Summary
DNA rotational mobility in a bovine papilloma virus (BPV)-based minichromosome, autonomously replicating in mouse cells, was studied using topoisomer analysis in temperature shift experiments. It was found that in live cells the average number of topological turns increased by six in the course of temperature shift through a range of 37°C. This comprised approximately 85% of the total potential mobility of naked plasmid DNA. DNA rotation in isolated nuclei was found to be 3.5–4.0 turns per 37° C in 100 mM NaCl — much higher than in all experiments with animal cells reported thus far. In low salt mobility was considerably lowered. Attempts to extract minichromosomes from nuclei allowed isolation of no more than 10% of minichromosomal DNA, with could indicate a very high proportion of transcriptionally active minichromosomes in the intracellular population. Growing cells in the presence of sodium butyrate resulted not only in an increase in the level of plasmid superhelicity and a decrease of its transcription (as we report in the accompanying publication) but also reduced rotational mobility of plasmid DNA threefold (from 6 to 2 turns per 37° C). The decrease in DNA rotational mobility after butyrate treatment was also partially manifested in isolated nuclei (especially at lower ionic strength). To check whether histone acetylation is directly responsible for DNA immobilization, we performed in vitro acetylation of histories using acetyl adenylate. This resulted in severe DNA immobilization in experiments using both up and down temperature shifts.
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Communicated by G.P. Georgiev
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Krajewski, W.A., Luchnik, A.N. High rotational mobility of DNA in animal cells and its modulation by histone acetylation. Molec. Gen. Genet. 231, 17–21 (1991). https://doi.org/10.1007/BF00293816
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DOI: https://doi.org/10.1007/BF00293816