Literature DB >> 1577461

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

H X Deng1, K Yoshiura, R W Dirks, N Harada, T Hirota, K Tsukamoto, Y Jinno, N Niikawa.   

Abstract

We describe a chromosome-band-specific painting method that involves (1) microdissection of the chromosome, chromosomal region or band, (2) amplification of a variety of chromosome/region/band-specific DNA fragments with the polymerase chain reaction (PCR), and (3) chromosome in situ suppression hybridization (CISS) with the direct use of the PCR products as a probe pool. With this method, it was possible 1) to paint an entire X or Y chromosome, a distal one-fourth of 2q, and only a band at 8q24.1, 2) to identify the origin of a minute marker chromosome in a mentally retarded patient, 3) to detect an X;Y translocation in another patient, and 4) to identify one human chromosome 2 in a human-mouse hybrid cell line. This method allows us to identify not only structural chromosome abnormalities at the band level, but also the origin of cytogenetically unidentifiable marker chromosomes. It will also be useful in studies of evolutionary cytogenetics.

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Year:  1992        PMID: 1577461     DOI: 10.1007/bf00207034

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


  17 in total

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

Authors:  F T Kao; J W Yu
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-01       Impact factor: 11.205

2.  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

3.  Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries.

Authors:  P Lichter; T Cremer; J Borden; L Manuelidis; D C Ward
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

4.  Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes.

Authors:  T Cremer; P Lichter; J Borden; D C Ward; L Manuelidis
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

5.  Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Authors:  D Pinkel; J Landegent; C Collins; J Fuscoe; R Segraves; J Lucas; J Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

6.  Construction and characterization of band-specific DNA libraries.

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

7.  Painting of human chromosomes with probes generated from hybrid cell lines by PCR with Alu and L1 primers.

Authors:  C Lengauer; H Riethman; T Cremer
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

8.  Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridization.

Authors:  P M Nederlof; S van der Flier; A K Raap; H J Tanke; M van der Ploeg; F Kornips; J P Geraedts
Journal:  Cancer Genet Cytogenet       Date:  1989-10-01

9.  Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences.

Authors:  P M Nederlof; D Robinson; R Abuknesha; J Wiegant; A H Hopman; H J Tanke; A K Raap
Journal:  Cytometry       Date:  1989-01

10.  Construction of mouse A9 clones containing a single human chromosome tagged with neomycin-resistance gene via microcell fusion.

Authors:  M Koi; M Shimizu; H Morita; H Yamada; M Oshimura
Journal:  Jpn J Cancer Res       Date:  1989-05
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  17 in total

Review 1.  Reverse painting highlights the origin of chromosome aberrations.

Authors:  Elisabeth Blennow
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

Review 2.  A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q.

Authors:  T Cai; D A Tagle; X Xia; P Yu; X X He; L Y Li; J H Xia
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

3.  The development of chromosome microdissection and microcloning technique and its applications in genomic research.

Authors:  Ruo-Nan Zhou; Zan-Min Hu
Journal:  Curr Genomics       Date:  2007-03       Impact factor: 2.236

4.  Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.

Authors:  S R Ghaffari; E Boyd; J M Connor; A M Jones; J L Tolmie
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

5.  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
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

6.  Generation of chromosome fragment specific bovine DNA sequences by microdissection and DOP-PCR.

Authors:  T Goldammer; R Weikard; R M Brunner; M Schwerin
Journal:  Mamm Genome       Date:  1996-04       Impact factor: 2.957

7.  A simple and efficient method for microdissection and microFISH.

Authors:  J J Engelen; J C Albrechts; G J Hamers; J P Geraedts
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

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

Authors:  T Ohta; T Tohma; H Soejima; Y Fukushima; T Nagai; K Yoshiura; Y Jinno; N Niikawa
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

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

Authors:  H Ohashi; K Wakui; K Ogawa; T Okano; N Niikawa; Y Fukushima
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

10.  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

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