Literature DB >> 15750029

An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.

Ivan Y Iourov1, Ilia V Soloviev, Svetlana G Vorsanova, Viktor V Monakhov, Yuri B Yurov.   

Abstract

A number of applied molecular cytogenetic studies require the quantitative assessment of fluorescence in situ hybridization (FISH) signals (for example, interphase FISH analysis of aneuploidy by chromosome enumeration DNA probes; analysis of somatic pairing of homologous chromosomes in interphase nuclei; identification of chromosomal heteromorphism after FISH with satellite DNA probes for differentiation of parental origin of homologous chromosome, etc.). We have performed a pilot study to develop a simple technique for quantitative assessment of FISH signals by means of the digital capturing of microscopic images and the intensity measuring of hybridization signals using Scion Image software, commonly used for quantification of electrophoresis gels. We have tested this approach by quantitative analysis of FISH signals after application of chromosome-specific DNA probes for aneuploidy scoring in interphase nuclei in cells of different human tissues. This approach allowed us to exclude or confirm a low-level mosaic form of aneuploidy by quantification of FISH signals (for example, discrimination of pseudo-monosomy and artifact signals due to over-position of hybridization signals). Quantification of FISH signals was also used for analysis of somatic pairing of homologous chromosomes in nuclei of postmortem brain tissues after FISH with "classical" satellite DNA probes for chromosomes 1, 9, and 16. This approach has shown a relatively high efficiency for the quantitative registration of chromosomal heteromorphism due to variations of centromeric alphoid DNA in homologous parental chromosomes. We propose this approach to be efficient and to be considered as a useful tool in addition to visual FISH signal analysis for applied molecular cytogenetic studies.

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Year:  2005        PMID: 15750029     DOI: 10.1369/jhc.4A6419.2005

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  19 in total

1.  On the paternal origin of trisomy 21 Down syndrome.

Authors:  Maj A Hultén; Suketu D Patel; Magnus Westgren; Nikos Papadogiannakis; Anna Maria Jonsson; Jon Jonasson; Erik Iwarsson
Journal:  Mol Cytogenet       Date:  2010-02-23       Impact factor: 2.009

2.  Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB).

Authors:  I Y Iourov; T Liehr; S G Vorsanova; A D Kolotii; Y B Yurov
Journal:  Chromosome Res       Date:  2006-04-20       Impact factor: 5.239

3.  Analysis of HER2 gene amplification using an automated fluorescence in situ hybridization signal enumeration system.

Authors:  Rachel Stevens; Imad Almanaseer; Miguel Gonzalez; Derin Caglar; Ryan A Knudson; Rhett P Ketterling; Daniel S Schrock; Thomas A Seemayer; Julia A Bridge
Journal:  J Mol Diagn       Date:  2007-04       Impact factor: 5.568

4.  Quantitative analysis of centromeric FISH spots during the cell cycle by image cytometry.

Authors:  Genta Amakawa; Kenzo Ikemoto; Hideaki Ito; Tomoko Furuya; Kohsuke Sasaki
Journal:  J Histochem Cytochem       Date:  2013-07-04       Impact factor: 2.479

5.  Human interphase chromosomes: a review of available molecular cytogenetic technologies.

Authors:  Svetlana G Vorsanova; Yuri B Yurov; Ivan Y Iourov
Journal:  Mol Cytogenet       Date:  2010-01-11       Impact factor: 2.009

6.  Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: a search for familial genetic markers for autistic disorders.

Authors:  S G Vorsanova; V Yu Voinova; I Yu Yurov; O S Kurinnaya; I A Demidova; Yu B Yurov
Journal:  Neurosci Behav Physiol       Date:  2010-09

7.  Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders.

Authors:  S G Vorsanova; I Yu Yurov; I A Demidova; V Yu Voinova-Ulas; V S Kravets; I V Solov'ev; N L Gorbachevskaya; Yu B Yurov
Journal:  Neurosci Behav Physiol       Date:  2007-07

Review 8.  The genomically mosaic brain: aneuploidy and more in neural diversity and disease.

Authors:  Diane M Bushman; Jerold Chun
Journal:  Semin Cell Dev Biol       Date:  2013-03-04       Impact factor: 7.727

9.  Germinal and Somatic Trisomy 21 Mosaicism: How Common is it, What are the Implications for Individual Carriers and How Does it Come About?

Authors:  Maj A Hultén; Jon Jonasson; Ann Nordgren; Erik Iwarsson
Journal:  Curr Genomics       Date:  2010-09       Impact factor: 2.236

10.  Molecular cytogenetic diagnosis and somatic genome variations.

Authors:  S G Vorsanova; Y B Yurov; I V Soloviev; I Y Iourov
Journal:  Curr Genomics       Date:  2010-09       Impact factor: 2.236

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