Detection of karyotype changes in interphase cells: Oligonucleotide-primed in situ labelling versus fluorescence in situ hybridization

Virchows Archiv

Volumn 430, Issue 5, 1997, Pages 381-387

  Werner, Martin ^a   Wilkens, Ludwig ^b   Nasarek, Anette ^b   Tchinda, Joëlle ^b   Komminoth, Paul ^c  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^b HANNOVER MEDICAL SCHOOL   (Germany)

^c UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

Chromosomes; Hepatocellular carcinoma; In situ hybridization; Leukaemia; Molecular cytogenetics

Indexed keywords

DNA POLYMERASE; OLIGONUCLEOTIDE;

ARTICLE; BONE MARROW; CENTROMERE; CONTROLLED STUDY; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERPHASE; KARYOTYPE; LYMPHOCYTE CULTURE; METAPHASE; PRIORITY JOURNAL;

BIOPSY; BONE MARROW; CELL NUCLEUS; CHROMOSOMES; DNA PRIMERS; HUMANS; IN SITU HYBRIDIZATION; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; KARYOTYPING; LEUKEMIA, NONLYMPHOCYTIC, ACUTE; LIVER; LYMPHOCYTES; TRISOMY;

EID: 0030920104     PISSN: 09456317     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004280050047     Document Type: Article

References (28)

1. Bernhards J, Weitzel B, Werner M, Rimpler M, Georgii A (1992) A new histological embedding method by low-temperature polymerisation of methyl methacrylate allowing immuno- and enzyme histochemical studies on semi-thin sections of undecalcified bone marrow biopsies. Histochemistry 98:145-154
2. Brandt CA, Kierkegaard O, Hindkjaer J, Jensen PKA, Pedersen S, Therkelsen AJ (1993) Ring chromosome 20 with loss of telomeric sequences detected by multicolour PRINS. Clin Genet 44:26-31
3. Brandt CA, Djernes B, Stromkjaer H, Petersen MB, Pedersen S, Hindkjaer J, Brinch-Iversen J, Bruun-Petersen G (1994) Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS). J Med Genet 31:99-102
4. Cinti C, Santi S, Maraldi NM (1993) Localization of single copy gene by PRINS technique. Nucleic Acids Res 21:5799-5800
5. Gosden J, Lawson D (1995) Rapid chromosome identification by oligonucleotide-primed in situ DNA synthesis (PRINS). Hum Mol Genet 3:931-936
6. Gosden J, Lawson D (1995) Instant PRINS: a rapid method for chromosome identification by detecting repeated sequences in situ. Cytogenet Cell Genet 68:57-60
7. Hindkjaer J, Koch J, Mogensen J, Kolvraa S, Bolund L (1994) Primed in situ (PRINS) labelling of DNA. Methods Mol Biol 33:95-106
8. Hindkjaer J, Hammoudah SA, Hansen KB, Jensen PD, Koch J, Pedersen B (1995) Translocation (1;16) identified by chromosome painting and PRimed IN Situ-labelling (PRINS). Report of two cases and review of the cytogenetic literature. Cancer Genet Cytogenet 79:15-20
9. Joos S, Fink TM, Ratsch A, Lichter P (1994) Mapping and chromosome analysis: the potential of fluorescence in situ hybridization. J Biotech 35:135-153
10. Klinger K, Landes G, Shook D, Harvey R, Lopez L, Locke P, Lerner T, Osathanondh R, Leverone B, Houseal T, Pavelka K, Dackowski W (1992) Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization. Am J Hum Genet 51:55-65
11. Koch JE, Kolvraa S, Petersen KB, Gregersen N, Bolund L (1989) Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ. Chromosoma 98:259-265
12. Koch JE, Hindkjaer J, Mogensen J, Kolvraa S, Bolund L (1991) An improved method for chromosome specific labelling of alpha satellite DNA in situ by using denatured double-stranded DNA probes as primers in a primed in situ labelling (PRINS) procedure. Genet Anal Tech Appl 8:171-178
13. Koch J, Mogensen J, Pedersen S, Fischer H, Hindkjaer J, Kolvraa S, Bolund L (1992) Fast one step procedure for the detection of nucleic acids in situ by primer-induced sequence-specific labelling with fluorescein-12-dUTP. Am J Hum Genet 51:55-65
14. Koch J, Fischer H, Askholm H, Hindkjaer J, Pedersen S, Kolvraa S, Bolund L (1993) Identification of a supernumerary der(18) chromosome by a rational strategy for the cytogenetic typing of small marker chromosomes with chromosome-specific DNA probes. Clin Genet 43:200-203
15. Moyzis RK, Buckingham JM, Cram LS, Dani M, Deaven LL, Jones MD, Meyne J, Rattliff RL, Wu J-R (1988) A highly conserved repetitive DNA sequence (TTAGGG)n, present at the telomeres of human chromosomes. Proc Natl Acad Sci, USA: 662-666
16. Nasarek A, Werner M, Nolte M, Klempnauer J, Georgii A (1995) Trisomy 1 and 8 occur frequently in hepatocellular carcinoma but not in liver cell adenoma and focal nodular hyperplasia. A fluorescence in situ hybridization study. Virchows Arch 427:373-378
17. Pellestor F, Girardet A, Lefort G, Andreo B, Charlieu JP (1994) Rapid in situ detection of chromosome 21 by the PRINS technique. Ann Genet 37:66-71
18. Pellestor F, Girardet A, Lefort G, Andreo B, Charlieu JP (1995) Rapid in situ detection of chromosome 21 by the PRINS technique. Am J Med Genet 56:393-397
19. Pellestor F, Quennesson I, Coignet L, Girardet A, Andreo B, Lefort G Charlieu JP (1996) FISH and PRINS, a strategy for rapid chromosome screening: application to the assessment of aneuploidy in human sperm. Cytogenet Cell Genet 72:34-36
20. Pinkel D, Straume T, Gray JW (1986) Cytogenetic analysis using quantitative, high-sensitivity fluorescence hybridization. Proc Natl Acad Sci USA 83:2934-2938
21. Raap AK, Corput MPC van de, Vervenne RAW, Gijlwikj RPM van, Tunke HJ, Wiegand J (1995) Ultra-sensitive FISH using peroxidase-mediated deposition of biotin or fluorochrome tyramides. Hum Mol Genet 4:529-534
22. Rowley JD (1990) Recurring chromosome abnormalities in leukaemia and lymphoma. Semin Hematol 27:122-136
23. Terkelsen C, Koch J, Kolvraa S, Hindkjaer J, Pedersen S, Bolund L (1993) Repeated primed in situ labelling: formation and labelling of specific DNA sequences in chromosomes and nuclei. Cytogenet Cell Genet 63:235-237
24. Tkachuk DC, Westbrook CA, Andreef M, Conlon TA, Cleary ML, Suryanarayan K, Homge M, Redner A, Gray J, Pinkel D (1990) Detection of bcr-abl fusion in chronic myelogenous leukaemia by in situ hybridization. Science 250:559-562
25. Ward BE, Gersen SL, Carelli MP, McGuire NM, Dackowski WR, Weinstein M, Sandlin C, Warren R, Klinger KW (1993) Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens. Am J Hum Genet 52:854-865
26. Waye JS, Willard HF (1987) Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes. Nucleic Acids Res 15:7549-7567
27. Werner M, Kaloutsi V, Buhr T, Delventhal S, Vykoupil KF, Georgii A (1991) Cytogenetics of chronic myelogenous leukaemia correlated to the histopathology of bone marrow biopsies. Ann Hematol 63:201-205
28. Werner M, Wasielewski R v, Komminoth P (1996) Antigen retrieval, signal amplification and intensification in immunohistochemistry. Histochem Cell Biol 105:253-260