Skip to main content
NCBI home page
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1996 Oct 29;93(22):12076–12077. doi: 10.1073/pnas.93.22.12076

Anaphase in vitro.

W Z Cande 1, H J Wein 1
PMCID: PMC37944  PMID: 8901534

Full text

PDF
12076

Images in this article

12077Fig. 1
on p.12077

Selected References

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

  1. Boleti H., Karsenti E., Vernos I. Xklp2, a novel Xenopus centrosomal kinesin-like protein required for centrosome separation during mitosis. Cell. 1996 Jan 12;84(1):49–59. doi: 10.1016/s0092-8674(00)80992-7. [DOI] [PubMed] [Google Scholar]
  2. Cande W. Z., McDonald K. L. In vitro reactivation of anaphase spindle elongation using isolated diatom spindles. Nature. 1985 Jul 11;316(6024):168–170. doi: 10.1038/316168a0. [DOI] [PubMed] [Google Scholar]
  3. Cande W. Z. Nucleotide requirements for anaphase chromosome movements in permeabilized mitotic cells: anaphase B but not anaphase A requires ATP. Cell. 1982 Jan;28(1):15–22. doi: 10.1016/0092-8674(82)90370-1. [DOI] [PubMed] [Google Scholar]
  4. Hogan C. J., Wein H., Wordeman L., Scholey J. M., Sawin K. E., Cande W. Z. Inhibition of anaphase spindle elongation in vitro by a peptide antibody that recognizes kinesin motor domain. Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6611–6615. doi: 10.1073/pnas.90.14.6611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Inoué S., Salmon E. D. Force generation by microtubule assembly/disassembly in mitosis and related movements. Mol Biol Cell. 1995 Dec;6(12):1619–1640. doi: 10.1091/mbc.6.12.1619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. KANE R. E. THE MITOTIC APPARATUS. PHYSICAL-CHEMICAL FACTORS CONTROLLING STABILITY. J Cell Biol. 1965 Apr;25:SUPPL–SUPPL:144. doi: 10.1083/jcb.25.1.137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lohka M. J., Maller J. L. Induction of nuclear envelope breakdown, chromosome condensation, and spindle formation in cell-free extracts. J Cell Biol. 1985 Aug;101(2):518–523. doi: 10.1083/jcb.101.2.518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mazia D., Dan K. The Isolation and Biochemical Characterization of the Mitotic Apparatus of Dividing Cells. Proc Natl Acad Sci U S A. 1952 Sep;38(9):826–838. doi: 10.1073/pnas.38.9.826. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. McIntosh J. R., Pfarr C. M. Mitotic motors. J Cell Biol. 1991 Nov;115(3):577–585. doi: 10.1083/jcb.115.3.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Murray A. W., Desai A. B., Salmon E. D. Real time observation of anaphase in vitro. Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12327–12332. doi: 10.1073/pnas.93.22.12327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nislow C., Lombillo V. A., Kuriyama R., McIntosh J. R. A plus-end-directed motor enzyme that moves antiparallel microtubules in vitro localizes to the interzone of mitotic spindles. Nature. 1992 Oct 8;359(6395):543–547. doi: 10.1038/359543a0. [DOI] [PubMed] [Google Scholar]
  12. Palazzo R. E., Lutz D. A., Rebhun L. I. Reactivation of isolated mitotic apparatus: metaphase versus anaphase spindles. Cell Motil Cytoskeleton. 1991;18(4):304–318. doi: 10.1002/cm.970180407. [DOI] [PubMed] [Google Scholar]
  13. Pickett-Heaps J. D., Tippit D. H. The diatom spindle in perspective. Cell. 1978 Jul;14(3):455–467. doi: 10.1016/0092-8674(78)90232-5. [DOI] [PubMed] [Google Scholar]
  14. 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]
  15. 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]
  16. Walczak C. E., Mitchison T. J., Desai A. XKCM1: a Xenopus kinesin-related protein that regulates microtubule dynamics during mitotic spindle assembly. Cell. 1996 Jan 12;84(1):37–47. doi: 10.1016/s0092-8674(00)80991-5. [DOI] [PubMed] [Google Scholar]
  17. Watanabe N., Hunt T., Ikawa Y., Sagata N. Independent inactivation of MPF and cytostatic factor (Mos) upon fertilization of Xenopus eggs. Nature. 1991 Jul 18;352(6332):247–248. doi: 10.1038/352247a0. [DOI] [PubMed] [Google Scholar]
  18. Wein H., Foss M., Brady B., Cande W. Z. DSK1, a novel kinesin-related protein from the diatom Cylindrotheca fusiformis that is involved in anaphase spindle elongation. J Cell Biol. 1996 May;133(3):595–604. doi: 10.1083/jcb.133.3.595. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES