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In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus

Isolated macronuclei from the hypotrichous ciliated protozoan Euplotes eurystomus incorporate biotinylated dUTP specifically into the replication band (RB) as detected with immunofluorescence, using rabbit anti-biotin antibodies followed by fluorescein-conjugated goat anti- rabbit IgG. When gold-con...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1987
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114460/
https://www.ncbi.nlm.nih.gov/pubmed/3553204
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description Isolated macronuclei from the hypotrichous ciliated protozoan Euplotes eurystomus incorporate biotinylated dUTP specifically into the replication band (RB) as detected with immunofluorescence, using rabbit anti-biotin antibodies followed by fluorescein-conjugated goat anti- rabbit IgG. When gold-conjugated goat anti-rabbit IgG was used in a preembedded reaction, subsequent immunoelectron microscopic analysis demonstrated that the biotinylated nucleotide appeared more concentrated in the rear zone of the RB, with almost no labeling in the forward zone. It was possible to use the immunofluorescent assay to establish that incorporation of biotinylated dUTP is inhibited by simultaneous addition of N-ethyl maleimide or aphidicolin, and by omission of any one of the other unlabeled dNTPs. In addition, prolonged heat shock of the intact cells, before lysis and in vitro assay, yielded markedly reduced incorporation. Comparison with published data on the in vivo incorporation of [3H]thymidine into Euplotes eurystomus RBs indicates the fidelity of the in vitro reaction.
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spelling pubmed-21144602008-05-01 In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus J Cell Biol Articles Isolated macronuclei from the hypotrichous ciliated protozoan Euplotes eurystomus incorporate biotinylated dUTP specifically into the replication band (RB) as detected with immunofluorescence, using rabbit anti-biotin antibodies followed by fluorescein-conjugated goat anti- rabbit IgG. When gold-conjugated goat anti-rabbit IgG was used in a preembedded reaction, subsequent immunoelectron microscopic analysis demonstrated that the biotinylated nucleotide appeared more concentrated in the rear zone of the RB, with almost no labeling in the forward zone. It was possible to use the immunofluorescent assay to establish that incorporation of biotinylated dUTP is inhibited by simultaneous addition of N-ethyl maleimide or aphidicolin, and by omission of any one of the other unlabeled dNTPs. In addition, prolonged heat shock of the intact cells, before lysis and in vitro assay, yielded markedly reduced incorporation. Comparison with published data on the in vivo incorporation of [3H]thymidine into Euplotes eurystomus RBs indicates the fidelity of the in vitro reaction. The Rockefeller University Press 1987-05-01 /pmc/articles/PMC2114460/ /pubmed/3553204 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus
title In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus
title_full In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus
title_fullStr In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus
title_full_unstemmed In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus
title_short In vitro DNA synthesis in the macronuclear replication band of Euplotes eurystomus
title_sort in vitro dna synthesis in the macronuclear replication band of euplotes eurystomus
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114460/
https://www.ncbi.nlm.nih.gov/pubmed/3553204