In-situ hybridization probes for identification and banding of s

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing compound containing saccharide radical

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435 6, 536 243, 536 2431, C12P 1934, C12Q 168, C07H 2104

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055388698

ABSTRACT:
The invention relates to novel primer sets useful in preparing DNA probes specific for any chromosome or part of a chromosome, particularly human chromosomes. The DNA probes so produced may be used to paint individual chromosomes or portions of chromosomes in metephase cell spreads and in interphase nuclei. When used to paint chromosomes in metephase spreads, R-bands are readily detectable. The method is sensitive and has been shown to paint R-bands on chromosomes pieces having as few as several hundred kilobases.

REFERENCES:
patent: 4683195 (1987-07-01), Mullis et al.
Jones and Winistorfer, 1992. "Sequence specific generation of a DNA panhandle permits PCR amplification of unknown flanking DNA," Nucleic Acids Research, 20(3):595-600.
Ledbetter et al., (1990). "Rapid Isolation of DNA Probes within Specific Chromosome Regions by Interspersed Repetitive Sequence Polymerase Chain Reaction," Genomics, V. 6:475-481.
Ochman et al., 1988. "Genetic Applications of an Inverse Polymerase Chain Reaction," Genetics, 120:621-623.
Sugimoto and Himeno, 1991. "A Rapid Isolation of the Unknown 5'-Flanking Sequence of Human CENP-B cDNA with Polymerase Chain Reactions," Agric. Biol. Chem., 55(11):2687-2692.
Trigira et al., 1988. "A procedure for in vitro amplification of DNA segments that lie outside the boundaries of known sequences," Nucleic Acids Research, 16(16):8186.
Dionne et al., 1990. "Chromosome Assignment by Polymerase Chain Reaction Techniques: Assignment of the Oncogene FGF-5 to Human Chromosome 4," BioTechniques, 8(2):190-194.
Iggo et al., 1989. "Chromosome mapping of the human gene encoding the 68-kDa nuclear antigen (p68) by using the polymerase chain reaction," Proc. Natl. Acad. Sci. USA, 86:6211-6214.
Nelson et al., 1989. "Alu polymerase chain reaction: A method for rapid isolation of human-specific sequences from complex DNA sources," Proc. Natl. Acad. Sci. USA, 86:6686-6690.
Lichter et al., 1988. "Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries," Hum. Genet., 80:224-234.
Hochgeschwender et al., 1989. "Construction and screening of a genomic library specific for mouse chromosome 16," Proc. Natl. Acad. Sci. USA, 86:8482-8486.
Kariya et al., 1987. "Revision of consensus sequence of human Alu repeats--a review," Gene, 53:1-10.
Tkachuk et al., 1990. "Detection of bcr-abl Fusion in Chronic Myelogeneous Leukemia by in Situ Hybridization," Science, 250:559-566.
Trent et al., 1989. "Report of the committee on structural chromosome changes in neoplasia," Cytogenet. Cell Genet., 51:533-562.
Harper et al., 1989. "Report of the committee on clinical disorders and chromosomal deletion syndromes," Cytogenet. Cell Genet., 51:563-611.
Rowley, Janet D., 1973. "A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining," Nature, 243:290-293.
de Klein et al., 1982. "A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelogenous leukemia," Nature, 300:765-767.
Heisterkamp et al., 1983. "Localization of the c-abl oncogene adjacent to a translocation break point in chronic myelocytic leukaemia," Nature, 306:239-242.
Seabright, M., 1971. "A rapid banding technique for human chromosome," Lancet., 2:971-972.
Sumner et al., 1971. "New technique for distinguishing between human chromosomes," Nat. New Biol., 232:31-72.
Pinkel et al., 1988. "Fluorescence in-situ hybridization with human chromosome-specific libraries: detection of trisomy and translocations of chromosome 4," Proc. Natl. Acad. Sci. USA, 85:9138-9142.
Lichter et al., 1988. "Rapid detection of human chromosome 21 aberrations by in-situ hybridization," Proc. Natl. Acad. Sci. USA, 85:9664-9668.
Pinkel et al., 1986. "Cytogenetic analysis using quantitative, high sensitivity, fluorescence hybridization," Proc. Natl. Acad. Sci. USA, 83:2934-2938.
Zhao et al., 1990. "Detection of t(9;22) in chromonic myelogenous leukemia by fluorescence in-situ hybridization with chromosome-specific composite probes," Am. J. Hum. Genet., 47:A119.
Kuo et al., 1990. "Clinical cytogenetic diagnosis with chromosome-specific DNA probes," Am. J. Hum. Genet., 47:A119.
Le Beau et al., 1983. "Associations of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia," N. Engl. J. Med., 309:630-636.
Jelinek et al., 1980. "Ubiquitous interspersed repeated sequences in mammalian genomes," Proc. Natl. Acad. Sci. USA, 77:1398-1402.
Breukel et al., 1990. "Vector-Alu PCR: a rapid step in mapping cosmids and YACs," NAR, 18:3097.
Brooks-Wilson et al., 1990. "Rapid cloning and characterization of new chromosome 10 DNA markers by Alu element-mediated PCR," Genomics.
Cotter et al., 1990. "Rapid isolation of human chromosome-specific DNA probes from a somatic cell hybrid," Genomics, 7:257-263.
Glover et al., 1990. "Construction of irradiation-reduced hybrids for human chromosome 3 and characterization by IRS-PCR (interspersed repetitive sequence PCR) analysis," Am. J. Hum. Genet., 47:A91.
Kievits et al., 1990. "Direct nonradioactive in-situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes," Cytometry, 11:105-109.
Dauwerse et al., 1990. "Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p," Cytogenet. Cell Genet., 53:126-128.
Meyne and Moyzis, 1989. "Human chromosome-specific repetitive DNA probes: Targeting in-situ hybridization to chromosome 17 with a 42-base-pair alphoid DNA oligomer." Genomics, 4:472-478.
Deininger and Schmid, 1979. "A study of the evolution of repeated DNA sequences in primates and the existence of a new class of repetitive sequences in primates," J. Mol. Biol., 127:437-460.
Singer, 1982. "Highly repeated sequences in mammalian genomes (review)," Intl. Rev. Cytol., 76:67-112.
Manuelidis and Ward, 1984. "Chromosomal and nuclear distribution of the Hind III 1.9-kb human DNA repeat segment," Chromosoma, 91:28-38.
Burke et al., 1987. "Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors," Science, 236:806-812.
Ludecke et al., 1989. "Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification," Nature, 338:348-340.
Denninger et al., 1981. "Base sequence studies of 300 nucleotide renatured repeated human DNA clones," J. Mol. Bio., 151:17-33.
Goldberg et al., 1979. "Isolation of specific RNAs using DNA covalently linked to diazobenzyloxymethyl cellulose or paper," Methods in Enzymology, 68:206-220.
Noyes and Stark, 1975. "Nucleic acid hybridization using DNA covalently coupled to cellulose," Cell, 5:301-310.
Brison et al., 1982. "General method for cloning amplified DNA by differential screening with genomic probes," Mol. Cell Biol., 2:578-587.
Blin and Stafford, 1976. "A general method for isolation of high molecular weight DNA from eukaryotes," Nuc. Acid Res., 3:2303-2308.
van Ommen and Verkerk, 1986. "Human Genetic Diseases, A Practical Approach," ed. by K. E. Davies, 1986, IRL Press, Oxford, England.
Johnson, and de Aroujo, 1981. "A simple method of reducing the faking of immunofluorescence during microscopy," J. Immunol. Methods, 43:349-350.
Thompson et al., 1989. "Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19," Genomics, 5:670-679.
Liu et al., 1989. "Human DNA excision repair gene ERCC4 is located on chromosome 16 short arm 16p13.13-p13.3," Cytogenet, Cell Genet., 51:1035.
Liu et al., 1989. "Isolation of human transcribed sequences from human-rodent somatic cell hybrids," Science, 246:813-815.
Stallings et al., 1988. "Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for muscle form to the genes for apolipoprotein C2 and excision repair," Am. J. Hum. Genet., 43:144-151.
Thompson et al., 1985. "Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells," Somat. Cell Molec. Genet., 11:87

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