Literature DB >> 1568226

Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.

C Lengauer1, H C Riethman, M R Speicher, M Taniwaki, D Konecki, E D Green, R Becher, M V Olson, T Cremer.   

Abstract

A human yeast artificial chromosome (YAC) library was screened by polymerase chain reaction with oligonucleotide primers defined for DNA sequences of the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2. Alu-PCR-generated human DNA sequences were obtained from the respective YAC clones and used for fluorescence in situ hybridization experiments under suppression conditions. After chromosomal in situ suppression hybridization to GTG-banded human prometaphase chromosomes, seven of nine initially isolated YAC clones yielded strong signals exclusively in the chromosome bands containing the respective genes. Two clones yielded additional signals on other chromosomes and were excluded from further tests. The band-specific YACs were successfully applied to visualize specific structural chromosome aberrations in peripheral blood cells from patients with myelodysplasia exhibiting del(5)(q13q34), chronic myeloid leukemia and acute lymphocytic leukemia with t(9;22)(q34;q11), acute promyelocytic leukemia (M3) with t(15;17)(q22;q21), and in a cell line established from a proband with the constitutional translocation t(3;8)(p14.2;q24). In addition to the analysis of metaphase spreads, we demonstrate the particular usefulness of these YAC clones in combination with whole chromosome painting to analyze specific chromosome aberrations directly in the interphase nucleus.

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Mesh:

Year:  1992        PMID: 1568226

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  17 in total

Review 1.  Monitoring the course of chronic myelogenous leukemia by fluorescence in situ hybridization.

Authors:  Chu-Myong Seong
Journal:  Int J Hematol       Date:  2002-08       Impact factor: 2.490

2.  Multicolor deconvolution microscopy of thick biological specimens.

Authors:  Christine Maierhofer; Rainer Gangnus; Joachim Diebold; Michael R Speicher
Journal:  Am J Pathol       Date:  2003-02       Impact factor: 4.307

3.  Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer.

Authors:  S F Huang; S Xiao; A A Renshaw; K R Loughlin; T J Hudson; J A Fletcher
Journal:  Am J Pathol       Date:  1996-11       Impact factor: 4.307

4.  Subtracted, unique-sequence, in situ hybridization: experimental and diagnostic applications.

Authors:  J M Davison; T W Morgan; B L Hsi; S Xiao; J A Fletcher
Journal:  Am J Pathol       Date:  1998-11       Impact factor: 4.307

5.  Recollections of a scientific journey published in human genetics: from chromosome territories to interphase cytogenetics and comparative genome hybridization.

Authors:  Thomas Cremer; Christoph Cremer; Peter Lichter
Journal:  Hum Genet       Date:  2014-02-07       Impact factor: 4.132

6.  Comparative genomic hybridization, loss of heterozygosity, and DNA sequence analysis of single cells.

Authors:  C A Klein; O Schmidt-Kittler; J A Schardt; K Pantel; M R Speicher; G Riethmüller
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-13       Impact factor: 11.205

7.  Correlation of microscopic phenotype with genotype in a formalin-fixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogenetics.

Authors:  M R Speicher; A Jauch; H Walt; S du Manoir; T Ried; W Jochum; T Sulser; T Cremer
Journal:  Am J Pathol       Date:  1995-06       Impact factor: 4.307

8.  Investigations with fluorescence in situ hybridization (FISH) demonstrate loss of the telomeres on the reciprocal chromosome in three unbalanced translocations involving chromosome 15 in the Prader-Willi and Angelman syndromes.

Authors:  A Jauch; L Robson; A Smith
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

9.  Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGH.

Authors:  H J Decker; C Neuhaus; A Jauch; M Speicher; T Ried; M Bujard; H Brauch; S Störkel; M Stöckle; B Seliger; C Huber
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

10.  Order of human hematopoietic growth factor and receptor genes on the long arm of chromosome 5, as determined by fluorescence in situ hybridization.

Authors:  P M Kluck; J Wiegant; A K Raap; H Vrolijk; H J Tanke; R Willemze; J E Landegent
Journal:  Ann Hematol       Date:  1993-01       Impact factor: 3.673

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