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Graduate School of Science, Department of Physics, Kyoto University, Sakyo-ku, Kyoto 608-8501, Japan; and "Spatio-Temporal Order" Project, International Collaboration Research Project, Japan Science and Technology Agency, Tokyo, Japan
Correspondence: Address reprint requests to Anatoly A. Zinchenko, E-mail: zinchenko{at}urban.env.nagoya-u.ac.jp.
We prepared complexes of giant double-stranded DNA with cationic nanoparticles of 1040 nm in diameter as an artificial model of chromatin and characterized the properties of changes in their higher-order conformation. We measured the changes in transcriptional activity that accompanied the DNA conformational transitions. Complete inhibition was found at excess concentrations of nanoparticles. In contrast, at intermediate stages of DNA binding with nanoparticles, the transcription activity of DNA survived, and this strongly depended on the size of the nanoparticles. For large nanoparticles of 40 nm, a decrease in transcriptional activity can be caused by the addition of only a small amount of nanoparticles. On the other hand, there was almost no inhibition of DNA transcriptional activity with the addition of small nanoparticles (10 nm) until very high concentrations, even under conditions that induced DNA compaction as revealed by single-DNA observation. At higher concentrations of 10-nm nanoparticles, DNA transcription activity decreased abruptly until it was completely inhibited. These results are discussed in relation to the actual size of the histone core, together with the mechanism of switching of transcriptional activity in eukaryotic cells.
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