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高甲基化CPG岛DNA的光镊纳米测量法

Optical Trapping Nanometry of Hypermethylated CPG-Island DNA.

作者信息

Pongor Csaba I, Bianco Pasquale, Ferenczy György, Kellermayer Richárd, Kellermayer Miklós

机构信息

Biophysics and Radiation Biolology, Semmelweis University, Budapest, Hungary.

Biophysics and Radiation Biolology, Semmelweis University, Budapest, Hungary; Physiolab, Department of Biology, University of Florence, Sesto Fiorentino (FI), Italy.

出版信息

Biophys J. 2017 Feb 7;112(3):512-522. doi: 10.1016/j.bpj.2016.12.029. Epub 2017 Jan 18.

Abstract

Cytosine methylation is a key mechanism of epigenetic regulation. CpG-dense loci, called "CpG islands", play a particularly important role in modulating gene expression. Methylation has long been suspected to alter the physical properties of DNA, but the full spectrum of the evoked changes is unknown. Here we measured the methylation-induced nanomechanical changes in a DNA molecule with the sequence of a CpG island. For the molecule under tension, contour length, bending rigidity and intrinsic stiffness decreased in hypermethylated dsDNA, pointing at structural compaction which may facilitate DNA packaging in vivo. Intriguingly, increased forces were required to convert hypermethylated dsDNA into an extended S-form configuration. The reduction of force hysteresis during mechanical relaxation indicated that methylation generates a barrier against strand unpeeling and melting-bubble formation. The high structural stability is likely to have significant consequences on the recognition, replication, transcription, and reparation of hypermethylated genetic regions.

摘要

胞嘧啶甲基化是表观遗传调控的关键机制。富含CpG的位点,即所谓的“CpG岛”,在调节基因表达中起着特别重要的作用。长期以来,人们一直怀疑甲基化会改变DNA的物理性质,但所引发变化的全貌尚不清楚。在这里,我们测量了具有CpG岛序列的DNA分子中甲基化诱导的纳米力学变化。对于处于张力下的分子,超甲基化双链DNA的轮廓长度、弯曲刚度和固有刚度降低,表明结构紧凑,这可能有助于体内DNA的包装。有趣的是,将超甲基化双链DNA转化为延伸的S形构象需要更大的力。机械弛豫过程中力滞后的减少表明甲基化产生了阻碍链解旋和熔泡形成的屏障。这种高结构稳定性可能对超甲基化基因区域的识别、复制、转录和修复产生重大影响。

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