• 1 January 1980
    • journal article
    • research article
    • Vol. 20  (3) , 290-296
Abstract
Pairs of fluorescent A-T [adenine, thymine] specific dyes and nonfluorescent agents with similar or complementary base pair binding specificity were used to analyze the extent to which banding patterns in human chromosomes obtained by fluorescent staining can be modified by counterstaining. By testing a variety of different combinations of drugs, essentially 3 types of alterations were observed. Enhanced contrast of specific heterochromatic regions was obtained with pentamidine or netropsin in conjunction with the fluorescent stains Hoechst 33258, DAPI [4'',6-diamidino-2-phenylindole] or DIPI [4'',6-bis-diimidazolo-2-phenylindole] the resulting banding patterns being similar to that reported for distamycin A plus DAPI (DA-DAPI banding). Uniform quenching of Hoechst 33258, DAPI or DIPI fluorescence was induced by counterstaining with stilbamidine or berenil. The combination of echinomycin with DAPI resulted in an improved contrast of DAPI banding on chromosome arms and pale fluorescence on major autosomal C band regions. A subdivision of the heterochromatic part of the Y chromosome may be discerned by this latter technique. [Mouse chromosomes were also studied.].