A phosphatidylinositol 3-kinase and phosphatidylinositol transfer protein act synergistically in formation of constitutive transport vesicles from the trans-Golgi network
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作者:
Jones, SM
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机构:Univ Colorado, Sch Med, Dept Cellular & Struct Biol, Denver, CO 80262 USA
Jones, SM
Alb, JG
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机构:Univ Colorado, Sch Med, Dept Cellular & Struct Biol, Denver, CO 80262 USA
Alb, JG
Phillips, SE
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机构:Univ Colorado, Sch Med, Dept Cellular & Struct Biol, Denver, CO 80262 USA
Phillips, SE
Bankaitis, VA
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机构:Univ Colorado, Sch Med, Dept Cellular & Struct Biol, Denver, CO 80262 USA
Bankaitis, VA
Howell, KE
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机构:Univ Colorado, Sch Med, Dept Cellular & Struct Biol, Denver, CO 80262 USA
Howell, KE
机构:
[1] Univ Colorado, Sch Med, Dept Cellular & Struct Biol, Denver, CO 80262 USA
[2] Univ Alabama, Dept Cell Biol, Birmingham, AL 35294 USA
Current evidence suggests that phosphatidylinositol (PI) kinases and phosphatidylinositol transfer protein (PITP) are involved in driving vesicular traffic from yeast and mammalian trans-Golgi network (TGN). We have tested the interaction between these cytosolic proteins in an assay that measures the formation of constitutive transport vesicles from the TGN in a hepatocyte cell-free system. This reaction is dependent on a novel PI 3-kinase, and we now report that, under conditions of limiting cytosol, purified PI 3-kinase and PITP functionally cooperate to drive exocytic vesicle formation. This synergy was observed with both yeast and mammalian PITPs, and it also extended to the formation of PI 3-phosphate. These collective findings indicate that the PI 3-kinase and PITP synergize to form a pool of PI 3-phosphate that is essential for formation of exocytic vesicles from the hepatocyte TGN.