Ngo Thuy T M, Yoo Jejoong, Dai Qing, Zhang Qiucen, He Chuan, Aksimentiev Aleksei, Ha Taekjip
Center for Biophysics and Quantitative Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Department of Physics and Center for the Physics of Living Cells, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Nat Commun. 2016 Feb 24;7:10813. doi: 10.1038/ncomms10813.
Cytosine can undergo modifications, forming 5-methylcytosine (5-mC) and its oxidized products 5-hydroxymethylcytosine (5-hmC), 5-formylcytosine (5-fC) and 5-carboxylcytosine (5-caC). Despite their importance as epigenetic markers and as central players in cellular processes, it is not well understood how these modifications influence physical properties of DNA and chromatin. Here we report a comprehensive survey of the effect of cytosine modifications on DNA flexibility. We find that even a single copy of 5-fC increases DNA flexibility markedly. 5-mC reduces and 5-hmC enhances flexibility, and 5-caC does not have a measurable effect. Molecular dynamics simulations show that these modifications promote or dampen structural fluctuations, likely through competing effects of base polarity and steric hindrance, without changing the average structure. The increase in DNA flexibility increases the mechanical stability of the nucleosome and vice versa, suggesting a gene regulation mechanism where cytosine modifications change the accessibility of nucleosomal DNA through their effects on DNA flexibility.
胞嘧啶可发生修饰,形成5-甲基胞嘧啶(5-mC)及其氧化产物5-羟甲基胞嘧啶(5-hmC)、5-甲酰基胞嘧啶(5-fC)和5-羧基胞嘧啶(5-caC)。尽管它们作为表观遗传标记以及细胞过程中的核心参与者很重要,但人们对这些修饰如何影响DNA和染色质的物理性质却了解甚少。在此,我们报告了对胞嘧啶修饰对DNA柔韧性影响的全面研究。我们发现,即使是单个拷贝的5-fC也会显著增加DNA的柔韧性。5-mC降低柔韧性,5-hmC增强柔韧性,而5-caC没有可测量的影响。分子动力学模拟表明,这些修饰通过碱基极性和空间位阻的竞争效应促进或抑制结构波动,而不改变平均结构。DNA柔韧性的增加会增加核小体的机械稳定性,反之亦然,这表明存在一种基因调控机制,其中胞嘧啶修饰通过影响DNA柔韧性来改变核小体DNA的可及性。