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Vol. 13, Issue 10, 3646-3661, October 2002


and
*The Henry Wellcome Laboratory for Cell Biology, Institute of
Biomedical and Life Sciences, University of Glasgow, Glasgow G12 8QQ,
Scotland, United Kingdom; and The importance of coupling the process of endocytosis to factors
regulating actin dynamics has been clearly demonstrated in yeast, and
many proteins involved in these mechanisms have been identified and
characterized. Here we demonstrate the importance of two additional
cortical components, Ysc84p and Lsb5p, which together are essential for
the organization of the actin cytoskeleton and for fluid phase
endocytosis. Both Ysc84p and Lsb5p were identified through two-hybrid
screens with different domains of the adaptor protein Sla1p. Ysc84p
colocalizes with cortical actin and requires the presence of an intact
actin cytoskeleton for its cortical localization. Ycl034w/Lsb5p
localizes to the cell cortex but does not colocalize with actin. The
Lsb5 protein contains putative VHS and GAT domains as well as an NPF
motif, which are all domains characteristic of proteins involved in
membrane trafficking. Deletion of either gene alone does not confer any
dramatic phenotype on cells. However, deletion of both genes is lethal
at elevated temperatures. Furthermore, at all temperatures this double
mutant has depolarized actin and an almost undetectable level of fluid
phase endocytosis. Our data demonstrate that Ysc84p and Lsb5p are
important components of complexes involved in overlapping pathways
coupling endocytosis with the actin cytoskeleton in yeast.
Wellcome Trust Biocentre,
Division of Molecular Cell Biology, School of Life Sciences, University
of Dundee, Dundee DD1 5EH, Scotland
Both authors contributed equally to this work.
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