Clipping of Flexible Tails of Histones H3 and H4 Affects the Structure and Dynamics of the Nucleosome  Nathan P. Nurse, Isabel Jimenez-Useche, Ian Tad.

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Clipping of Flexible Tails of Histones H3 and H4 Affects the Structure and Dynamics of the Nucleosome  Nathan P. Nurse, Isabel Jimenez-Useche, Ian Tad Smith, Chongli Yuan  Biophysical Journal  Volume 104, Issue 5, Pages 1081-1088 (March 2013) DOI: 10.1016/j.bpj.2013.01.019 Copyright © 2013 Biophysical Society Terms and Conditions

Figure 1 A schematic drawing of the closed and open conformations of a nucleosome that originates from the DNA end breathing motion observed at low salt concentrations. The H3 tails are shown as dashed lines and the H4 tails as solid lines (one H4 tail is only partially visible due to the orientation of the nucleosome). A symmetric breathing motion is pictured here, but a possible alternative model exists in which the DNA breathing occurs asymmetrically. In this case, only one of the DNA ends breathes away from the histone core at a time. The circles at the DNA ends depict the locations of the FRET dye pair. Biophysical Journal 2013 104, 1081-1088DOI: (10.1016/j.bpj.2013.01.019) Copyright © 2013 Biophysical Society Terms and Conditions

Figure 2 (a) The distance between the DNA ends for mononucleosomes in the closed conformation, d1, under different monovalent cationic conditions. (b) The distance between the DNA ends for mononucleosomes in the open conformation, d2. (c) The fraction of nucleosomes in the closed conformation, f1. (d) The apparent equilibrium constant, Kapparent, characterizing the DNA breathing motion under different KCl concentrations. The legend is the same for all four graphs. A t-test is applied to compare the statistical significance of the measurements in (a–c) for the four mononucleosomes. Each data point that is statistically different than WT is labeled based on the confidence level. The confidence levels are (∗) for 99% (p = .01) and (+) for 95% (p = .05). Unlabeled data points in (a–c) are not statistically different than WT at the 95% confidence level. f1 is the only parameter used to calculate Kapparent therefore the statistical significance is the same in (d) as it is in (c). Error bars are omitted from these graphs to avoid overcrowding. Graphs that include the error bars are available in Figs. S12, S14, and S16. Biophysical Journal 2013 104, 1081-1088DOI: (10.1016/j.bpj.2013.01.019) Copyright © 2013 Biophysical Society Terms and Conditions

Figure 3 (a) The distance between the DNA ends for mononucleosomes in the closed conformation, d1, under different divalent cationic conditions. (b) The distance between the DNA ends for mononucleosomes in the open conformation, d2. (c) The fraction of nucleosomes in the closed conformation, f1. (d) The apparent equilibrium constant, Kapparent, characterizing the DNA breathing motion under different MgCl2 concentrations. The legend is the same for all four graphs. A t-test is applied to compare the statistical significance of the measurements in (a–c) for the four mononucleosomes. Each data point that is statistically different than WT is labeled based on the confidence level. The confidence levels are (∗) for 99% (p = .01) and (+) for 95% (p = .05). Unlabeled data points in (a–c) are not statistically different than WT at the 95% confidence level. f1 is the only parameter used to calculate Kapparent therefore the statistical significance is the same in (d) as it is in (c). Error bars are omitted from these graphs to avoid overcrowding. Graphs that include the error bars are available in Figs. S13, S15, and S17. Biophysical Journal 2013 104, 1081-1088DOI: (10.1016/j.bpj.2013.01.019) Copyright © 2013 Biophysical Society Terms and Conditions