Literature DB >> 12906132

Pericentromeric euchromatin is conserved in minute human supernumerary chromosomes: a study using cross-species colour segmenting (RxFISH).

Louise V Hills1, Sara Nouri, Howard R Slater.   

Abstract

Investigation of marker chromosomes is one of the most challenging areas of clinical cytogenetics, especially in the prenatal scenario. A range of techniques including microdissection/reverse painting, SKY and M-FISH are available for the investigation of larger markers (>3 Mb). All these techniques rely on hybridization of unique, homologous sequences with simultaneous suppression of repeat sequences. In contrast, RxFISH is based on hybridization of cross-species syntenic sequences; repeat sequences do not hybridize due to species divergence. We have used RxFISH to analyse a group of the smallest, i.e. minute, supernumerary marker chromosomes. Our results suggest that even the smallest marker chromosomes often contain conserved pericentric euchromatin. More detailed characterization of pericentric genetic content is needed to assess the clinical significance of minute supernumerary markers.

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Year:  2003        PMID: 12906132     DOI: 10.1023/a:1024096024847

Source DB:  PubMed          Journal:  Chromosome Res        ISSN: 0967-3849            Impact factor:   5.239


  11 in total

1.  Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.

Authors:  M B Delatycki; L Voullaire; D Francis; V Petrovic; A Robertson; L M Webber; H R Slater
Journal:  J Med Genet       Date:  1999-04       Impact factor: 6.318

Review 2.  Lessons from the human genome: transitions between euchromatin and heterochromatin.

Authors:  J E Horvath; J A Bailey; D P Locke; E E Eichler
Journal:  Hum Mol Genet       Date:  2001-10-01       Impact factor: 6.150

3.  Genomic and genetic definition of a functional human centromere.

Authors:  M G Schueler; A W Higgins; M K Rudd; K Gustashaw; H F Willard
Journal:  Science       Date:  2001-10-05       Impact factor: 47.728

4.  Karyotyping human chromosomes by combinatorial multi-fluor FISH.

Authors:  M R Speicher; S Gwyn Ballard; D C Ward
Journal:  Nat Genet       Date:  1996-04       Impact factor: 38.330

5.  Multicolor spectral karyotyping of human chromosomes.

Authors:  E Schröck; S du Manoir; T Veldman; B Schoell; J Wienberg; M A Ferguson-Smith; Y Ning; D H Ledbetter; I Bar-Am; D Soenksen; Y Garini; T Ried
Journal:  Science       Date:  1996-07-26       Impact factor: 47.728

Review 6.  Position effects and genetic disease.

Authors:  E Milot; P Fraser; F Grosveld
Journal:  Trends Genet       Date:  1996-04       Impact factor: 11.639

7.  Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres.

Authors:  S J Knight; S W Horsley; R Regan; N M Lawrie; E J Maher; D L Cardy; J Flint; L Kearney
Journal:  Eur J Hum Genet       Date:  1997 Jan-Feb       Impact factor: 4.246

8.  Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations.

Authors:  M S Jackson; M Rocchi; G Thompson; T Hearn; M Crosier; J Guy; D Kirk; L Mulligan; A Ricco; S Piccininni; R Marzella; L Viggiano; N Archidiacono
Journal:  Hum Mol Genet       Date:  1999-02       Impact factor: 6.150

9.  Cross-species colour segmenting: a novel tool in human karyotype analysis.

Authors:  S Müller; P C O'Brien; M A Ferguson-Smith; J Wienberg
Journal:  Cytometry       Date:  1998-12-01

Review 10.  Neocentromeres: role in human disease, evolution, and centromere study.

Authors:  David J Amor; K H Andy Choo
Journal:  Am J Hum Genet       Date:  2002-08-26       Impact factor: 11.025

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  1 in total

1.  Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).

Authors:  T Liehr; G Hickmann; P Kozlowski; U Claussen; H Starke
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

  1 in total

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