Rapid identification of marker chromosomes by in situ hybridization under different stringency conditions. 1994

S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
Institute of Pediatrics and Childrens Surgery, MH RF, Moscow, Russia.

Six metacentric non-satellite chromosome markers and 4 satellite markers of unknown origin were discovered by routine cytogenetic analysis. These markers were then investigated by isotopic and nonisotopic (FISH) in situ hybridization. In order to determine the origin of small marker chromosomes, a special protocol involving sequential application of defined alphoid and 'classical' satellite DNA probes with chromosome specificity was used. In situ hybridization under low stringency conditions has been performed with DNA probes specific for 4 groups of chromosomes. After preliminary analysis and determination of the possible origin of these marker chromosomes, DNA probes with high chromosome specificity were used under high stringency conditions. Marker chromosomes were found to be derivatives of chromosomes 7, 9 (3 cases), 13, 14 or 22, 21 (2 cases), X and Y.

UI MeSH Term Description Entries
D007621 Karyotyping Mapping of the KARYOTYPE of a cell. Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D002877 Chromosomes, Human Very long DNA molecules and associated proteins, HISTONES, and non-histone chromosomal proteins (CHROMOSOMAL PROTEINS, NON-HISTONE). Normally 46 chromosomes, including two sex chromosomes are found in the nucleus of human cells. They carry the hereditary information of the individual. Chromosome, Human,Human Chromosome,Human Chromosomes
D004276 DNA, Satellite Highly repetitive DNA sequences found in HETEROCHROMATIN, mainly near centromeres. They are composed of simple sequences (very short) (see MINISATELLITE REPEATS) repeated in tandem many times to form large blocks of sequence. Additionally, following the accumulation of mutations, these blocks of repeats have been repeated in tandem themselves. The degree of repetition is on the order of 1000 to 10 million at each locus. Loci are few, usually one or two per chromosome. They were called satellites since in density gradients, they often sediment as distinct, satellite bands separate from the bulk of genomic DNA owing to a distinct BASE COMPOSITION. Satellite DNA,Satellite I DNA,DNA, Satellite I,DNAs, Satellite,DNAs, Satellite I,I DNA, Satellite,I DNAs, Satellite,Satellite DNAs,Satellite I DNAs
D005819 Genetic Markers A phenotypically recognizable genetic trait which can be used to identify a genetic locus, a linkage group, or a recombination event. Chromosome Markers,DNA Markers,Markers, DNA,Markers, Genetic,Genetic Marker,Marker, Genetic,Chromosome Marker,DNA Marker,Marker, Chromosome,Marker, DNA,Markers, Chromosome
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor
D015342 DNA Probes Species- or subspecies-specific DNA (including COMPLEMENTARY DNA; conserved genes, whole chromosomes, or whole genomes) used in hybridization studies in order to identify microorganisms, to measure DNA-DNA homologies, to group subspecies, etc. The DNA probe hybridizes with a specific mRNA, if present. Conventional techniques used for testing for the hybridization product include dot blot assays, Southern blot assays, and DNA:RNA hybrid-specific antibody tests. Conventional labels for the DNA probe include the radioisotope labels 32P and 125I and the chemical label biotin. The use of DNA probes provides a specific, sensitive, rapid, and inexpensive replacement for cell culture techniques for diagnosing infections. Chromosomal Probes,DNA Hybridization Probe,DNA Probe,Gene Probes, DNA,Conserved Gene Probes,DNA Hybridization Probes,Whole Chromosomal Probes,Whole Genomic DNA Probes,Chromosomal Probes, Whole,DNA Gene Probes,Gene Probes, Conserved,Hybridization Probe, DNA,Hybridization Probes, DNA,Probe, DNA,Probe, DNA Hybridization,Probes, Chromosomal,Probes, Conserved Gene,Probes, DNA,Probes, DNA Gene,Probes, DNA Hybridization,Probes, Whole Chromosomal
D017404 In Situ Hybridization, Fluorescence A type of IN SITU HYBRIDIZATION in which target sequences are stained with fluorescent dye so their location and size can be determined using fluorescence microscopy. This staining is sufficiently distinct that the hybridization signal can be seen both in metaphase spreads and in interphase nuclei. FISH Technique,Fluorescent in Situ Hybridization,Hybridization in Situ, Fluorescence,FISH Technic,Hybridization in Situ, Fluorescent,In Situ Hybridization, Fluorescent,FISH Technics,FISH Techniques,Technic, FISH,Technics, FISH,Technique, FISH,Techniques, FISH

Related Publications

S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
January 1995, Urologia internationalis,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
January 1998, Annales de genetique,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
January 1993, Hematological oncology,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
August 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
August 1997, American journal of medical genetics,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
August 1994, Trends in genetics : TIG,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
July 1994, Prenatal diagnosis,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
January 2016, Molecular cytogenetics,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
August 2001, Human genetics,
S G Vorsanova, and Y B Yurov, and I V Soloviev, and I A Demidova, and P Malet
August 1993, American journal of human genetics,
Copied contents to your clipboard!