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Vol. 10, Issue 3, 713-726, March 1999


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*Department of Biological Chemistry and The role of clathrin light chain phosphorylation in regulating
clathrin function has been examined in Saccharomyces
cerevisiae. The phosphorylation state of yeast clathrin light
chain (Clc1p) in vivo was monitored by [32P]phosphate
labeling and immunoprecipitation. Clc1p was phosphorylated in growing
cells and also hyperphosphorylated upon activation of the mating
response signal transduction pathway. Mating pheromone-stimulated hyperphosphorylation of Clc1p was dependent on the mating response signal transduction pathway MAP kinase Fus3p. Both basal and stimulated phosphorylation occurred exclusively on serines. Mutagenesis of Clc1p
was used to map major phosphorylation sites to serines 52 and 112, but
conversion of all 14 serines in Clc1p to alanines [S(all)A] was
necessary to eliminate phosphorylation. Cells expressing the S(all)A
mutant Clc1p displayed no defects in Clc1p binding to clathrin heavy
chain, clathrin trimer stability, sorting of a soluble vacuolar
protein, or receptor-mediated endocytosis of mating pheromone. However,
the trans-Golgi network membrane protein Kex2p was not
optimally localized in mutant cells. Furthermore, pheromone treatment
exacerbated the Kex2p localization defect and caused a corresponding
defect in Kex2p-mediated maturation of the
The Molecular
Biology Institute, University of California Los Angeles, Los Angeles,
California 90095-3717
-factor precursor. The
results reveal a novel requirement for clathrin during the mating
response and suggest that phosphorylation of the light chain subunit
modulates the activity of clathrin at the trans-Golgi network.
Present address: Department of Molecular
Biology and Cell Biology, University of California, Berkeley, CA
94720-3204.
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