Disruption of the presynaptically enriched polyphosphoinositide phosphatase
synaptojanin 1 leads to an increase of clathrin-coated intermediates and o
f polymerized actin at endocytic zones of nerve terminals. These changes co
rrelate with elevated levels of PI(4,5)P-2 in neurons. We report that phosp
hatidylinositol phosphate kinase type I gamma (PIPKI gamma), a major brain
PI(4)P 5-kinase, is concentrated at synapses. Synaptojanin 1 and PIPKI gamm
a antagonize each other in the recruitment of clathrin coats to lipid membr
anes. Like synaptojanin 1 and other proteins involved in endocytosis, PIPKI
gamma undergoes stimulation-dependent dephosphorylation. These results imp
licate PIPKI gamma in the synthesis of a PI(4,5)P-2 pool that acts as a pos
itive regulator of clathrin coat recruitment and actin function at the syna
pse.