Monitoring genomic alterations with a panel of oligonucleotide probes specific for various simple repeat motifs

Germline and somatic instability of the human genome was studied, using synthetic oligonucletides specific for simple repeat motifs. The following probes were used: (GTG)5, (GACA)4, (GATA)4, (CT)8, (TTAGGG)3, (GT)8, (GAA)6 and (GGAT)4. Each of them is unique with respect to the target regions recognized in the genome. Thus compilation of the various fingerprint data provides a complex map of the genome (and its deviations). While the fingerprints of differentiated somatic tissues never showed any alterations, in tumor tissues (namely gliomas) many changes could be detected. Most of the latter reflect secondary karyological aberrations. In nearly one third of the gliomas, drastically amplified and apparently monomorphic DNA fragments were identified. This marker should make it possible to deal with causal pathogenetic mechanisms as well as novel diagnostic strategies.

[1]  M. Schmid,et al.  Chromosomal organization of simple repeated DNA sequences , 1991, Electrophoresis.

[2]  L. Roewer,et al.  Stain analysis using oligonucleotide probes specific for simple repetitive DNA sequences. , 1990, Forensic science international.

[3]  B. Vogelstein,et al.  A genetic model for colorectal tumorigenesis , 1990, Cell.

[4]  C. Harley,et al.  Telomeres shorten during ageing of human fibroblasts , 1990, Nature.

[5]  A. Poustka,et al.  Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping , 1990, Nature.

[6]  R. Myers,et al.  Structure and variability of human chromosome ends , 1990, Molecular and cellular biology.

[7]  R. Sager Tumor suppressor genes: the puzzle and the promise. , 1989, Science.

[8]  M. Oishi,et al.  A tissue-specific change in repetitive DNA in rats. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[9]  P. Green,et al.  Simultaneous genetic mapping of multiple human minisatellite sequences using DNA fingerprinting. , 1989, Genomics.

[10]  R. Moyzis,et al.  Conservation of the human telomere sequence (TTAGGG)n among vertebrates. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[11]  J. Goodfellow,et al.  Solvent interactions stabilising nucleic acid conformers. , 1989, Nucleic acids research.

[12]  F. Alt,et al.  Mechanism and developmental program of immunoglobulin gene rearrangement in mammals. , 1989, Annual review of genetics.

[13]  R. Allshire,et al.  Human telomeres: fusion and interstitial sites. , 1989, Trends in genetics : TIG.

[14]  V A Zakian,et al.  Structure and function of telomeres. , 1989, Annual review of genetics.

[15]  D. de Jong,et al.  Somatic changes in B-lymphoproliferative disorders (B-LPD) detected by DNA-fingerprinting. , 1988, British Journal of Cancer.

[16]  A. Jeffreys,et al.  Clustering of hypervariable minisatellites in the proterminal regions of human autosomes. , 1988, Genomics.

[17]  M. Fey,et al.  Assessment of clonality in gastrointestinal cancer by DNA fingerprinting. , 1988, The Journal of clinical investigation.

[18]  J. Epplen On simple repeated GATCA sequences in animal genomes: a critical reappraisal. , 1988, The Journal of heredity.

[19]  C. James,et al.  Clonal genomic alterations in glioma malignancy stages. , 1988, Cancer research.

[20]  D. de Jong,et al.  Analysis of tumor heterogeneity in a patient with synchronously occurring female genital tract malignancies by DNA flow cytometry, dna fingerprinting, and immunohistochemistry , 1988, Cancer.

[21]  H. Zischler,et al.  Optimized oligonucleotide probes for DNA fingerprinting , 1988, Electrophoresis.

[22]  L. Peltonen,et al.  Differences in DNA-fingerprints between remission and relapse in childhood acute lymphoblastic leukemia. , 1988, Leukemia research.

[23]  K. Kinzler,et al.  Relationship between gene amplification and chromosomal deviations in malignant human gliomas. , 1987, Cancer genetics and cytogenetics.

[24]  M. Georges,et al.  DNA fingerprinting in man using a mouse probe related to part of the Drosophila 'Per' gene. , 1987, Nucleic acids research.

[25]  A. Jeffreys,et al.  Detection of somatic changes in human cancer DNA by DNA fingerprint analysis. , 1987, British Journal of Cancer.

[26]  M. Georges,et al.  A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA. , 1987, Science.

[27]  P. Meltzer,et al.  Amplification units containing human N-myc and c-myc genes. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[28]  A. Knudson Hereditary cancer, oncogenes, and antioncogenes. , 1985, Cancer research.

[29]  Swee Lay Thein,et al.  Hypervariable ‘minisatellite’ regions in human DNA , 1985, Nature.

[30]  A. Tulusan,et al.  Incidence of double minutes, cytogenetic equivalents of gene amplification, in human carcinoma cells , 1984, International journal of cancer.

[31]  J. Yunis The chromosomal basis of human neoplasia. , 1983, Science.

[32]  A. Spradling,et al.  Amplification of genes for chorion proteins during oogenesis in Drosophila melanogaster. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[33]  F Vogel,et al.  Spontaneous mutation in man. , 1975, Advances in human genetics.

[34]  I. Dawid,et al.  Specific gene amplification in oocytes. Oocyte nuclei contain extrachromosomal replicas of the genes for ribosomal RNA. , 1968, Science.