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Cells migrating directionally toward a chemoattractant sourcedisplay a highly polarized cytoskeletal organization, with F-actinlocalized predominantly at the anterior and myosin II at thelateral and posterior regions. Dictyostelium discoideum hasproven a useful system for elucidating signaling pathways thatregulate this chemotactic response. During development, extracellularadenosine 3', 5' monophosphate (cAMP) functions as a primarysignal to activate cell surface cAMP receptors (cARs). Thesereceptors transduce different signals depending on whether ornot they are coupled to heterotrimeric guanine nucleotidebindingproteins (G proteins) (see the STKE Connections Maps). MultipleG proteinstimulated pathways interact to establish polarityin chemotaxing D. discoideum cells by localizing F-actin attheir leading edge and by regulating the phosphorylation stateand assembly of myosin II. Many of the molecular interactionsdescribed are fundamental to the regulation of chemotaxis inother eukaryotic cells.
1 Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892, USA. 2 Laboratory of Cellular and Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
* To whom correspondence should be addressed. E-mail: parentc{at}helix.nih.gov
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