] UCL, Dept Physiol, London WC1E 6JJ, England
[2] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
[3] Tohoku Univ, Sch Med, Dept Anat, Sendai, Miyagi 980, Japan
关键词:
D O I:
10.1074/jbc.C901019199
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:
Phosphatidylinositol (PtdIns) 4,5-bisphosphate is involved in many aspects of membrane traffic, but the regulation of its synthesis is only partially understood. Golgi membranes contain PI 4-kinase activity and a pool of phosphatidylinositol phosphate (PIP), which is further increased by ADP-ribosylation factor 1 (ARF1). COS7 cells were transfected with alpha and beta forms of PI 4-kinase, and only membranes from COS7 cells transfected with PI 4-kinase beta increased their content of PIP when incubated with ARF1. PtdIns(4,5)P(2) content in Golgi membranes was nonexistent but could be increased to a small extent upon adding either cytosol or Type I or Type II PIP kinases. However, when ARF1 was present, Ptdins(4,5)P(2) levels increased dramatically when membranes were incubated in the presence of cytosol or Type I, but not Type II, PIP kinase. To examine whether ARF1 could directly activate Type I PIP 5-kinase, we used an in vitro assay consisting of phosphatidycholine-containing liposomes, ARF1, and PIP 5-kinase, ARF1 increased Type I PIP 5-kinase activity in a guanine nucleotide-dependent manner, identifying this enzyme as a direct effector for ARF1.
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页码:13962 / 13966
页数:5
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