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filaments are important ways to induce actin assembly in response to signals.
However, in the past five years, we have gained an understanding of how the
WASp-Arp2/3 pathway, together with Ena/VASP proteins, can mediate actin
assembly in dynamic cell structures. Recent evidence indicates that there are
other ways to nucleate filament networks independently of the Arp2/3
complex, such as through the formins. As time progresses, we will hopefully
develop a deeper understanding of how the different systems for generating
actin filaments work together and thus a better idea of how the extremely
complex processes of cell movement and shape changes are regulated. No
doubt the next five years will also bring some new surprises and additional
players to the field - we can only look forward to a clearer, if more detailed,
picture of how actin dynamics allows cells to move and adapt to their
environment.
References
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directly to a protein implicated in the immunodeficiency disorder Wiskott-Aldrich
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Benesch, S., Lommel, S., Steffen, A., Stradal, T. E., et al., 2002. Phosphatidylinositol 4,5-
biphosphate (PIP2)-induced vesicle movement depends on N-WASP and involves Nck,
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Carlier, M. F., Nioche, P., Broutin-L'Hermite, I., Boujemaa, R., et al., 2000. GRB2 links
signaling to actin assembly by enhancing interaction of neural Wiskott-Aldrich
syndrome protein (N-WASp) with actin-related protein (ARP2/3) complex. J. Biol.
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