Literature DB >> 3539554

Arrangements of kinetochores in mouse cells during meiosis and spermiogenesis.

B R Brinkley, S L Brenner, J M Hall, A Tousson, R D Balczon, M M Valdivia.   

Abstract

Antibodies from the serum of patients with the autoimmune disease scleroderma CREST were used to investigate the association and distribution of kinetochores in mouse cells during meiosis and spermiogenesis. The pattern of indirect immunofluorescent staining in pachytene nuclei indicated that each autosomal bivalent contains one fluorescent spot. Throughout pachytene, the kinetochores were arranged non-randomly into several clusters and distributed around the periphery of the nucleus. In subsequent stages of meiotic prophase I, distribution was random and the number of fluorescent spots increased from 21 to 40 corresponding to the diploid chromosome number and the number of halfbivalents oriented to the spindle poles at the metaphase I. Twenty pairs of kinetochores were observed at metaphase II. During spermiogenesis, the number of kinetochores correlated with the haploid chromosome number in early spermatids but tandem association of centromeres and clustering into a conspicuous chromocenter corresponded to a significant reduction in the number of fluorescent foci in mid-spermatid nuclei. The number of stained sites per nucleus continued to decrease during sperm maturation and total absence of staining was apparent in mature spermatozoa. Immunoblotting of proteins extracted from mature sperm however, indicated that a kinetochore antigen of Mr 80,000 was still present. Therefore, the absence of kinetochore staining in mature spermatozoa is probably due to the blockage of epitopes during chromatin condensation.

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Year:  1986        PMID: 3539554     DOI: 10.1007/BF00290861

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


  22 in total

1.  Preparation and spread of unfixed metaphase chromosomes for immunofluorescence staining of nuclear antigens.

Authors:  S Stenman; M Rosenqvist; N R Ringertz
Journal:  Exp Cell Res       Date:  1975-01       Impact factor: 3.905

2.  Identification and redistribution of lamins during nuclear differentiation in mouse spermatogenesis.

Authors:  G G Maul; B T French; K B Bechtol
Journal:  Dev Biol       Date:  1986-05       Impact factor: 3.582

3.  Arrangement of centromeres in mouse cells.

Authors:  T C Hsu; J E Cooper; M L Mace; B R Brinkley
Journal:  Chromosoma       Date:  1971       Impact factor: 4.316

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

Review 5.  The formation, structure, and composition of the mammalian kinetochore and kinetochore fiber.

Authors:  C L Rieder
Journal:  Int Rev Cytol       Date:  1982

6.  Different central nervous system cell types display distinct and nonrandom arrangements of satellite DNA sequences.

Authors:  L Manuelidis
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

7.  Human anticentromere antibodies: distribution, characterization of antigens, and effect on microtubule organization.

Authors:  J V Cox; E A Schenk; J B Olmsted
Journal:  Cell       Date:  1983-11       Impact factor: 41.582

8.  Autoantibody to centromere (kinetochore) in scleroderma sera.

Authors:  Y Moroi; C Peebles; M J Fritzler; J Steigerwald; E M Tan
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

9.  The CREST syndrome: a distinct serologic entity with anticentromere antibodies.

Authors:  M J Fritzler; T D Kinsella
Journal:  Am J Med       Date:  1980-10       Impact factor: 4.965

10.  Kinetochore structure, duplication, and distribution in mammalian cells: analysis by human autoantibodies from scleroderma patients.

Authors:  S Brenner; D Pepper; M W Berns; E Tan; B R Brinkley
Journal:  J Cell Biol       Date:  1981-10       Impact factor: 10.539

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  35 in total

1.  The ubiquitin ligase component Siah1a is required for completion of meiosis I in male mice.

Authors:  Ross A Dickins; Ian J Frew; Colin M House; Moira K O'Bryan; Andrew J Holloway; Izhak Haviv; Nadia Traficante; David M de Kretser; David D L Bowtell
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

2.  Principles of the highly ordered arrangement of metaphase I bivalents in spermatocytes of Agrodiaetus (Insecta, Lepidoptera).

Authors:  Vladimir A Lukhtanov; Alexander V Dantchenko
Journal:  Chromosome Res       Date:  2002       Impact factor: 5.239

3.  Cell cycle dependent chromosomal movement in pre-mitotic human T-lymphocyte nuclei.

Authors:  M Ferguson; D C Ward
Journal:  Chromosoma       Date:  1992-08       Impact factor: 4.316

Review 4.  Changing partners: moving from non-homologous to homologous centromere pairing in meiosis.

Authors:  Mara N Stewart; Dean S Dawson
Journal:  Trends Genet       Date:  2008-09-18       Impact factor: 11.639

Review 5.  Couples, pairs, and clusters: mechanisms and implications of centromere associations in meiosis.

Authors:  David Obeso; Roberto J Pezza; Dean Dawson
Journal:  Chromosoma       Date:  2013-10-15       Impact factor: 4.316

6.  A nucleolar auto-antigen is part of a major chromosomal surface component.

Authors:  Y Yasuda; G G Maul
Journal:  Chromosoma       Date:  1990-04       Impact factor: 4.316

7.  A method that allows the assembly of kinetochore components onto chromosomes condensed in clarified Xenopus egg extracts.

Authors:  A Desai; H W Deacon; C E Walczak; T J Mitchison
Journal:  Proc Natl Acad Sci U S A       Date:  1997-11-11       Impact factor: 11.205

8.  The centromere specific histone CENP-A is selectively retained in discrete foci in mammalian sperm nuclei.

Authors:  D K Palmer; K O'Day; R L Margolis
Journal:  Chromosoma       Date:  1990-12       Impact factor: 4.316

9.  Organization of the Y chromosome in testis cells of fetal, subadult and adult mice as determined by in situ hybridization.

Authors:  M Guttenbach; H Winking; M Schmid
Journal:  Chromosoma       Date:  1993-11       Impact factor: 4.316

10.  The synaptonemal complex protein Zip1 promotes bi-orientation of centromeres at meiosis I.

Authors:  Mara N Gladstone; David Obeso; Hoa Chuong; Dean S Dawson
Journal:  PLoS Genet       Date:  2009-12-11       Impact factor: 5.917

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