Bie Lihua, Du Likai, Yuan Qiaoxia, Gao Jun
Agricultural Bioinformatics Key Laboratory of Hubei Province, College of Informatics, Huazhong Agricultural University, Wuhan, 430070, People's Republic of China.
College of Engineering, Huazhong Agricultural University, Wuhan, 430070, People's Republic of China.
J Mol Model. 2018 Jun 11;24(7):159. doi: 10.1007/s00894-018-3678-8.
CpG methylation can regulate gene expression by altering the specific binding of protein and DNA. In order to understand how a single 5mC regulates protein-DNA interactions, we have compared the structures and dynamics of CEBP/βprotein-DNA complexes before and after methylation, and the results indicate that even a single 5mC can regulate protein-DNA recognition by steric-hindrance effect of methyl group and changing the hydrogen bond interactions. The interactions between the methyl group, mCpG motif, and the conserved residue arginine make the protein read out the variation of local environment, which further enhances the specific recognition and affects the base pair stacking. The stacking interactions can propagate along the backbone of DNA and lead to long-range allosteric effects, including obvious conformational variations for DNA base pairs.
CpG甲基化可通过改变蛋白质与DNA的特异性结合来调节基因表达。为了了解单个5-甲基胞嘧啶(5mC)如何调节蛋白质-DNA相互作用,我们比较了甲基化前后CEBP/β蛋白-DNA复合物的结构和动力学,结果表明,即使是单个5mC也可通过甲基基团的空间位阻效应和改变氢键相互作用来调节蛋白质-DNA识别。甲基基团、mCpG基序和保守残基精氨酸之间的相互作用使蛋白质能够读出局部环境的变化,进而增强特异性识别并影响碱基对堆积。堆积相互作用可沿DNA主链传播并导致长程变构效应,包括DNA碱基对明显的构象变化。