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Vol. 9, Issue 11, 3095-3106, November 1998


and
Department of Cell Biology, Duke University Medical
Center, Durham, North Carolina 27710
We purified from Dictyostelium
lysates an 88-kDa protein that bound to a subset of small GTPases,
including racE, racC, cdc42Hs, and TC4ran, but did not bind to R-ras or
rabB. Cloning of the gene encoding this 88-kDa protein revealed that it
contained multiple armadillo-like repeats most closely
related to the mammalian GTP exchange factor smgGDS. We named
this protein darlin (Dictyostelium armadillo-like protein). Disruption of the gene encoding
darlin demonstrated that this protein is not essential for cytokinesis, pinocytosis, phagocytosis, or development. However, the ability of
darlin null cells to aggregate in response to starvation is severely
affected. When starved under liquid medium, the mutant cells were
unable to form aggregation centers and streams, possibly because of a
defect in cAMP relay signaling. This defect was not due to an inability
of the darlin mutants to activate adenylate cyclase in response to G
protein stimulation. These results suggest that the darlin protein is
involved in a signaling pathway that may modulate the chemotactic
response during early development.
Present address: Department of Biological
Chemistry, Johns Hopkins University School of Medicine, 725 North Wolfe
Street, Baltimore, MD 21205.
Present address: Department of Biology, Clark
University, 950 Main Street, Worcester, MA 01610.
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