Literature DB >> 2578344

Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis.

M Lalande, R R Schreck, R Hoffman, S A Latt.   

Abstract

A dual laser FACS IV cell sorter has been used to obtain bivariate flow histograms of human metaphase chromosomes stained with the DNA-specific dyes, 33258 Hoechst and chromomycin A3. Approximately twenty distinct chromosomal fluorescence populations can be resolved using this double staining technique and the flow cytometer which has been modified only by the substitution of a specially designed air-spaced achromat for the standard focusing lens. Metaphase chromosomes from two different cell lines bearing inverted duplicated #15 autosomes have been subjected to bivariate chromosome analysis. In both cases, the inverted duplicated #15 chromosomes have been identified in the bivariate flow histogram. This identification was supported by experiments in which doubly stained chromosomes were counterstained with either netropsin or distamycin A, resulting in a relative increase in the 33258 Hoechst fluorescence intensity of the structurally abnormal #15 chromosomes, compared with the other chromosomes, as predicted by cytological studies. The possibility of identifying and separating small abnormal autosomes using commercially available instrumentation should facilitate the use of recombinant DNA techniques for the construction of libraries which are highly enriched for DNA sequences from limited autosomal subregions important in the study of chromosomal abnormalities such as deletions, translocations and inversion duplications.

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Year:  1985        PMID: 2578344     DOI: 10.1002/cyto.990060102

Source DB:  PubMed          Journal:  Cytometry        ISSN: 0196-4763


  7 in total

1.  The binding kinetics and interaction of DNA fluorochromes used in the analysis of nuclei and chromosomes by flow cytometry.

Authors:  G J van den Engh; B J Trask; J W Gray
Journal:  Histochemistry       Date:  1986

2.  Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes.

Authors:  U Tantravahi; G D Stewart; M Van Keuren; G McNeil; S Roy; D Patterson; H Drabkin; M Lalande; D M Kurnit; S A Latt
Journal:  Hum Genet       Date:  1988-07       Impact factor: 4.132

3.  Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.

Authors:  P Harris; M Lalande; H Stroh; G Bruns; A Flint; S A Latt
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

4.  Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes.

Authors:  T A Donlon
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

5.  Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.

Authors:  J Wagstaff; J H Knoll; J Fleming; E F Kirkness; A Martin-Gallardo; F Greenberg; J M Graham; J Menninger; D Ward; J C Venter
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

6.  Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.

Authors:  T A Donlon; M Lalande; A Wyman; G Bruns; S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

7.  Moderately repeated DNA sequences specific for the short arm of the human Y chromosome are present in XX males and reduced in copy number in an XY female.

Authors:  U Müller; M Lalande; T Donlon; S A Latt
Journal:  Nucleic Acids Res       Date:  1986-02-11       Impact factor: 16.971

  7 in total

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