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

SummaryWe 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.

[1]  M. Leppert,et al.  R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1) , 1990, Human Genetics.

[2]  J. Mallet,et al.  Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization. , 1991, Genomics.

[3]  H. Willard,et al.  Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. , 1988, Cancer research.

[4]  J. Yu,et al.  Chromosome microdissection and cloning in human genome and genetic disease analysis. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[5]  H. Riethman,et al.  Painting of human chromosomes with probes generated from hybrid cell lines by PCR with Alu and L1 primers , 2004, Human Genetics.

[6]  H. Tanke,et al.  Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridization. , 1989, Cancer genetics and cytogenetics.

[7]  P. Nederlof,et al.  Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences. , 1989, Cytometry.

[8]  J. Garson,et al.  Novel non-isotopic in situ hybridization technique detects small (1 Kb) unique sequences in routinely G-banded human chromosomes: fine mapping of N-myc and beta-NGF genes. , 1987, Nucleic acids research.

[9]  P. Lichter,et al.  Painting of defined chromosomal regions by in situ suppression hybridization of libraries from laser-microdissected chromosomes. , 1991, Cytogenetics and cell genetics.

[10]  D. Ward,et al.  Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries , 1988, Human Genetics.

[11]  M. Oshimura,et al.  Construction of Mouse A9 Clones Containing a Single Human Chromosome Tagged with Neomycin‐resistance Gene via Microcell Fusion , 1989, Japanese journal of cancer research : Gann.

[12]  D. Pinkel,et al.  Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[13]  L. Manuelidis,et al.  Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes , 1988, Human Genetics.

[14]  P. Lichter,et al.  Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization. , 1990, Cytometry.

[15]  A. Jauch,et al.  Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics , 1990, Human Genetics.

[16]  B. Horsthemke,et al.  Construction and characterization of band-specific DNA libraries , 1990, Human Genetics.

[17]  Bernhard Horsthemke,et al.  Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification , 1989, Nature.