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Published online
doi:10.1083/jcb.200806185
The Journal of Cell Biology, Vol. 184, No. 2, 269-280
The Rockefeller University Press, 0021-9525 $30.00
© Staiger et al.
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Article

Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array



Christopher J. Staiger1,2, Michael B. Sheahan3,4, Parul Khurana1, Xia Wang1, David W. McCurdy3, and Laurent Blanchoin5

1 Department of Biological Sciences and 2 The Bindley Bioscience Center, Hansen Life Sciences Research Building, Purdue University, West Lafayette, IN 47907
3 Plant Science Group, School of Environmental and Life Sciences, The University of Newcastle, Callahan, NSW 2308, Australia
4 ARC Centre of Excellence for Integrative Legume Research, The University of Newcastle, Callahan, NSW 2308, Australia
5 Institut de Recherches en Technologie et Sciences pour le Vivant – iRTSV, Laboratoire de Physiologie Cellulaire Végétale, Commissariat à l'Energie Atomique/Centre National de la Recherche Scientifique/Institut National de la Recherche Agronomique/Université Joseph Fourier, CEA Grenoble, F38054 Grenoble, France

Correspondence to Christopher J. Staiger: staiger{at}purdue.edu; or Laurent Blanchoin: laurent.blanchoin{at}cea.fr

Metazoan cells harness the power of actin dynamics to create cytoskeletal arrays that stimulate protrusions and drive intracellular organelle movements. In plant cells, the actin cytoskeleton is understood to participate in cell elongation; however, a detailed description and molecular mechanism(s) underpinning filament nucleation, growth, and turnover are lacking. Here, we use variable-angle epifluorescence microscopy (VAEM) to examine the organization and dynamics of the cortical cytoskeleton in growing and nongrowing epidermal cells. One population of filaments in the cortical array, which most likely represent single actin filaments, is randomly oriented and highly dynamic. These filaments grow at rates of 1.7 µm/s, but are generally short-lived. Instead of depolymerization at their ends, actin filaments are disassembled by severing activity. Remodeling of the cortical actin array also features filament buckling and straightening events. These observations indicate a mechanism inconsistent with treadmilling. Instead, cortical actin filament dynamics resemble the stochastic dynamics of an in vitro biomimetic system for actin assembly.


Abbreviations used in this paper: BDM, 2,3-butanedione monoxime; fABD2, second actin-binding domain of Arabidopsis FIMBRIN1; FFP, fluorescent fusion protein; G-actin, monomeric actin; LatB, latrunculin B; TIRFM, total internal reflection fluorescence microscopy; VAEM, variable-angle epifluorescence microscopy.

© 2009 Staiger et al.
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