Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA.
Phys Biol. 2012 Dec;9(6):065001. doi: 10.1088/1478-3975/9/6/065001. Epub 2012 Nov 29.
AFM images show that chromatin reconstituted on methylated DNA (meDNA) is compacted when imaged under water. Chromatin reconstituted on unmethylated DNA is less compacted and less sensitive to hydration. These differences must reflect changes in the physical properties of DNA on methylation, but prior studies have not revealed large differences between methylated and unmethylated DNA. Quasi-elastic light scattering studies of solutions of methylated and unmethylated DNA support this view. In contrast, AFM images of molecules at a water/solid interface yield a persistence length that nearly doubles (to 92.5 ± 4 nm) when 9% of the total DNA is methylated. This increase in persistence length is accompanied by a decrease in contour length, suggesting that a significant fraction of the meDNA changes into the stiffer A form as the more hydrophobic meDNA is dehydrated at the interface. This suggests a simple mechanism for gene silencing as the stiffer meDNA is more difficult to remove from nucleosomes.
原子力显微镜图像显示,在水中成像时,组蛋白在甲基化 DNA(meDNA)上重建的结构是紧凑的。而在非甲基化 DNA 上重建的组蛋白则不太紧凑,对水合作用也不那么敏感。这些差异必然反映了 DNA 在甲基化过程中物理性质的变化,但先前的研究并未揭示甲基化和非甲基化 DNA 之间存在显著差异。甲基化和非甲基化 DNA 溶液的准弹性光散射研究支持了这一观点。相比之下,当总 DNA 的 9%被甲基化时,在水/固界面处的分子的原子力显微镜图像的持久长度几乎增加了一倍(至 92.5±4nm)。这种持久长度的增加伴随着轮廓长度的减小,表明作为更疏水的 meDNA 在界面处脱水,相当一部分的 meDNA 转变为更坚硬的 A 形式。这表明了一种简单的基因沉默机制,因为更坚硬的 meDNA 更难以从核小体中去除。