Literature DB >> 2182292

Human gametes and zygotes studied by nonradioactive in situ hybridization.

M H Pieters1, J P Geraedts, H Meyer, J C Dumoulin, J L Evers, R J Jongbloed, P M Nederlof, S van der Flier.   

Abstract

A nonradioactive in situ hybridization technique was applied to human gametes and abnormally fertilized or developed zygotes. Using haptenized chromosome-specific probes, visualization was obtained using immunocytochemistry to achieve a fluorescent stain on specific hybrids. Using a chromosome 1-specific DNA probe, almost all spermatozoa gave a positive result, i.e., one hybridization signal per cell could be observed. Furthermore, it was possible to identify sperm cells with two spots, suggesting nondisjunction. Two cleavage arrested embryos from different patients showed both: two brightly fluorescent spots and two weaker spots with the same DNA probe. Using a Y-specific DNA probe the percentages of positive spermatozoa from the normal males ranged between 48.1% and 49.1%. In an embryo with four grossly haploid chromosome sets, three fluorescent spots were obtained with the Y-specific DNA probe, indicating the penetration of three spermatozoa.

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Year:  1990        PMID: 2182292     DOI: 10.1159/000132886

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  15 in total

1.  Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei.

Authors:  M Guttenbach; M Schmid
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

2.  Reduction in signal overlap results in increased FISH efficiency: implications for preimplantation genetic diagnosis.

Authors:  S Munné; T Dailey; M Finkelstein; H U Weier
Journal:  J Assist Reprod Genet       Date:  1996-02       Impact factor: 3.412

3.  Fluorescence in situ hybridization with chromosome paint probes: a novel approach to assess aneuploidy in human sperm nuclei.

Authors:  N Rives; S Wust; B David; V Duchesne; G Joly; B Mace
Journal:  J Assist Reprod Genet       Date:  1999-01       Impact factor: 3.412

4.  Rapid chromosome detection in human gametes, zygotes, and preimplantation embryos using the PRINS technique.

Authors:  F Pellestor; A Girardet; G Lefort; B Andréo; J P Charlieu
Journal:  J Assist Reprod Genet       Date:  1996-09       Impact factor: 3.412

5.  Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization.

Authors:  M Guttenbach; R Schakowski; M Schmid
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

6.  Aneuploidy in spermatozoa using fluorescence in situ hybridization.

Authors:  G L Schattman; S Munné; J G Grifo; L Carton; J Cohen
Journal:  J Assist Reprod Genet       Date:  1993-07       Impact factor: 3.412

7.  Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradioactive in situ hybridization.

Authors:  M Guttenbach; R Schakowski; M Schmid
Journal:  Hum Genet       Date:  1994-01       Impact factor: 4.132

8.  Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization.

Authors:  N Miharu; R G Best; S R Young
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132

9.  Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y.

Authors:  W A Robbins; R Segraves; D Pinkel; A J Wyrobek
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

10.  Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridization.

Authors:  J M Holmes; R H Martin
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

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