Cell migration occurs through the protrusion of the actin-enriched lamella. Here, we investigated the effects of RNAi depletion of ∼90 proteins implicated in actin function on lamella formation in Drosophila S2 cells. Similar to in vitro reconstitution studies of actin-based Listeria movement, we find that lamellae formation requires a relatively small set of proteins that participate in actin nucleation (Arp2/3 and SCAR), barbed end capping (capping protein), filament depolymerization (cofilin and Aip1), and actin monomer binding (profilin and cyclase-associated protein). Lamellae are initiated by parallel and partially redundant signaling pathways involving Rac GTPases and the adaptor protein Nck, which stimulate SCAR, an Arp2/3 activator. We also show that RNAi of three proteins (kette, Abi, and Sra-1) known to copurify with and inhibit SCAR in vitro leads to SCAR degradation, revealing a novel function of this protein complex in SCAR stability. Our results have identified an essential set of proteins involved in actin dynamics during lamella formation in Drosophila S2 cells.
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15 September 2003
Article|
September 15 2003
Molecular requirements for actin-based lamella formation in Drosophila S2 cells
Stephen L. Rogers,
Stephen L. Rogers
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
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Ursula Wiedemann,
Ursula Wiedemann
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
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Nico Stuurman,
Nico Stuurman
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
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Ronald D. Vale
Ronald D. Vale
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
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Stephen L. Rogers
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
Ursula Wiedemann
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
Nico Stuurman
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
Ronald D. Vale
Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
Address correspondence to Ron Vale, Department of Cellular and Molecular Pharmacology, University of California, San Francisco, N312 Genentech Hall, 600 16th Street, San Francisco, CA 94107. Tel.: (415) 476-6380. Fax: (415) 476-5233. email: [email protected]
The online version of this article includes supplemental material.
Abbreviations used in this paper: CAP, cyclase-associated protein; con A, concanavalin A; VASP, vasodilator-stimulated phosphoprotein.
Received:
March 04 2003
Accepted:
July 28 2003
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2003
J Cell Biol (2003) 162 (6): 1079–1088.
Article history
Received:
March 04 2003
Accepted:
July 28 2003
Citation
Stephen L. Rogers, Ursula Wiedemann, Nico Stuurman, Ronald D. Vale; Molecular requirements for actin-based lamella formation in Drosophila S2 cells . J Cell Biol 15 September 2003; 162 (6): 1079–1088. doi: https://doi.org/10.1083/jcb.200303023
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