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Vol. 18, Issue 6, 2081-2089, June 2007
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*Howard Hughes Medical Institute and Department of Cellular and Molecular Medicine, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0683;
Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037; and
Department of Physiology, University of Pennsylvania, Philadelphia, PA 19104
Submitted August 11, 2006;
Revised February 9, 2007;
Accepted March 2, 2007
Monitoring Editor: Yixian Zheng
Transport of cellular and neuronal vesicles, organelles, and other particles along microtubules requires the molecular motor protein dynein (Mallik and Gross, 2004). Critical to dynein function is dynactin, a multiprotein complex commonly thought to be required for dynein attachment to membrane compartments (Karki and Holzbaur, 1999). Recent work also has found that mutations in dynactin can cause the human motor neuron disease amyotrophic lateral sclerosis (Puls et al., 2003). Thus, it is essential to understand the in vivo function of dynactin. To test directly and rigorously the hypothesis that dynactin is required to attach dynein to membranes, we used both a Drosophila mutant and RNA interference to generate organisms and cells lacking the critical dynactin subunit, actin-related protein 1. Contrary to expectation, we found that apparently normal amounts of dynein associate with membrane compartments in the absence of a fully assembled dynactin complex. In addition, anterograde and retrograde organelle movement in dynactin deficient axons was completely disrupted, resulting in substantial changes in vesicle kinematic properties. Although effects on retrograde transport are predicted by the proposed function of dynactin as a regulator of dynein processivity, the additional effects we observed on anterograde transport also suggest potential roles for dynactin in mediating kinesin-driven transport and in coordinating the activity of opposing motors (King and Schroer, 2000).
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The online version of this article contains supplemental material at MBC Online (http://www.molbiolcell.org).
These authors contributed equally to this work.
Address correspondence to: Lawrence S.B. Goldstein (lgoldstein{at}ucsd.edu).
Abbreviations used: Arp1, actin-related protein 1; DHC, dynein heavy chain; KHC, kinesin heavy chain; p50, dynamitin; PNS, postnuclear supernatant; HSP, high-speed pellet; HSS, high-speed supernatant.
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