Literature DB >> 8937987

Structure and dynamic organization of centromeres/prekinetochores in the nucleus of mammalian cells.

D He1, B R Brinkley.   

Abstract

Although considerable research has been focused on understanding the structure and molecular organization of the centromere-kinetochore complex of mitotic chromosomes, few reports have dealt with the centromere (prekinetochore) in the interphase nucleus. In the present study, we utilized anti-centromere antibodies from the serum of patients with the autoimmune disease, scleroderma CREST (calcinosis, Raynaud's phenomenon, esophageal dismotility, sclerodactyly, telangiectasia), as probes to investigate the structure and morphogenesis of the centromere in interphase nuclei of three cell lines using laser scanning confocal microscopy and immunoelectron microscopy. Of particular interest were the chromosomes of the Indian muntjac (2n = 6 in females and 2n = 7 in males), whose large centromeres are thought to have evolved through the tandem fusion of smaller centromeres of a Chinese muntjac-like progenitor species (2n = 46). The various forms and patterns of centromeres observed in the nucleus correlated with stages in the cell cycle as determined by bromodeoxyuridine labeling and apparently represent stages in prereplication, replication and maturation. Immunoelectron microscopic studies using CREST antisera indicated that the high order structure of chromatin associated with each prekinetochore undergoes a regular unfolding-refolding cycle, displaying small bead-like subunits tandemly arranged along a linear thread of centromeric DNA, much like that reported for mitotic chromosomes. Individual centromeres/prekinetochores form a stable association with the 9-13 nm core filaments of the nucleoskeletal network in the nucleus that later become the chromosome scaffold of mitotic chromosomes. Our findings provide morphological support for the hypothesis that the spatial arrangements of individual centromeres within the nucleus may have influenced centromeric translocations and fusions during chromosome evolution. Therefore, the centromere-kinetochore complex, best known for its essential role in partitioning chromosomes in mitosis and meiosis, may also function in chromosome movements and associations in interphase.

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Year:  1996        PMID: 8937987     DOI: 10.1242/jcs.109.11.2693

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  18 in total

1.  Visualization of prekinetochore locus on the centromeric region of highly extended chromatin fibers: does kinetochore autoantigen CENP-C constitute a kinetochore organizing center?

Authors:  K Sugimoto; M Tsutsui; D AuCoin; B K Vig
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  New centromeric component CENP-W is an RNA-associated nuclear matrix protein that interacts with nucleophosmin/B23 protein.

Authors:  Younghwa Chun; Byoungwoo Park; Wansoo Koh; Sunhee Lee; Yeongmi Cheon; Raehyung Kim; Lihua Che; Soojin Lee
Journal:  J Biol Chem       Date:  2011-10-14       Impact factor: 5.157

Review 3.  Beyond the code: the mechanical properties of DNA as they relate to mitosis.

Authors:  Kerry S Bloom
Journal:  Chromosoma       Date:  2007-12-04       Impact factor: 4.316

4.  Pericentric chromatin is organized into an intramolecular loop in mitosis.

Authors:  Elaine Yeh; Julian Haase; Leocadia V Paliulis; Ajit Joglekar; Lisa Bond; David Bouck; E D Salmon; Kerry S Bloom
Journal:  Curr Biol       Date:  2008-01-22       Impact factor: 10.834

5.  Structural requirements and dynamics of mitosin-kinetochore interaction in M phase.

Authors:  X Zhu
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

6.  HCP-4, a CENP-C-like protein in Caenorhabditis elegans, is required for resolution of sister centromeres.

Authors:  L L Moore; M B Roth
Journal:  J Cell Biol       Date:  2001-06-11       Impact factor: 10.539

7.  Pericentromere clustering in Tradescantia section Rhoeo involves self-associations of AT- and GC-rich heterochromatin fractions, is developmentally regulated, and increases during differentiation.

Authors:  Hieronim Golczyk; Arleta Limanówka; Anna Uchman-Książek
Journal:  Chromosoma       Date:  2020-07-17       Impact factor: 4.316

8.  The domain structure of centromeres is conserved from fission yeast to humans.

Authors:  B Kniola; E O'Toole; J R McIntosh; B Mellone; R Allshire; S Mengarelli; K Hultenby; K Ekwall
Journal:  Mol Biol Cell       Date:  2001-09       Impact factor: 4.138

9.  HCP-4/CENP-C promotes the prophase timing of centromere resolution by enabling the centromere association of HCP-6 in Caenorhabditis elegans.

Authors:  Landon L Moore; Gerald Stanvitch; Mark B Roth; David Rosen
Journal:  Mol Cell Biol       Date:  2005-04       Impact factor: 4.272

10.  cin-4, a gene with homology to topoisomerase II, is required for centromere resolution by cohesin removal from sister kinetochores during mitosis.

Authors:  Gerald Stanvitch; Landon L Moore
Journal:  Genetics       Date:  2008-01       Impact factor: 4.562

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