Carvalho Alexandra T P, Gouveia Leonor, Kanna Charan Raju, Wärmländer Sebastian K T S, Platts Jamie A, Kamerlin Shina Caroline Lynn
a Science for Life Laboratory; Department of Cell and Molecular Biology ; Uppsala University ; Uppsala , Sweden.
Epigenetics. 2014 Dec;9(12):1604-12. doi: 10.4161/15592294.2014.988043.
We report a series of molecular dynamics (MD) simulations of up to a microsecond combined simulation time designed to probe epigenetically modified DNA sequences. More specifically, by monitoring the effects of methylation and hydroxymethylation of cytosine in different DNA sequences, we show, for the first time, that DNA epigenetic modifications change the molecule's dynamical landscape, increasing the propensity of DNA toward different values of twist and/or roll/tilt angles (in relation to the unmodified DNA) at the modification sites. Moreover, both the extent and position of different modifications have significant effects on the amount of structural variation observed. We propose that these conformational differences, which are dependent on the sequence environment, can provide specificity for protein binding.
我们报告了一系列分子动力学(MD)模拟,总模拟时间长达微秒,旨在探究表观遗传修饰的DNA序列。更具体地说,通过监测不同DNA序列中胞嘧啶甲基化和羟甲基化的影响,我们首次表明,DNA表观遗传修饰改变了分子的动力学格局,增加了修饰位点处DNA相对于未修饰DNA呈现不同扭转和/或滚动/倾斜角度值的倾向。此外,不同修饰的程度和位置对观察到的结构变化量有显著影响。我们提出,这些依赖于序列环境的构象差异可为蛋白质结合提供特异性。