Literature DB >> 8365720

The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

T Ohta1, T Tohma, H Soejima, Y Fukushima, T Nagai, K Yoshiura, Y Jinno, N Niikawa.   

Abstract

De novo chromosome structural abnormalities cannot always be diagnosed by the use of standard cytogenetic techniques. We applied a previously developed chromosome-band-specific painting method to the diagnosis of such rearrangements. The diagnostic procedures consisted of microdissection of an aberrant chromosomal region of a given patient, polymerase chain reaction (PCR) amplification of the dissected chromosomal DNA, and subsequent competitive fluorescence in situ hybridization (FISH) using the PCR products as a probe pool on metaphase chromosomes from the patient and/or a karyotypically normal person. With this strategy, we studied 6 de novo rearrangements (6p+, 6q+, 9p+, 17p+, +mar, and +mar) in 6 patients. These rearrangements had been seen by conventional banding but their origin could not be identified. In all 6 patients, we successfully ascertained the origin. Using an aberrant region-specific probe pool, FISH signals appeared on both the aberrant region and a region of another specific chromosome pair. A reverse probe pool that was generated through the microdissection of normal chromosomes at a candidate region for the origin of the aberration hybridized with both the aberrant and the candidate regions. We thus diagnosed one patient with 17p+ as having trisomy for 14q32-qter, one with 9p+ as having trisomy for 12pter-p12, one with 6q+ as having a tandem duplication (trisomy) of a 6q23-q25 segment, one with 6p+ as having a tandem duplication (trisomy) of a 6p23-q21.3 segment, one with a supernumerary metacentric marker chromosome as having tetrasomy for 18pter-cen, and the last with an additional small marker chromosome as having trisomy for 18p11.1 (or p11.2)-q11.2. The present targeted chromosome-band-painting method provides the simple and rapid preparation of a probe pool for region-specific FISH, and is useful for the diagnosis of chromosome abnormalities of unknown origin.

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Year:  1993        PMID: 8365720     DOI: 10.1007/bf00216136

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  24 in total

1.  Chromosome microdissection and cloning in human genome and genetic disease analysis.

Authors:  F T Kao; J W Yu
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3.  Isolation of region-specific cosmids from chromosome 5 by hybridization with microdissection clones.

Authors:  D L Saltman; G M Dolganov; B S Pearce; S S Kuo; P J Callahan; M L Cleary; M Lovett
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4.  Laser microdissection of the fragile X region: identification of cosmid clones and of conserved sequences in this region.

Authors:  M Djabali; C Nguyen; I Biunno; B A Oostra; M G Mattei; J E Ikeda; B R Jordan
Journal:  Genomics       Date:  1991-08       Impact factor: 5.736

5.  Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization.

Authors:  T Cremer; S Popp; P Emmerich; P Lichter; C Cremer
Journal:  Cytometry       Date:  1990

6.  Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.

Authors:  H X Deng; K Yoshiura; R W Dirks; N Harada; T Hirota; K Tsukamoto; Y Jinno; N Niikawa
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

7.  Microdissection of banded human chromosomes.

Authors:  G Senger; H J Lüdecke; B Horsthemke; U Claussen
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

8.  Microdissection of human chromosomal regions 8q23.3-q24.11 and 2q33-qter: construction of DNA libraries and isolation of their clones.

Authors:  T Hirota; K Tsukamoto; H X Deng; K Yoshiura; T Ohta; T Tohma; T Kibe; N Harada; Y Jinno; N Niikawa
Journal:  Genomics       Date:  1992-06       Impact factor: 5.736

9.  Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.

Authors:  A T Tharapel; M B Qumsiyeh; P R Martens; S A Tharapel; J D Dalton; J C Ward; R S Wilroy
Journal:  Am J Med Genet       Date:  1991-07-01

10.  Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probe.

Authors:  U Trautmann; G Leuteritz; G Senger; U Claussen; W G Ballhausen
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

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2.  Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH.

Authors:  J J Engelen; W J Loots; J C Albrechts; P C Motoh; J P Fryns; A J Hamers; J P Geraedts
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3.  Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique.

Authors:  C Mackie-Ogilvie; K Waddle; J Mandeville; M J Seller; Z Docherty
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

4.  Familial complex chromosome rearrangement ascertained by in situ hybridisation.

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5.  A 3 1/2 year old girl with distal trisomy 19q defined by FISH.

Authors:  C James; A Jauch; L Robson; N Watson; A Smith
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6.  Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis.

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Journal:  Am J Med Genet A       Date:  2010-07       Impact factor: 2.802

7.  A stable acentric marker chromosome: possible existence of an intercalary ancient centromere at distal 8p.

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8.  Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis.

Authors:  J Müller-Navia; A Nebel; E Schleiermacher
Journal:  Hum Genet       Date:  1995-12       Impact factor: 4.132

9.  Identification of the origin of double minutes in normal human cells by laser-based chromosome microdissection approach.

Authors:  E Rajcan-Separovic; H S Wang; M D Speevak; L Janes; R G Korneluk; K Wakasa; J E Ikeda
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

10.  De Novo Subtelomeric 6p25.3 Deletion with Duplication of 6q23.3-q27: Genotype-Phenotype Correlation.

Authors:  Emine Ikbal Atli; Hakan Gurkan; Engin Atli; Ulfet Vatansever; Betul Acunas; Cisem Mail
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