Literature DB >> 6813060

Evidence for three "classes" of microtubules in the interpolar space of the mitotic micronucleus of a ciliate and the participation of the nuclear envelope in conferring stability to microtubules.

U Eichenlaub-Ritter, A Ruthmann.   

Abstract

Exposure of Nyctotherus ovalis to low temperatures or vinblastine caused similar reactions of "classes" of microtubules (mt) present in the mitotic micronucleus of this ciliate towards both treatments. However, differences of sensitivity between certain "classes" of mt at individual mitotic stages exist. Unlike the kinetochore mt (kmt) of most other eukaryotic cells, kmt in Nyctotherus completely disassemble after incubation at 6-8 degrees C (60 min) and most disappear after prolonged exposure to vinblastine (10(-5) M, 16 h). The depolymerization of kmt causes the collapse of the spindle and a dislocation of chromosomes at metaphase, yet the reduced number of kmt after vinblastine-treatment still allows an alignment of composite complexes at the spindle equator. The data suggest that three individual sets of mt exist in the interpolar spindle region during ana- and telophase: 1) interpolar mt (int mt), which are assembled during anaphase, are cold- and vinblastine sensitive; 2) manchette mt (ma mt), which are first observed underneath the nuclear envelope during mid-anaphase, are cold-stable and insensitive to vinblastine treatment (10(-5) M); after prolonged treatment (16 h) they form spiral structures; 3) stembody mt (st mt), comprising the interpolar region of the nucleus during telophase, are cold- and vinblastine insensitive. Paracrystalline structures resembling a stembody are formed in telophase-like division stages after prolonged vinblastine exposure (16 h, 10(-5) M). Since kmt and int mt possess the same sensitivity under depolymerizing conditions, they probably have a similar composition. Thus the idea that the int mt in this organism arise by elongation of kmt is supported. However, st mt apparently do not originate from an extension of preexistent int mt, but appear to represent a new set of stable mt. This is emphasized not only by their greater stability compared to the int mt but also by the distribution of cold-stable mt in late anaphase micronuclei. The ma mt may be an intermediary step in formation of st mt since their stability resembles that of the st mt. A comparison of the substructure of vinblastine-induced paracrystals in Nyctotherus with those observed in in vitro systems with known composition suggests that a turnover of MAPs may be responsible for the different stability of mt and thus could specify and regulate mt sensitivity and function. Another organelle, possibly involved in conferring stability to mt, is the nuclear membrane. The assumption that the nuclear envelope possesses an intrinsic property to nucleate mt and thus aid in the alignment of mt is supported.

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Year:  1982        PMID: 6813060     DOI: 10.1007/bf00330781

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  22 in total

1.  Cold-labile and cold-stable microtubules in the mitotic spindle of mammalian cells.

Authors:  B R Brinkley; J Cartwright
Journal:  Ann N Y Acad Sci       Date:  1975-06-30       Impact factor: 5.691

2.  Interaction of drugs with microtubule proteins.

Authors:  L Wilson; J R Bamburg; S B Mizel; L M Grisham; K M Creswell
Journal:  Fed Proc       Date:  1974-02

3.  Mitotic mechanism based on intrinsic microtubule behaviour.

Authors:  R L Margolis; L Wilson; B I Keifer
Journal:  Nature       Date:  1978-03-30       Impact factor: 49.962

4.  Tau and HMW microtubule-associated proteins have different microtubule binding sites in vivo.

Authors:  J A Connolly; V I Kalnins
Journal:  Eur J Cell Biol       Date:  1980-08       Impact factor: 4.492

5.  The structure of the cold-stable kinetochore fiber in metaphase PtK1 cells.

Authors:  C L Rieder
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

Review 6.  Substructural analysis of the microtubule and its polymorphic forms.

Authors:  K Fujiwara; L G Tilney
Journal:  Ann N Y Acad Sci       Date:  1975-06-30       Impact factor: 5.691

7.  Role of tubulin-associated proteins in microtubule nucleation and elongation.

Authors:  D B Murphy; K A Johnson; G G Borisy
Journal:  J Mol Biol       Date:  1977-11-25       Impact factor: 5.469

8.  An analysis of spindle ultrastructure during prometaphase and metaphase of micronuclear division in Tetrahymena.

Authors:  J R LaFountain; L A Davidson
Journal:  Chromosoma       Date:  1979       Impact factor: 4.316

9.  Pressure-induced depolymerization of spindle microtubules. III. Differential stability in HeLa cells.

Authors:  E D Salmon; D Goode; T K Maugel; D B Bonar
Journal:  J Cell Biol       Date:  1976-05       Impact factor: 10.539

10.  Membranes in the mitotic apparatus of barley cells.

Authors:  P K Hepler
Journal:  J Cell Biol       Date:  1980-08       Impact factor: 10.539

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  4 in total

Review 1.  Holocentromere identity: from the typical mitotic linear structure to the great plasticity of meiotic holocentromeres.

Authors:  André Marques; Andrea Pedrosa-Harand
Journal:  Chromosoma       Date:  2016-08-16       Impact factor: 4.316

2.  Stabilization of overlapping microtubules by fission yeast CLASP.

Authors:  Scott V Bratman; Fred Chang
Journal:  Dev Cell       Date:  2007-12       Impact factor: 12.270

3.  Spindle microtubule differentiation and deployment during micronuclear mitosis in Paramecium.

Authors:  J B Tucker; S A Mathews; K A Hendry; J B Mackie; D L Roche
Journal:  J Cell Biol       Date:  1985-11       Impact factor: 10.539

4.  Calmodulin-microtubule association in cultured mammalian cells.

Authors:  W J Deery; A R Means; B R Brinkley
Journal:  J Cell Biol       Date:  1984-03       Impact factor: 10.539

  4 in total

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