In situ hybridization of DNA sequences in human metaphase chromosomes visualized by an indirect fluorescent immunocytochemical procedure

• Published in: Experimental cell research Vol. 141; no. 2; pp. 397 - 407
• Main Authors: Van Prooijen-Knegt, A.C., Van Hoek, J.F.M., Bauman, J.G.J., Van Duijn, P., Wool, I.G., Van der Ploeg, M.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.10.1982
• Subjects: Base Sequence; Chromosome Mapping; Chromosomes, Human; DNA; Endopeptidase K; Endopeptidases; Fluorescent Antibody Technique; Genes; Humans; Metaphase; Microscopy, Fluorescence; Nucleic Acid Hybridization; RNA, Ribosomal - genetics; Temperature
• ISSN: 0014-4827; 1090-2422
• DOI: 10.1016/0014-4827(82)90228-2

In situ hybridization and immunocytochemical procedures are described which allow identification and localization of specific DNA sequences in human chromosomes by fluorescence microscopy. With this method the genes coding for 18S and 28S ribosomal RNA (rRNA) were localized on human metaphase chromosomes by in situ hybridization of 18S or 28S rRNA followed by an immunocytochemical incubation with specific anti-RNA-DNA hybrid antiserum. Visualization of the immunocytochemically localized RNA-DNA hybrids was achieved by indirect immuno-fluorescence. The antiserum against RNA-DNA hybrid molecules was raised in a rabbit injected with poly(rA)-poly(dT). The specificity of the sera was determined using a model system of Sephadex beads to which various nucleic acids had been coupled. To obtain optimal specific fluorescence and very low aspecific background staining, several modifications of the in situ hybridization and the immunocytochemical procedures were investigated. The use of aminoalkylsilane-treated glass slides, removal of unbound fluorochrome molecules from the fluorochromelabelled antibody solutions and application of a proteinase K treatment during the hybridization procedure and the immunocytochemical procedure proved to be essential for optimal results.