Dynactin links cytoplasmic dynein and other motors to cargo and is involved in organizing radial microtubule arrays. The largest subunit of dynactin, p150glued, binds the dynein intermediate chain and has an N-terminal microtubule-binding domain. To examine the role of microtubule binding by p150glued, we replaced the wild-type p150glued in Drosophila melanogaster S2 cells with mutant ΔN-p150 lacking residues 1–200, which is unable to bind microtubules. Cells treated with cytochalasin D were used for analysis of cargo movement along microtubules. Strikingly, although the movement of both membranous organelles and messenger ribonucleoprotein complexes by dynein and kinesin-1 requires dynactin, the substitution of full-length p150glued with ΔN-p150glued has no effect on the rate, processivity, or step size of transport. However, truncation of the microtubule-binding domain of p150glued has a dramatic effect on cell division, resulting in the generation of multipolar spindles and free microtubule-organizing centers. Thus, dynactin binding to microtubules is required for organizing spindle microtubule arrays but not cargo motility in vivo.
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26 February 2007
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February 26 2007
Microtubule binding by dynactin is required for microtubule organization but not cargo transport
Hwajin Kim,
Hwajin Kim
1Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611
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Shuo-Chien Ling,
Shuo-Chien Ling
1Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611
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Gregory C. Rogers,
Gregory C. Rogers
2Department of Biology, University of North Carolina, Chapel Hill, NC 27599
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Paul R. Selvin,
Paul R. Selvin
3Biophysics Center
4Physics Department, University of Illinois, Urbana, IL 61801
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Stephen L. Rogers,
Stephen L. Rogers
2Department of Biology, University of North Carolina, Chapel Hill, NC 27599
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Vladimir I. Gelfand
Vladimir I. Gelfand
1Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611
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Hwajin Kim
1Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611
Shuo-Chien Ling
1Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611
Gregory C. Rogers
2Department of Biology, University of North Carolina, Chapel Hill, NC 27599
Comert Kural
3Biophysics Center
Paul R. Selvin
3Biophysics Center
4Physics Department, University of Illinois, Urbana, IL 61801
Stephen L. Rogers
2Department of Biology, University of North Carolina, Chapel Hill, NC 27599
Vladimir I. Gelfand
1Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611
Correspondence to Vladimir I. Gelfand: [email protected]
Abbreviations used in this paper: dFMRP, Drosophila homologue of the fragile X mental retardation protein; DHC, dynein heavy chain; KHC, kinesin heavy chain; mRFP, monomeric red fluorescent protein; mRNP, messenger RNP; MTOC, microtubule-organizing center; UTR, untranslated region.
Received:
August 21 2006
Accepted:
January 24 2007
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2007
J Cell Biol (2007) 176 (5): 641–651.
Article history
Received:
August 21 2006
Accepted:
January 24 2007
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Citation
Hwajin Kim, Shuo-Chien Ling, Gregory C. Rogers, Comert Kural, Paul R. Selvin, Stephen L. Rogers, Vladimir I. Gelfand; Microtubule binding by dynactin is required for microtubule organization but not cargo transport . J Cell Biol 26 February 2007; 176 (5): 641–651. doi: https://doi.org/10.1083/jcb.200608128
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