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Vol. 12, Issue 1, 201-219, January 2001
Sinsheimer Labs, Department of Molecular, Cellular, and
Developmental Biology, University of California, Santa Cruz, Santa
Cruz, California 95064
We have used affinity chromatography to identify proteins that
interact with Nap1, a protein previously shown to play a role in
mitosis. Our studies demonstrate that a highly conserved protein called
Sda1 binds to Nap1 both in vitro and in vivo. Loss of Sda1 function
causes cells to arrest uniformly as unbudded cells that do not increase
significantly in size. Cells arrested by loss of Sda1 function have a
1N DNA content, fail to produce the G1 cyclin Cln2, and remain
responsive to mating pheromone, indicating that they arrest in G1
before Start. Expression of CLN2 from a heterologous
promoter in temperature-sensitive sda1 cells induces bud
emergence and polarization of the actin cytoskeleton, but does not
induce cell division, indicating that the sda1 cell
cycle arrest phenotype is not due simply to a failure to produce the G1
cyclins. The Sda1 protein is absent from cells arrested in G0 and is
expressed before Start when cells reenter the cell cycle, further
suggesting that Sda1 functions before Start. Taken together, these
findings reveal that Sda1 plays a critical role in G1 events. In
addition, these findings suggest that Nap1 is likely to function during
G1. Consistent with this, we have found that Nap1 is required for
viability in cells lacking the redundant G1 cyclins Cln1 and Cln2. In
contrast to a previous study, we have found no evidence that Sda1 is
required for the assembly or function of the actin cytoskeleton.
Further characterization of Sda1 is likely to provide important clues
to the poorly understood mechanisms that control passage through G1.
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