
Base J or beta-d-glucosylhydroxymethyluracil is a DNA modification replacing a fraction of thymine in the nuclear DNA of kinetoplastid parasites and of Euglena. J is located in the telomeric sequences of Trypanosoma brucei and in other simple repeat DNA sequences. In addition, J was found in the inactive variant surface glycoprotein (VSG) expression sites, but not in the active expression site of T. brucei, suggesting that J could play a role in transcription silencing in T. brucei. We have now looked at the distribution of J in the genomes of other kinetoplastid parasites. First, we analyzed the DNA sequences immunoprecipitated with a J-antiserum in Leishmania major Friedlin. Second, we investigated the co-migration of J- and telomeric repeat-containing DNA sequences of various kinetoplastids using J-immunoblots and Southern blots of fragmented DNA. We find only approximately 1% of J outside the telomeric repeat sequences of Leishmania sp. and Crithidia fasciculata, in contrast to the substantial fraction of non-telomeric J found in T. brucei, Trypanosoma equiperdum and Trypanoplasma borreli. Our results suggest that J is a telomeric base modification, recruited for other (unknown) functions in some kinetoplastids and Euglena.
Leishmania, Trypanosoma cruzi, Immunoblotting, Crithidia fasciculata, Sequence Analysis, DNA, DNA, Protozoan, Telomere, Chromatography, Agarose, Glucosides, Animals, Immunoprecipitation, Uracil, Molecular Biology, Genome, Protozoan, Repetitive Sequences, Nucleic Acid
Leishmania, Trypanosoma cruzi, Immunoblotting, Crithidia fasciculata, Sequence Analysis, DNA, DNA, Protozoan, Telomere, Chromatography, Agarose, Glucosides, Animals, Immunoprecipitation, Uracil, Molecular Biology, Genome, Protozoan, Repetitive Sequences, Nucleic Acid
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