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Vol. 13, Issue 7, 2193-2206, July 2002

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and
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*Department of Cell Biology, University of Alabama at Birmingham,
Birmingham, Alabama 35294-0005; Yeast phosphatidylinositol transfer protein (Sec14p)
coordinates lipid metabolism with protein-trafficking events. This
essential Sec14p requirement for Golgi function is bypassed by
mutations in any one of seven genes that control phosphatidylcholine or phosphoinositide metabolism. In addition to these "bypass Sec14p" mutations, Sec14p-independent Golgi function requires phospholipase D
activity. The identities of lipids that mediate Sec14p-dependent Golgi
function, and the identity of the proteins that respond to
Sec14p-mediated regulation of lipid metabolism, remain elusive. We now
report genetic evidence to suggest that two ADP ribosylation factor-GTPase-activating proteins (ARFGAPs), Gcs1p and Age2p, may
represent these lipid-responsive elements, and that Gcs1p/Age2p act
downstream of Sec14p and phospholipase D in both
Sec14p-dependent and Sec14p-independent pathways for yeast Golgi
function. In support, biochemical data indicate that Gcs1p and Age2p
ARFGAP activities are both modulated by lipids implicated in regulation
of Sec14p pathway function. These results suggest ARFGAPs are
stimulatory factors required for regulation of Golgi function by the
Sec14p pathway, and that Sec14p-mediated regulation of lipid metabolism interfaces with the activity of proteins involved in control of the ARF cycle.
Department of Cell and
Developmental Biology, Lineberger Comprehensive Cancer Center,
University of North Carolina at Chapel Hill, Chapel Hill, North
Carolina 27599-7090;
Departments of Microbiology and
Immunology, and §Biochemistry and Molecular Biology,
Dalhousie University, Halifax, Nova Scotia, Canada B3H 4H7; and
Laboratory of Cellular Oncology, Division of Basic
Sciences, National Cancer Institute, Bethesda, Maryland 20892
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