CO-FISH reveals inversions associated with isochromosome formation

Mutagenesis

Volumn 11, Issue 2, 1996, Pages 139-144

  Bailey, S M ^a   Goodwin, E H ^a   Meyne, J ^a   Cornforth, M N ^b  

^a LOS ALAMOS NATIONAL LABORATORY   (United States)

^b University of Texas Medical Branch School of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA; SINGLE STRANDED DNA;

ARTICLE; CELL LINE; CHROMOSOME INVERSION; CONTROLLED STUDY; DNA PROBE; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; ISOCHROMOSOME; PRIORITY JOURNAL; TELOMERE;

BASE SEQUENCE; CELL LINE; CHROMOSOMES, HUMAN, PAIR 18; DNA PROBES; DNA, SINGLE-STRANDED; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; ISOCHROMOSOMES; METAPHASE; MOLECULAR SEQUENCE DATA;

EID: 0029939172     PISSN: 02678357     EISSN: None     Source Type: Journal    
DOI: 10.1093/mutage/11.2.139     Document Type: Article

References (28)

1. Blackburn,E.H. and Szostak,J W. (1984) The molecular structure of centromeres and telomeres. Annu. Rev. Biochem., 53, 163-194.
2. Fan,Y., Davis,L.M. and Shows,T.B. (1990) Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. Proc. Nail Acad. Sci. USA, 87, 6223-6227.
3. Goodwin,E, and Meyne,J. (1993) Strand-specific FISH reveals orientation of chromosome 18 alphoid DNA. Cytogenet. Cell Genet., 63, 126-127.
4. Goto,K., Maeda,S., Kano,Y. and Sugiyama,T. (1978) Factors involved in differential Giemsa-staining of sister chromatids. Chromosoma. 66, 351-359 .
5. Hayata,I. (1993) Removal of stainable cytoplasmic substances from cytogenetic slide preparations. Biotech. Histochem., 68, 150-152.
6. Heppel-Parton,A.C., Albenson,D.G., Fishpool,R. and Rabbitts,P.H. (1994) Multicolor fluorescence in situ hybridization to order small, single-copy probes on metaphase chromosomes. Cytogen. Cell Genet., 66, 42-47.
7. Johnson,G.D. and Nogueira Araujo,G.M. (1981) A simple method of reducing fading of immunofluorescence during microscopy. J. Immunol. Methods, 43, 349-350.
8. Latt,S.A. (1973) Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes. Proc. Natl Acad. Sci. USA, 70, 3395-3399.
9. LeBeau,M.M., Larson,R.A., Bitter,M.A., Vardiman.J.W., Golomb,H M. and Rowley,J.D. (1983) Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. N. Engl. J. Med., 309, 630-636.
10. Lucas,J.N. and Sachs,R.K. (1993) Using three-color chromosome painting to test chromosome aberration models. Proc. Natl Acad. Sci. USA, 90, 1484-1487.
11. Meyne,J. and Goodwin,E.H. (1995) Direction of DNA sequences within chromatids determined using strand-specific FISH. Chromosome Res., 3, 375-378.
12. Meyne,J. and Moyzis,R.K. (1994) In situ hybridization using synthetic oligomeres as probes for centromere and telomere repeats. In Choo.K.H.A. (ed), Methods in Molecular Biology. Humana Press, Totowa, NJ, vol. 33, pp. 63-74.
13. Meyne,J., Littlefield,L.G. and Moyzis,R.K. (1989a) Labeling of human centromeres using alphoid DNA consensus sequence: application to the scoring of chromosome aberrations. Mutat. Res., 226, 75-79.
14. Meyne,J., Ratliff,R.L. and Moyzis,R.K. (1989b) Conservation of the human telomere sequence (TTAGGG)n among vertebrates Proc. Natl Acad. Sci. USA. 86, 7049-7053.
15. Mishra,N.C. (1995) Molecular Biology of Nucleuses. CRC Press, New York, pp. 47-49.
16. Moyzis,R.K., Buckingham,J.M., Cram,L.S., Dani,M., Deaven,L.L., Jones,M.D., Meyne,J., Ratliff,R L and Wu,J.R. (1988) A highly conserved repetitive DNA sequence. (TTAGGG)n, present at the telomeres of human chromosomes. Proc. Natl Acad. Sci. USA. 85, 6622-6626
17. Mühlmann-Diaz,M.C. and Bedford,J.S. (1995) Comparison of gamma-ray-induced chromosome ring and inversion frequencies. Radiol. Res., 143, 175-180.
18. NIGMS (1992/1993) National Institutes of Health. National Institute of General Medical Sciences, Human Genetic Mutant Cell Respository Publication number 92-2011.
19. Pinkel,D., Straume,T. and Gray,J.W. (1986) Cytogenetic analysis using quantitative, high-sensitivity. fluorescence hybridization. Proc. Natl Acad. Sci USA, 83, 2934-2938.
20. Pinkel,D., Landegent,J., Collins,C., Fuscoe,J., Seagraves,R., Lucas,J. and Gray,J. (1988) Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. Proc. Natl Acad. Sci. USA, 85, 9138-9142.
21. Saito,H., Hayday,A., Wiman,K., Hayward, W and Tonegawa,S. (1983) Activation of the c-myc gene by translocation: a model for translational control. Proc. Nail Acad. Sci. USA, 80, 7476-7480.
22. Savage,J.R.K. (1977) Assignment of aberration break points in banded chromosomes. Nature. 270 513-514.
23. Stebbins,G.L. (1950) Variation and Evolution in Plants. Columbia University Press. New York
24. ThackerJ (1986) The nature of mutants induced by ionising radiation in cultured hamster cells III. Molecular characterization of HPRT-deficient mutants induced by γ-rays and α-particles showing that the majority have deletions of all or part of the hprt gene. Mutat. Res., 160, 267-275.
25. Urlaub,G., Mitchell,P.J., Kas,E., Chasin,L.A., Funanage,V.L., Myoda,T.T. and HamlinJ. (1986) Effect of gamma rays at the dihydrofolate reductase locus: deletions and inversions. Somat. Cell Mol. Genet., 12, 555-566.
26. van Dekken, H., Pinkel, D., Mullikin, J. and Gray, J.W. (1988) Enzymatic production of single-stranded DNA as a target for fluoresence in situ hybridization. Chromosoma (Berl.) 97, 1-5.
27. Zakhorov,A.F. and Egolina,N.A. (1972) Differential spiralization along mammalian mitotic chromosomes, i. BUdr-revealed differentiation in Chinese hamster chromosomes. Chromosoma. 38, 341-365.
28. Zech,L., Godal,T., Hammarström,L., Mellstedt,H., Smith,C.I.E., Tötterman,T. and Went,M. (1986) Specific chromosome markers involved with chronic T-lymphocyte tumors. Cancer Genet. Cytogenet., 21, 67-77.