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PMID: 2295685 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Kinetochores are transported poleward along a single astral microtubule during chromosome attachment to the spindle in newt lung cells.

The Journal of cell biology ·Vol. 110 ·No. 1 ·1990-01-00 ·Pages 81-95

Rieder CL, Alexander SP

Abstract

During mitosis in cultured newt pneumocytes, one or more chromosomes may become positioned well removed (greater than 50 microns) from the polar regions during early prometaphase. As a result, these chromosomes are delayed for up to 5 h in forming an attachment to the spindle. The spatial separation of these chromosomes from the polar microtubule-nucleating centers provides a unique opportunity to study the initial stages of kinetochore fiber formation in living cells. Time-lapse Nomarski-differential interference contrast videomicroscopic observations reveal that late-attaching chromosomes always move, upon attachment, into a single polar region (usually the one closest to the chromosome). During this attachment, the kinetochore region of the chromosome undergoes a variable number of transient poleward tugs that are followed, shortly thereafter, by rapid movement of the chromosome towards the pole. Anti-tubulin immunofluorescence and serial section EM reveal that the kinetochores and kinetochore regions of nonattached chromosomes lack associated microtubules. By contrast, these methods reveal that the attachment and subsequent poleward movement of a chromosome correlates with the association of a single long microtubule with one of the kinetochores of the chromosome. This microtubule traverses the entire distance between the spindle pole and the kinetochore and often extends well past the kinetochore. From these results, we conclude that the initial attachment of a chromosome to the newt pneumocyte spindle results from an interaction between a single polar-nucleated microtubule and one of the kinetochores on the chromosome. Once this association is established, the kinetochore is rapidly transported poleward along the surface of the microtubule by a mechanism that is not dependent on microtubule depolymerization. Our results further demonstrate that the motors for prometaphase chromosome movement must be either on the surface of the kinetochore (i.e., within the corona but not the plate), distributed along the surface of the kinetochore microtubules, or both.

MeSH Terms
Animals Cells, Cultured Centromere/physiology,ultrastructure Chromosomes/physiology,ultrastructure Lung/cytology,ultrastructure Microscopy, Electron Mitosis Models, Structural Salamandridae Spindle Apparatus/physiology,ultrastructure
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Rieder C L
Wadsworth Center for Laboratories and Research, Albany, New York 12201-0509.
Alexander S P
References (53)
53 references, click to expand
  1. Microtubule dynamics in the chromosomal spindle fiber: analysis by fluorescence and high-resolution polarization microscopy.
    Cell Motil Cytoskeleton. 1988;10(1-2):185-96 PMID: 3180243
  2. The forces that move chromosomes in mitosis.
    Annu Rev Biophys Biophys Chem. 1988;17:431-49 PMID: 3293594
  3. Microtubule dynamics and kinetochore function in mitosis.
    Annu Rev Cell Biol. 1988;4:527-49 PMID: 3058165
  4. Real-time observations of microtubule dynamic instability in living cells.
    J Cell Biol. 1988 Dec;107(6 Pt 1):2223-31 PMID: 3198684
  5. Three-dimensional reconstruction of cells from serial sections and whole-cell mounts using multilevel contouring of stereo micrographs.
    J Electron Microsc Tech. 1988 Aug;9(4):395-411 PMID: 2462031
  6. Asymmetric behavior of severed microtubule ends after ultraviolet-microbeam irradiation of individual microtubules in vitro.
    J Cell Biol. 1989 Mar;108(3):931-7 PMID: 2921286
  7. Microtubule dynamics investigated by microinjection of Paramecium axonemal tubulin: lack of nucleation but proximal assembly of microtubules at the kinetochore during prometaphase.
    J Cell Biol. 1989 Mar;108(3):939-53 PMID: 2646309
  8. Do anaphase chromosomes chew their way to the pole or are they pulled by actin?
    J Cell Sci. 1988 Dec;91 ( Pt 4):449-53 PMID: 3255751
  9. Light and electron microscopy of rat kangaroo cells in mitosis. II. Kinetochore structure and function.
    Chromosoma. 1973;41(2):195-220 PMID: 4571311
  10. Spindle microtubule dynamics in sea urchin embryos: analysis using a fluorescein-labeled tubulin and measurements of fluorescence redistribution after laser photobleaching.
    J Cell Biol. 1984 Dec;99(6):2165-74 PMID: 6501418
  11. Dynamic instability of microtubule growth.
    Nature. 1984 Nov 15-21;312(5991):237-42 PMID: 6504138
  12. Experimental separation of pronuclei in fertilized sea urchin eggs: chromosomes do not organize a spindle in the absence of centrosomes.
    J Cell Biol. 1985 Mar;100(3):897-903 PMID: 3972900
  13. Properties of the kinetochore in vitro. I. Microtubule nucleation and tubulin binding.
    J Cell Biol. 1985 Sep;101(3):755-65 PMID: 4030893
  14. Properties of the kinetochore in vitro. II. Microtubule capture and ATP-dependent translocation.
    J Cell Biol. 1985 Sep;101(3):766-77 PMID: 4030894
  15. Microtubules, chromosome movement, and reorientation after chromosomes are detached from the spindle by micromanipulation.
    Chromosoma. 1985;92(4):313-24 PMID: 4042772
  16. Chromosome micromanipulation. II. Induced reorientation and the experimental control of segregation in meiosis.
    Chromosoma. 1967;21(1):17-50 PMID: 6029962
  17. Biotin-tubulin incorporates into kinetochore fiber microtubules during early but not late anaphase.
    J Cell Biol. 1989 Nov;109(5):2257-65 PMID: 2681228
  18. Prophase chromosome movements in living house cricket spermatocytes and their relationship to prometaphase, anaphase and granule movements.
    Chromosoma. 1975;49(4):407-55 PMID: 1132283
  19. Studies on the mechanism of mitosis.
    Ann N Y Acad Sci. 1975 Jun 30;253:407-27 PMID: 1056752
  20. Cold-labile and cold-stable microtubules in the mitotic spindle of mammalian cells.
    Ann N Y Acad Sci. 1975 Jun 30;253:428-39 PMID: 1056753
  21. Structure and physiology of the mammalian mitotic spindle.
    Soc Gen Physiol Ser. 1975;30:31-76 PMID: 1103303
  22. Assembly of microtubules onto kinetochores of isolated mitotic chromosomes of HeLa cells.
    Proc Natl Acad Sci U S A. 1975 Oct;72(10):4023-7 PMID: 1060085
  23. Light and electron microscopy of rat kangaroo cells in mitosis. III. Patterns of chromosome behavior during prometaphase.
    Chromosoma. 1976 Mar 10;54(4):363-85 PMID: 1253643
  24. Mitotic mechanism based on intrinsic microtubule behaviour.
    Nature. 1978 Mar 30;272(5652):450-2 PMID: 634367
  25. The diatom spindle in perspective.
    Cell. 1978 Jul;14(3):455-67 PMID: 357008
  26. Electron microscopy of spermatocytes previously studied in life: methods and some observations on micromanipulated chromosomes.
    J Cell Sci. 1979 Feb;35:87-104 PMID: 370131
  27. Cell division in two large pennate diatoms Hantzschia and Nitzschia III. A new proposal for kinetochore function during prometaphase.
    J Cell Biol. 1980 Aug;86(2):402-16 PMID: 7400213
  28. Mitosis in Oedogonium: spindle microfilaments and the origin of the kinetochore fiber.
    Eur J Cell Biol. 1980 Oct;22(2):687-98 PMID: 7192627
  29. Chromosome behavior after laser microirradiation of a single kinetochore in mitotic PtK2 cells.
    J Cell Biol. 1981 Mar;88(3):543-53 PMID: 7194343
  30. Structural polarity of kinetochore microtubules in PtK1 cells.
    J Cell Biol. 1981 May;89(2):338-45 PMID: 7251657
  31. Structural interaction of cytoskeletal components.
    J Cell Biol. 1981 Jul;90(1):222-35 PMID: 7019221
  32. The attachment of kinetochores to the pro-metaphase spindle in PtK1 cells. Recovery from low temperature treatment.
    Chromosoma. 1981;82(5):693-716 PMID: 7261715
  33. Kinetochore structure and its role in chromosome orientation during the first meiotic division in male D. melanogaster.
    Cell. 1981 Sep;25(3):591-602 PMID: 6793236
  34. The structure of the cold-stable kinetochore fiber in metaphase PtK1 cells.
    Chromosoma. 1981;84(1):145-58 PMID: 7297248
  35. Cell division and the mitotic spindle.
    J Cell Biol. 1981 Dec;91(3 Pt 2):131s-147s PMID: 7033235
  36. Functional autonomy of monopolar spindle and evidence for oscillatory movement in mitosis.
    J Cell Biol. 1982 Apr;93(1):33-48 PMID: 7068758
  37. Meiosis in Drosophila melanogaster. II. The prometaphase-I kinetochore microtubule bundle and kinetochore orientation in males.
    J Cell Biol. 1982 May;93(2):365-73 PMID: 6807996
  38. Traction force on a kinetochore at metaphase acts as a linear function of kinetochore fiber length.
    J Cell Biol. 1982 May;93(2):374-89 PMID: 7096444
  39. Bioenergetics and kinetics of microtubule and actin filament assembly-disassembly.
    Int Rev Cytol. 1982;78:1-125 PMID: 6128332
  40. Rethinking mitosis.
    Cell. 1982 Jul;29(3):729-44 PMID: 6217897
  41. The formation, structure, and composition of the mammalian kinetochore and kinetochore fiber.
    Int Rev Cytol. 1982;79:1-58 PMID: 6185450
  42. Measurements of the force produced by the mitotic spindle in anaphase.
    J Cell Biol. 1983 Aug;97(2):542-8 PMID: 6885908
  43. Malorientation in half-bivalents at anaphase: analysis of autosomal laggards in untreated, cold-treated, and cold-recovering crane fly spermatocytes.
    J Cell Biol. 1984 Mar;98(3):859-69 PMID: 6699088
  44. Aster-free spindle poles in insect spermatocytes: evidence for chromosome-induced spindle formation?
    J Cell Biol. 1986 May;102(5):1679-87 PMID: 3700473
  45. Sites of microtubule assembly and disassembly in the mitotic spindle.
    Cell. 1986 May 23;45(4):515-27 PMID: 3708686
  46. Oscillatory movements of monooriented chromosomes and their position relative to the spindle pole result from the ejection properties of the aster and half-spindle.
    J Cell Biol. 1986 Aug;103(2):581-91 PMID: 3733881
  47. Micromanipulated bivalents can trigger mini-spindle formation in Drosophila melanogaster spermatocyte cytoplasm.
    J Cell Biol. 1986 Dec;103(6 Pt 2):2765-73 PMID: 3098743
  48. Chromosomes move poleward in anaphase along stationary microtubules that coordinately disassemble from their kinetochore ends.
    J Cell Biol. 1987 Jan;104(1):9-18 PMID: 3793763
  49. Centrosome-kinetochore interaction in multinucleate cells.
    Chromosoma. 1987;95(2):136-43 PMID: 3595312
  50. MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties.
    J Cell Biol. 1987 Sep;105(3):1273-82 PMID: 2958482
  51. Retrograde transport by the microtubule-associated protein MAP 1C.
    Nature. 1987 Nov 12-18;330(6144):181-3 PMID: 3670402
  52. Polewards chromosome movement driven by microtubule depolymerization in vitro.
    Nature. 1988 Feb 11;331(6156):499-504 PMID: 3340202
  53. Dynein ATPases as microtubule motors.
    J Biol Chem. 1988 Nov 5;263(31):15837-40 PMID: 2972702
Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1990-01-00
Pages
81-95
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2115982
Subset
IM
Grants
PHS HHS · R01-40198 · United States
NCRR NIH HHS · RR 01219 · United States
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