Literature DB >> 1613773

Chromosome in situ suppression hybridisation in human male meiosis.

A S Goldman1, M A Hultén.   

Abstract

Chromosome in situ suppression hybridisation with biotinylated whole chromosome libraries permits the unequivocable identification of specific human somatic chromosomes in numerous situations. We have now used this so called 'chromosome painting' technique in meiotically dividing cells, isolated from human testicular biopsy. It is shown that the method allows identification of target homologues, bivalents, and sister chromatids throughout the relevant stages of meiosis. Thus, a more accurate study of meiosis per se is now available to increase our understanding of such processes as first meiotic synapsis of homologues and chiasma formation/meiotic crossing over, which are still outstanding biological enigmas. The new technology also makes it possible, for the first time, (1) to obtain direct numerical data in first meiotic non-disjunction for individual chromosomes, and (2) to quantify segregation in male carriers of structural rearrangements. We exemplify the use of the chromosome painting technique for a first meiotic segregation analysis of an insertional translocation carrier.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1613773      PMCID: PMC1015847          DOI: 10.1136/jmg.29.2.98

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  21 in total

1.  Detection of aneuploidy and aneuploidy-inducing agents in human lymphocytes using fluorescence in situ hybridization with chromosome-specific DNA probes.

Authors:  D A Eastmond; D Pinkel
Journal:  Mutat Res       Date:  1990-10       Impact factor: 2.433

2.  Use of fluorescent in situ hybridization to detect chromosomal rearrangements in somatic cell hybrids.

Authors:  A J Giaccia; J W Evans; J M Brown
Journal:  Genes Chromosomes Cancer       Date:  1990-09       Impact factor: 5.006

3.  Fluorescence in situ hybridization to Y chromosomes in decondensed human sperm nuclei.

Authors:  A J Wyrobek; T Alhborn; R Balhorn; L Stanker; D Pinkel
Journal:  Mol Reprod Dev       Date:  1990-11       Impact factor: 2.609

4.  Labeling of human centromeres using an alphoid DNA consensus sequence: application to the scoring of chromosome aberrations.

Authors:  J Meyne; L G Littlefield; R K Moyzis
Journal:  Mutat Res       Date:  1989-06       Impact factor: 2.433

5.  Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization.

Authors:  B Trask; G van den Engh; D Pinkel; J Mullikin; F Waldman; H van Dekken; J Gray
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

6.  A new application of in situ hybridization: detection of numerical and structural chromosome aberrations with a combination centromeric-telomeric DNA probe.

Authors:  H van Dekken; J G Bauman
Journal:  Cytogenet Cell Genet       Date:  1988

7.  Rapid interphase and metaphase assessment of specific chromosomal changes in neuroectodermal tumor cells by in situ hybridization with chemically modified DNA probes.

Authors:  T Cremer; D Tesin; A H Hopman; L Manuelidis
Journal:  Exp Cell Res       Date:  1988-06       Impact factor: 3.905

8.  Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Authors:  D Pinkel; J Landegent; C Collins; J Fuscoe; R Segraves; J Lucas; J Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

9.  Reproducible compartmentalization of individual chromosome domains in human CNS cells revealed by in situ hybridization and three-dimensional reconstruction.

Authors:  L Manuelidis; J Borden
Journal:  Chromosoma       Date:  1988       Impact factor: 4.316

10.  Three-dimensional analysis of the organization of human chromosome domains in human and human-hamster hybrid interphase nuclei.

Authors:  H van Dekken; D Pinkel; J Mullikin; B Trask; G van den Engh; J Gray
Journal:  J Cell Sci       Date:  1989-10       Impact factor: 5.285

View more
  9 in total

1.  Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

Authors:  S J Armstrong; A S Goldman; R M Speed; M A Hultén
Journal:  Am J Hum Genet       Date:  2000-08-08       Impact factor: 11.025

Review 2.  Demystified ... FISH.

Authors:  J J Waters; A L Barlow; C P Gould
Journal:  Mol Pathol       Date:  1998-04

3.  Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm.

Authors:  P Van Hummelen; D Manchester; X Lowe; A J Wyrobek
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

4.  Combined immunocytogenetic and molecular cytogenetic analysis of meiosis I human spermatocytes.

Authors:  A L Barlow; M A Hultén
Journal:  Chromosome Res       Date:  1996-12       Impact factor: 5.239

5.  A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis.

Authors:  Y E Cheng; S M Gartler
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

6.  On the origin of crossover interference: A chromosome oscillatory movement (COM) model.

Authors:  Maj A Hultén
Journal:  Mol Cytogenet       Date:  2011-04-08       Impact factor: 2.009

7.  Meiotic chromosome condensation and pairing in Saccharomyces cerevisiae studied by chromosome painting.

Authors:  H Scherthan; J Loidl; T Schuster; D Schweizer
Journal:  Chromosoma       Date:  1992-10       Impact factor: 4.316

8.  XY chromosome behaviour in the germ-line of the human male: a FISH analysis of spatial orientation, chromatin condensation and pairing.

Authors:  S J Armstrong; A J Kirkham; M A Hultén
Journal:  Chromosome Res       Date:  1994-11       Impact factor: 5.239

9.  Chromosome painting reveals asynaptic full alignment of homologs and HIM-8-dependent remodeling of X chromosome territories during Caenorhabditis elegans meiosis.

Authors:  Kentaro Nabeshima; Susanna Mlynarczyk-Evans; Anne M Villeneuve
Journal:  PLoS Genet       Date:  2011-08-18       Impact factor: 5.917

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.