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. 1996 May 1;133(3):585–593. doi: 10.1083/jcb.133.3.585

Cell cycle regulation of dynein association with membranes modulates microtubule-based organelle transport

PMCID: PMC2120815  PMID: 8636233

Abstract

Cytoplasmic dynein is a minus end-directed microtubule motor that performs distinct functions in interphase and mitosis. In interphase, dynein transports organelles along microtubules, whereas in metaphase this motor has been implicated in mitotic spindle formation and orientation as well as chromosome segregation. The manner in which dynein activity is regulated during the cell cycle, however, has not been resolved. In this study, we have examined the mechanism by which organelle transport is controlled by the cell cycle in extracts of Xenopus laevis eggs. Here, we show that photocleavage of the dynein heavy chain dramatically inhibits minus end-directed organelle transport and that purified dynein restores this motility, indicating that dynein is the predominant minus end-directed membrane motor in Xenopus egg extracts. By measuring the amount of dynein associated with isolated membranes, we find that cytoplasmic dynein and its activator dynactin detach from the membrane surface in metaphase extracts. The sevenfold decrease in membrane-associated dynein correlated well with the eightfold reduction in minus end-directed membrane transport observed in metaphase versus interphase extracts. Although dynein heavy or intermediate chain phosphorylation did not change in a cell cycle- dependent manner, the dynein light intermediate chain incorporated approximately 12-fold more radiolabeled phosphate in metaphase than in interphase extracts. These studies suggest that cell cycle-dependent phosphorylation of cytoplasmic dynein may regulate organelle transport by modulating the association of this motor with membranes.

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Selected References

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  1. Allan V. J., Vale R. D. Cell cycle control of microtubule-based membrane transport and tubule formation in vitro. J Cell Biol. 1991 Apr;113(2):347–359. doi: 10.1083/jcb.113.2.347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Allan V. Protein phosphatase 1 regulates the cytoplasmic dynein-driven formation of endoplasmic reticulum networks in vitro. J Cell Biol. 1995 Mar;128(5):879–891. doi: 10.1083/jcb.128.5.879. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Brady S. T. A novel brain ATPase with properties expected for the fast axonal transport motor. Nature. 1985 Sep 5;317(6032):73–75. doi: 10.1038/317073a0. [DOI] [PubMed] [Google Scholar]
  4. Dillman J. F., 3rd, Pfister K. K. Differential phosphorylation in vivo of cytoplasmic dynein associated with anterogradely moving organelles. J Cell Biol. 1994 Dec;127(6 Pt 1):1671–1681. doi: 10.1083/jcb.127.6.1671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Echeverri C. J., Paschal B. M., Vaughan K. T., Vallee R. B. Molecular characterization of the 50-kD subunit of dynactin reveals function for the complex in chromosome alignment and spindle organization during mitosis. J Cell Biol. 1996 Feb;132(4):617–633. doi: 10.1083/jcb.132.4.617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Eshel D., Urrestarazu L. A., Vissers S., Jauniaux J. C., van Vliet-Reedijk J. C., Planta R. J., Gibbons I. R. Cytoplasmic dynein is required for normal nuclear segregation in yeast. Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):11172–11176. doi: 10.1073/pnas.90.23.11172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gibbons I. R., Lee-Eiford A., Mocz G., Phillipson C. A., Tang W. J., Gibbons B. H. Photosensitized cleavage of dynein heavy chains. Cleavage at the "V1 site" by irradiation at 365 nm in the presence of ATP and vanadate. J Biol Chem. 1987 Feb 25;262(6):2780–2786. [PubMed] [Google Scholar]
  8. Gill S. R., Cleveland D. W., Schroer T. A. Characterization of DLC-A and DLC-B, two families of cytoplasmic dynein light chain subunits. Mol Biol Cell. 1994 Jun;5(6):645–654. doi: 10.1091/mbc.5.6.645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gill S. R., Schroer T. A., Szilak I., Steuer E. R., Sheetz M. P., Cleveland D. W. Dynactin, a conserved, ubiquitously expressed component of an activator of vesicle motility mediated by cytoplasmic dynein. J Cell Biol. 1991 Dec;115(6):1639–1650. doi: 10.1083/jcb.115.6.1639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hamm-Alvarez S. F., Kim P. Y., Sheetz M. P. Regulation of vesicle transport in CV-1 cells and extracts. J Cell Sci. 1993 Nov;106(Pt 3):955–966. doi: 10.1242/jcs.106.3.955. [DOI] [PubMed] [Google Scholar]
  11. Hollenbeck P. J. Phosphorylation of neuronal kinesin heavy and light chains in vivo. J Neurochem. 1993 Jun;60(6):2265–2275. doi: 10.1111/j.1471-4159.1993.tb03513.x. [DOI] [PubMed] [Google Scholar]
  12. Hollenbeck P. J., Swanson J. A. Radial extension of macrophage tubular lysosomes supported by kinesin. Nature. 1990 Aug 30;346(6287):864–866. doi: 10.1038/346864a0. [DOI] [PubMed] [Google Scholar]
  13. Hughes S. M., Vaughan K. T., Herskovits J. S., Vallee R. B. Molecular analysis of a cytoplasmic dynein light intermediate chain reveals homology to a family of ATPases. J Cell Sci. 1995 Jan;108(Pt 1):17–24. doi: 10.1242/jcs.108.1.17. [DOI] [PubMed] [Google Scholar]
  14. Karki S., Holzbaur E. L. Affinity chromatography demonstrates a direct binding between cytoplasmic dynein and the dynactin complex. J Biol Chem. 1995 Dec 1;270(48):28806–28811. doi: 10.1074/jbc.270.48.28806. [DOI] [PubMed] [Google Scholar]
  15. King S. M., Wilkerson C. G., Witman G. B. The Mr 78,000 intermediate chain of Chlamydomonas outer arm dynein interacts with alpha-tubulin in situ. J Biol Chem. 1991 May 5;266(13):8401–8407. [PubMed] [Google Scholar]
  16. King S. M., Witman G. B. Localization of an intermediate chain of outer arm dynein by immunoelectron microscopy. J Biol Chem. 1990 Nov 15;265(32):19807–19811. [PubMed] [Google Scholar]
  17. Koonce M. P., Grissom P. M., McIntosh J. R. Dynein from Dictyostelium: primary structure comparisons between a cytoplasmic motor enzyme and flagellar dynein. J Cell Biol. 1992 Dec;119(6):1597–1604. doi: 10.1083/jcb.119.6.1597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kotz K. J., McNiven M. A. Intracellular calcium and cAMP regulate directional pigment movements in teleost erythrophores. J Cell Biol. 1994 Feb;124(4):463–474. doi: 10.1083/jcb.124.4.463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  20. Lee-Eiford A., Ow R. A., Gibbons I. R. Specific cleavage of dynein heavy chains by ultraviolet irradiation in the presence of ATP and vanadate. J Biol Chem. 1986 Feb 15;261(5):2337–2342. [PubMed] [Google Scholar]
  21. Lee K. D., Hollenbeck P. J. Phosphorylation of kinesin in vivo correlates with organelle association and neurite outgrowth. J Biol Chem. 1995 Mar 10;270(10):5600–5605. doi: 10.1074/jbc.270.10.5600. [DOI] [PubMed] [Google Scholar]
  22. Li Y. Y., Yeh E., Hays T., Bloom K. Disruption of mitotic spindle orientation in a yeast dynein mutant. Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):10096–10100. doi: 10.1073/pnas.90.21.10096. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Lin S. X., Ferro K. L., Collins C. A. Cytoplasmic dynein undergoes intracellular redistribution concomitant with phosphorylation of the heavy chain in response to serum starvation and okadaic acid. J Cell Biol. 1994 Nov;127(4):1009–1019. doi: 10.1083/jcb.127.4.1009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Lynch T. J., Taylor J. D., Tchen T. T. Regulation of pigment organelle translocation. I. Phosphorylation of the organelle-associated protein p57. J Biol Chem. 1986 Mar 25;261(9):4204–4211. [PubMed] [Google Scholar]
  25. Lynch T. J., Wu B. Y., Taylor J. D., Tchen T. T. Regulation of pigment organelle translocation. II. Participation of a cAMP-dependent protein kinase. J Biol Chem. 1986 Mar 25;261(9):4212–4216. [PubMed] [Google Scholar]
  26. Matthies H. J., Miller R. J., Palfrey H. C. Calmodulin binding to and cAMP-dependent phosphorylation of kinesin light chains modulate kinesin ATPase activity. J Biol Chem. 1993 May 25;268(15):11176–11187. [PubMed] [Google Scholar]
  27. McIlvain J. M., Jr, Burkhardt J. K., Hamm-Alvarez S., Argon Y., Sheetz M. P. Regulation of kinesin activity by phosphorylation of kinesin-associated proteins. J Biol Chem. 1994 Jul 22;269(29):19176–19182. [PubMed] [Google Scholar]
  28. Melloni R. H., Jr, Tokito M. K., Holzbaur E. L. Expression of the p150Glued component of the dynactin complex in developing and adult rat brain. J Comp Neurol. 1995 Jun 19;357(1):15–24. doi: 10.1002/cne.903570103. [DOI] [PubMed] [Google Scholar]
  29. Mitchell D. R., Rosenbaum J. L. Protein-protein interactions in the 18S ATPase of Chlamydomonas outer dynein arms. Cell Motil Cytoskeleton. 1986;6(5):510–520. doi: 10.1002/cm.970060510. [DOI] [PubMed] [Google Scholar]
  30. Muhua L., Karpova T. S., Cooper J. A. A yeast actin-related protein homologous to that in vertebrate dynactin complex is important for spindle orientation and nuclear migration. Cell. 1994 Aug 26;78(4):669–679. doi: 10.1016/0092-8674(94)90531-2. [DOI] [PubMed] [Google Scholar]
  31. Murray A. W. Cell cycle extracts. Methods Cell Biol. 1991;36:581–605. [PubMed] [Google Scholar]
  32. Murray A. W., Solomon M. J., Kirschner M. W. The role of cyclin synthesis and degradation in the control of maturation promoting factor activity. Nature. 1989 May 25;339(6222):280–286. doi: 10.1038/339280a0. [DOI] [PubMed] [Google Scholar]
  33. Niclas J., Navone F., Hom-Booher N., Vale R. D. Cloning and localization of a conventional kinesin motor expressed exclusively in neurons. Neuron. 1994 May;12(5):1059–1072. doi: 10.1016/0896-6273(94)90314-x. [DOI] [PubMed] [Google Scholar]
  34. Okada Y., Sato-Yoshitake R., Hirokawa N. The activation of protein kinase A pathway selectively inhibits anterograde axonal transport of vesicles but not mitochondria transport or retrograde transport in vivo. J Neurosci. 1995 Apr;15(4):3053–3064. doi: 10.1523/JNEUROSCI.15-04-03053.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Palazzo R. E., Vaisberg E., Cole R. W., Rieder C. L. Centriole duplication in lysates of Spisula solidissima oocytes. Science. 1992 Apr 10;256(5054):219–221. doi: 10.1126/science.1566068. [DOI] [PubMed] [Google Scholar]
  36. Paschal B. M., Mikami A., Pfister K. K., Vallee R. B. Homology of the 74-kD cytoplasmic dynein subunit with a flagellar dynein polypeptide suggests an intracellular targeting function. J Cell Biol. 1992 Sep;118(5):1133–1143. doi: 10.1083/jcb.118.5.1133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Paschal B. M., Shpetner H. S., Vallee R. B. MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties. J Cell Biol. 1987 Sep;105(3):1273–1282. doi: 10.1083/jcb.105.3.1273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Paschal B. M., Vallee R. B. Retrograde transport by the microtubule-associated protein MAP 1C. Nature. 1987 Nov 12;330(6144):181–183. doi: 10.1038/330181a0. [DOI] [PubMed] [Google Scholar]
  39. Pfarr C. M., Coue M., Grissom P. M., Hays T. S., Porter M. E., McIntosh J. R. Cytoplasmic dynein is localized to kinetochores during mitosis. Nature. 1990 May 17;345(6272):263–265. doi: 10.1038/345263a0. [DOI] [PubMed] [Google Scholar]
  40. Plamann M., Minke P. F., Tinsley J. H., Bruno K. S. Cytoplasmic dynein and actin-related protein Arp1 are required for normal nuclear distribution in filamentous fungi. J Cell Biol. 1994 Oct;127(1):139–149. doi: 10.1083/jcb.127.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Rodionov V. I., Gyoeva F. K., Gelfand V. I. Kinesin is responsible for centrifugal movement of pigment granules in melanophores. Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4956–4960. doi: 10.1073/pnas.88.11.4956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Rozdzial M. M., Haimo L. T. Bidirectional pigment granule movements of melanophores are regulated by protein phosphorylation and dephosphorylation. Cell. 1986 Dec 26;47(6):1061–1070. doi: 10.1016/0092-8674(86)90821-4. [DOI] [PubMed] [Google Scholar]
  43. Saunders W. S., Koshland D., Eshel D., Gibbons I. R., Hoyt M. A. Saccharomyces cerevisiae kinesin- and dynein-related proteins required for anaphase chromosome segregation. J Cell Biol. 1995 Feb;128(4):617–624. doi: 10.1083/jcb.128.4.617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Schnapp B. J., Reese T. S. Dynein is the motor for retrograde axonal transport of organelles. Proc Natl Acad Sci U S A. 1989 Mar;86(5):1548–1552. doi: 10.1073/pnas.86.5.1548. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Schroer T. A., Sheetz M. P. Two activators of microtubule-based vesicle transport. J Cell Biol. 1991 Dec;115(5):1309–1318. doi: 10.1083/jcb.115.5.1309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Schroer T. A., Steuer E. R., Sheetz M. P. Cytoplasmic dynein is a minus end-directed motor for membranous organelles. Cell. 1989 Mar 24;56(6):937–946. doi: 10.1016/0092-8674(89)90627-2. [DOI] [PubMed] [Google Scholar]
  47. Steuer E. R., Wordeman L., Schroer T. A., Sheetz M. P. Localization of cytoplasmic dynein to mitotic spindles and kinetochores. Nature. 1990 May 17;345(6272):266–268. doi: 10.1038/345266a0. [DOI] [PubMed] [Google Scholar]
  48. Thaler C. D., Haimo L. T. Regulation of organelle transport in melanophores by calcineurin. J Cell Biol. 1990 Nov;111(5 Pt 1):1939–1948. doi: 10.1083/jcb.111.5.1939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Vaisberg E. A., Koonce M. P., McIntosh J. R. Cytoplasmic dynein plays a role in mammalian mitotic spindle formation. J Cell Biol. 1993 Nov;123(4):849–858. doi: 10.1083/jcb.123.4.849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Vale R. D., Reese T. S., Sheetz M. P. Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility. Cell. 1985 Aug;42(1):39–50. doi: 10.1016/s0092-8674(85)80099-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Vaughan K. T., Vallee R. B. Cytoplasmic dynein binds dynactin through a direct interaction between the intermediate chains and p150Glued. J Cell Biol. 1995 Dec;131(6 Pt 1):1507–1516. doi: 10.1083/jcb.131.6.1507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Verde F., Berrez J. M., Antony C., Karsenti E. Taxol-induced microtubule asters in mitotic extracts of Xenopus eggs: requirement for phosphorylated factors and cytoplasmic dynein. J Cell Biol. 1991 Mar;112(6):1177–1187. doi: 10.1083/jcb.112.6.1177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Warren G., Davoust J., Cockcroft A. Recycling of transferrin receptors in A431 cells is inhibited during mitosis. EMBO J. 1984 Oct;3(10):2217–2225. doi: 10.1002/j.1460-2075.1984.tb02119.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Warren G., Featherstone C., Griffiths G., Burke B. Newly synthesized G protein of vesicular stomatitis virus is not transported to the cell surface during mitosis. J Cell Biol. 1983 Nov;97(5 Pt 1):1623–1628. doi: 10.1083/jcb.97.5.1623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Warren G., Wickner W. Organelle inheritance. Cell. 1996 Feb 9;84(3):395–400. doi: 10.1016/s0092-8674(00)81284-2. [DOI] [PubMed] [Google Scholar]
  57. Xiang X., Beckwith S. M., Morris N. R. Cytoplasmic dynein is involved in nuclear migration in Aspergillus nidulans. Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2100–2104. doi: 10.1073/pnas.91.6.2100. [DOI] [PMC free article] [PubMed] [Google Scholar]

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