Literature DB >> 3383699

Sequence of centromere separation: generation of unstable multicentric chromosomes in a rat cell line.

B K Vig1, N Paweletz.   

Abstract

A transformed cell line, B1, of cerebral endothelial origin from the Wistar-Kyoto male rat has chromatid and chromosome type bridges in virtually every cell. It exhibits various dicentric and polycentric chromosomes. Most dicentrics are symmetric isochromosomes. Certain isodicentrics are present in a fair segment of the cell population; however, almost all cells have some newly arising isodicentrics. The live cells show a lengthened prometaphase. Anaphase is also retarded possibly due to the occurrence of bridges. At anaphase some multicentrics split at only one centromere. When pulled to the two poles the unsplit centromeres and the distal chromosome segment form a side arm bridge. Another mechanism appears to be a total lack of separation of daughter centromeres at meta-anaphase ('meiotic-like' behavior of mitotic chromosomes). This is realized by the pulling of each of the two unsplit centromeres to opposite poles and results in bridges with both sister chromatids running parallel to each other. A break at corresponding weak points in the two sister chromatids followed by rejoining can form a dicentric isochromosome. A third mechanism, the breakage-fusion-bridge cycle, is also operative but would not produce isodicentrics. In the case of the first two mechanisms some or all centromeres apparently split between telophase and onset of the following DNA synthesis rather than at the usual time at late metaphase. These observations may suggest some previously unknown behavior of multicentric chromosomes during mitosis.

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Year:  1988        PMID: 3383699     DOI: 10.1007/bf00286914

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


  11 in total

1.  Telomeric association in two human renal tumors.

Authors:  G Kovacs; R Müller-Brechlin; S Szücs
Journal:  Cancer Genet Cytogenet       Date:  1987-10

2.  Sequence of centromere separation: a mechanism for orderly separation of dicentrics.

Authors:  B K Vig; R P Zinkowski
Journal:  Cancer Genet Cytogenet       Date:  1986-08

3.  A low-viscosity epoxy resin embedding medium for electron microscopy.

Authors:  A R Spurr
Journal:  J Ultrastruct Res       Date:  1969-01

4.  Characterization of kinetochores in multicentric chromosomes.

Authors:  R P Zinkowski; B K Vig; D Broccoli
Journal:  Chromosoma       Date:  1986       Impact factor: 4.316

5.  Anti-kinetochore antibodies: use as probes for inactive centromeres.

Authors:  D E Merry; S Pathak; T C Hsu; B R Brinkley
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

6.  Three related centromere proteins are absent from the inactive centromere of a stable isodicentric chromosome.

Authors:  W C Earnshaw; B R Migeon
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

7.  Karyotype evolution in a transformed rat cerebral endothelial cell line.

Authors:  M Tyrkus; C A Diglio; N Gohle
Journal:  Int J Cancer       Date:  1983-10-15       Impact factor: 7.396

8.  Sequence of centromere separation: orderly separation of multicentric chromosomes in mouse L cells.

Authors:  B K Vig
Journal:  Chromosoma       Date:  1984       Impact factor: 4.316

9.  Membranes in the mitotic apparatus of barley cells.

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

10.  Transformation of rat cerebral endothelial cells by Rous sarcoma virus.

Authors:  C A Diglio; D E Wolfe; P Meyers
Journal:  J Cell Biol       Date:  1983-07       Impact factor: 10.539

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  2 in total

1.  Visualization of centromere proteins CENP-B and CENP-C on a stable dicentric chromosome in cytological spreads.

Authors:  W C Earnshaw; H Ratrie; G Stetten
Journal:  Chromosoma       Date:  1989-06       Impact factor: 4.316

2.  Sequence of centromere separation: characterization of multicentric chromosomes in a rat cell line.

Authors:  D Broccoli; N Paweletz; B K Vig
Journal:  Chromosoma       Date:  1989-06       Impact factor: 4.316

  2 in total

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