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Originally published In Press as doi:10.1074/jbc.M008319200 on November 17, 2000

J. Biol. Chem., Vol. 276, Issue 7, 5235-5239, February 16, 2001
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Myosin I Phosphorylation Is Increased by Chemotactic Stimulation*

Neal R. GliksmanDagger §, Gabriela SantoyoDagger , Kristine D. NovakDagger , and Margaret A. TitusDagger ||

From the Dagger  Department of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710 and the  Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55455

Directed cell migration occurs in response to extracellular cues. Following stimulation of a cell with chemoattractant, a significant rearrangement of the actin cytoskeleton is mediated by intracellular signaling pathways and results in polarization of the cell and movement via pseudopod extension. Amoeboid myosin Is play a critical role in regulating pseudopod formation in Dictyostelium, and their activity is activated by heavy chain phosphorylation. The effect of chemotactic stimulation on the in vivo phosphorylation level of a Dictyostelium myosin I, myoB, was tested. The myoB heavy chain is phosphorylated in vivo on serine 322 (the myosin TEDS rule phosphorylation site) in chemotactically competent cells. The level of myoB phosphorylation increases following stimulation of starving cells with the chemoattractant cAMP. A 3-fold peak increase in the level of phosphorylation is observed at 60 s following stimulation, a time at which the Dictyostelium cell actively extends pseudopodia. These findings suggest that chemotactic stimulation results in increased myoB activity via heavy chain phosphorylation and contributes to the global extension of pseudopodia that occurs prior to polarization and directed motility.


* The work was supported by National Institutes of Health Grants F32-GM16090 (to N. R. G.) and GM46486 (to M. A. T.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

§ Present address: Universal Imaging Corp., 502 Brandywine Pkwy., West Chester, PA 19380.

|| To whom all correspondence should be addressed: Dept. of Genetics, Cell Biology and Development, 6-160 Jackson Hall, 321 Church St. S.E., University of Minnesota, Minneapolis, MN 55455. Tel.: 612-625-8498; Fax: 612-624-8118; E-mail: titus@lenti.med.umn.edu.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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