Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1995 Nov 1;131(3):693–708. doi: 10.1083/jcb.131.3.693

NuMA is required for the organization of microtubules into aster-like mitotic arrays

PMCID: PMC2120610  PMID: 7593190

Abstract

NuMA (Nuclear protein that associates with the Mitotic Apparatus) is a 235-kD intranuclear protein that accumulates at the pericentrosomal region of the mitotic spindle in vertebrate cells. To determine if NuMA plays an active role in organizing the microtubules at the polar region of the mitotic spindle, we have developed a cell free system for the assembly of mitotic asters derived from synchronized cultured cells. Mitotic asters assembled in this extract are composed of microtubules arranged in a radial array that contain NuMA concentrated at the central core. The organization of microtubules into asters in this cell free system is dependent on NuMA because immunodepletion of NuMA from the extract results in randomly dispersed microtubules instead of organized mitotic asters, and addition of the purified recombinant NuMA protein to the NuMA-depleted extract fully reconstitutes the organization of the microtubules into mitotic asters. Furthermore, we show that NuMA is phosphorylated upon mitotic aster assembly and that NuMA is only required in the late stages of aster assembly in this cell free system consistent with the temporal accumulation of NuMA at the polar ends of the mitotic spindle in vivo. These results, in combination with the phenotype observed in vivo after the prevention of NuMA from targeting onto the mitotic spindle by antibody microinjection, suggest that NuMA plays a functional role in the organization of the microtubules of the mitotic spindle.

Full Text

The Full Text of this article is available as a PDF (4.2 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Blose S. H., Meltzer D. I., Feramisco J. R. 10-nm filaments are induced to collapse in living cells microinjected with monoclonal and polyclonal antibodies against tubulin. J Cell Biol. 1984 Mar;98(3):847–858. doi: 10.1083/jcb.98.3.847. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Burke B., Gerace L. A cell free system to study reassembly of the nuclear envelope at the end of mitosis. Cell. 1986 Feb 28;44(4):639–652. doi: 10.1016/0092-8674(86)90273-4. [DOI] [PubMed] [Google Scholar]
  3. Capecchi M. R. High efficiency transformation by direct microinjection of DNA into cultured mammalian cells. Cell. 1980 Nov;22(2 Pt 2):479–488. doi: 10.1016/0092-8674(80)90358-x. [DOI] [PubMed] [Google Scholar]
  4. Cleveland D. W. NuMA: a protein involved in nuclear structure, spindle assembly, and nuclear re-formation. Trends Cell Biol. 1995 Feb;5(2):60–64. doi: 10.1016/s0962-8924(00)88947-3. [DOI] [PubMed] [Google Scholar]
  5. Compton D. A., Cleveland D. W. NuMA is required for the proper completion of mitosis. J Cell Biol. 1993 Feb;120(4):947–957. doi: 10.1083/jcb.120.4.947. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Compton D. A., Cleveland D. W. NuMA, a nuclear protein involved in mitosis and nuclear reformation. Curr Opin Cell Biol. 1994 Jun;6(3):343–346. doi: 10.1016/0955-0674(94)90024-8. [DOI] [PubMed] [Google Scholar]
  7. Compton D. A., Luo C. Mutation of the predicted p34cdc2 phosphorylation sites in NuMA impair the assembly of the mitotic spindle and block mitosis. J Cell Sci. 1995 Feb;108(Pt 2):621–633. doi: 10.1242/jcs.108.2.621. [DOI] [PubMed] [Google Scholar]
  8. Compton D. A., Szilak I., Cleveland D. W. Primary structure of NuMA, an intranuclear protein that defines a novel pathway for segregation of proteins at mitosis. J Cell Biol. 1992 Mar;116(6):1395–1408. doi: 10.1083/jcb.116.6.1395. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Compton D. A., Yen T. J., Cleveland D. W. Identification of novel centromere/kinetochore-associated proteins using monoclonal antibodies generated against human mitotic chromosome scaffolds. J Cell Biol. 1991 Mar;112(6):1083–1097. doi: 10.1083/jcb.112.6.1083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Doxsey S. J., Stein P., Evans L., Calarco P. D., Kirschner M. Pericentrin, a highly conserved centrosome protein involved in microtubule organization. Cell. 1994 Feb 25;76(4):639–650. doi: 10.1016/0092-8674(94)90504-5. [DOI] [PubMed] [Google Scholar]
  11. Félix M. A., Antony C., Wright M., Maro B. Centrosome assembly in vitro: role of gamma-tubulin recruitment in Xenopus sperm aster formation. J Cell Biol. 1994 Jan;124(1-2):19–31. doi: 10.1083/jcb.124.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gerace L., Burke B. Functional organization of the nuclear envelope. Annu Rev Cell Biol. 1988;4:335–374. doi: 10.1146/annurev.cb.04.110188.002003. [DOI] [PubMed] [Google Scholar]
  13. Joshi H. C., Palacios M. J., McNamara L., Cleveland D. W. Gamma-tubulin is a centrosomal protein required for cell cycle-dependent microtubule nucleation. Nature. 1992 Mar 5;356(6364):80–83. doi: 10.1038/356080a0. [DOI] [PubMed] [Google Scholar]
  14. Kallajoki M., Harborth J., Weber K., Osborn M. Microinjection of a monoclonal antibody against SPN antigen, now identified by peptide sequences as the NuMA protein, induces micronuclei in PtK2 cells. J Cell Sci. 1993 Jan;104(Pt 1):139–150. doi: 10.1242/jcs.104.1.139. [DOI] [PubMed] [Google Scholar]
  15. Kallajoki M., Weber K., Osborn M. A 210 kDa nuclear matrix protein is a functional part of the mitotic spindle; a microinjection study using SPN monoclonal antibodies. EMBO J. 1991 Nov;10(11):3351–3362. doi: 10.1002/j.1460-2075.1991.tb04899.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kallajoki M., Weber K., Osborn M. Ability to organize microtubules in taxol-treated mitotic PtK2 cells goes with the SPN antigen and not with the centrosome. J Cell Sci. 1992 May;102(Pt 1):91–102. doi: 10.1242/jcs.102.1.91. [DOI] [PubMed] [Google Scholar]
  17. 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]
  18. Lydersen B. K., Pettijohn D. E. Human-specific nuclear protein that associates with the polar region of the mitotic apparatus: distribution in a human/hamster hybrid cell. Cell. 1980 Nov;22(2 Pt 2):489–499. doi: 10.1016/0092-8674(80)90359-1. [DOI] [PubMed] [Google Scholar]
  19. Maekawa T., Kuriyama R. Differential pathways of recruitment for centrosomal antigens to the mitotic poles during bipolar spindle formation. J Cell Sci. 1991 Nov;100(Pt 3):533–540. doi: 10.1242/jcs.100.3.533. [DOI] [PubMed] [Google Scholar]
  20. Maekawa T., Kuriyama R. Primary structure and microtubule-interacting domain of the SP-H antigen: a mitotic MAP located at the spindle pole and characterized as a homologous protein to NuMA. J Cell Sci. 1993 Jun;105(Pt 2):589–600. doi: 10.1242/jcs.105.2.589. [DOI] [PubMed] [Google Scholar]
  21. Maekawa T., Leslie R., Kuriyama R. Identification of a minus end-specific microtubule-associated protein located at the mitotic poles in cultured mammalian cells. Eur J Cell Biol. 1991 Apr;54(2):255–267. [PubMed] [Google Scholar]
  22. McKeon F. Nuclear lamin proteins: domains required for nuclear targeting, assembly, and cell-cycle-regulated dynamics. Curr Opin Cell Biol. 1991 Feb;3(1):82–86. doi: 10.1016/0955-0674(91)90169-y. [DOI] [PubMed] [Google Scholar]
  23. Mitchison T. J. Mitosis: basic concepts. Curr Opin Cell Biol. 1989 Feb;1(1):67–74. doi: 10.1016/s0955-0674(89)80039-0. [DOI] [PubMed] [Google Scholar]
  24. Mitchison T. J. Polewards microtubule flux in the mitotic spindle: evidence from photoactivation of fluorescence. J Cell Biol. 1989 Aug;109(2):637–652. doi: 10.1083/jcb.109.2.637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Newport J. W., Forbes D. J. The nucleus: structure, function, and dynamics. Annu Rev Biochem. 1987;56:535–565. doi: 10.1146/annurev.bi.56.070187.002535. [DOI] [PubMed] [Google Scholar]
  26. Nicklas R. B., Lee G. M., Rieder C. L., Rupp G. Mechanically cut mitotic spindles: clean cuts and stable microtubules. J Cell Sci. 1989 Nov;94(Pt 3):415–423. doi: 10.1242/jcs.94.3.415. [DOI] [PubMed] [Google Scholar]
  27. Nigg E. A. Assembly-disassembly of the nuclear lamina. Curr Opin Cell Biol. 1992 Feb;4(1):105–109. doi: 10.1016/0955-0674(92)90066-l. [DOI] [PubMed] [Google Scholar]
  28. Pickett-Heaps J. D., Tippit D. H., Porter K. R. Rethinking mitosis. Cell. 1982 Jul;29(3):729–744. doi: 10.1016/0092-8674(82)90435-4. [DOI] [PubMed] [Google Scholar]
  29. Price C. M., Pettijohn D. E. Redistribution of the nuclear mitotic apparatus protein (NuMA) during mitosis and nuclear assembly. Properties of purified NuMA protein. Exp Cell Res. 1986 Oct;166(2):295–311. doi: 10.1016/0014-4827(86)90478-7. [DOI] [PubMed] [Google Scholar]
  30. Rebhun L. I., Palazzo R. E. In vitro reactivation of anaphase B in isolated spindles of the sea urchin egg. Cell Motil Cytoskeleton. 1988;10(1-2):197–209. doi: 10.1002/cm.970100124. [DOI] [PubMed] [Google Scholar]
  31. Rieder C. L. Mitosis: towards a molecular understanding of chromosome behavior. Curr Opin Cell Biol. 1991 Feb;3(1):59–66. doi: 10.1016/0955-0674(91)90166-v. [DOI] [PubMed] [Google Scholar]
  32. Sawin K. E., LeGuellec K., Philippe M., Mitchison T. J. Mitotic spindle organization by a plus-end-directed microtubule motor. Nature. 1992 Oct 8;359(6395):540–543. doi: 10.1038/359540a0. [DOI] [PubMed] [Google Scholar]
  33. Sawin K. E., Mitchison T. J. Microtubule flux in mitosis is independent of chromosomes, centrosomes, and antiparallel microtubules. Mol Biol Cell. 1994 Feb;5(2):217–226. doi: 10.1091/mbc.5.2.217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Sawin K. E., Mitchison T. J. Poleward microtubule flux mitotic spindles assembled in vitro. J Cell Biol. 1991 Mar;112(5):941–954. doi: 10.1083/jcb.112.5.941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Sluder G., Miller F. J., Rieder C. L. The reproduction of centrosomes: nuclear versus cytoplasmic controls. J Cell Biol. 1986 Nov;103(5):1873–1881. doi: 10.1083/jcb.103.5.1873. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Stearns T., Kirschner M. In vitro reconstitution of centrosome assembly and function: the central role of gamma-tubulin. Cell. 1994 Feb 25;76(4):623–637. doi: 10.1016/0092-8674(94)90503-7. [DOI] [PubMed] [Google Scholar]
  37. Tang T. K., Tang C. J., Chen Y. L., Wu C. W. Nuclear proteins of the bovine esophageal epithelium. II. The NuMA gene gives rise to multiple mRNAs and gene products reactive with monoclonal antibody W1. J Cell Sci. 1993 Feb;104(Pt 2):249–260. doi: 10.1242/jcs.104.2.249. [DOI] [PubMed] [Google Scholar]
  38. Tousson A., Zeng C., Brinkley B. R., Valdivia M. M. Centrophilin: a novel mitotic spindle protein involved in microtubule nucleation. J Cell Biol. 1991 Feb;112(3):427–440. doi: 10.1083/jcb.112.3.427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. 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]
  40. 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]
  41. Wiese C., Wilson K. L. Nuclear membrane dynamics. Curr Opin Cell Biol. 1993 Jun;5(3):387–394. doi: 10.1016/0955-0674(93)90002-8. [DOI] [PubMed] [Google Scholar]
  42. Yang C. H., Lambie E. J., Snyder M. NuMA: an unusually long coiled-coil related protein in the mammalian nucleus. J Cell Biol. 1992 Mar;116(6):1303–1317. doi: 10.1083/jcb.116.6.1303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Yang C. H., Snyder M. The nuclear-mitotic apparatus protein is important in the establishment and maintenance of the bipolar mitotic spindle apparatus. Mol Biol Cell. 1992 Nov;3(11):1259–1267. doi: 10.1091/mbc.3.11.1259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Zeng C., He D., Brinkley B. R. Localization of NuMA protein isoforms in the nuclear matrix of mammalian cells. Cell Motil Cytoskeleton. 1994;29(2):167–176. doi: 10.1002/cm.970290208. [DOI] [PubMed] [Google Scholar]
  45. Zhang D., Nicklas R. B. The impact of chromosomes and centrosomes on spindle assembly as observed in living cells. J Cell Biol. 1995 Jun;129(5):1287–1300. doi: 10.1083/jcb.129.5.1287. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES