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胞嘧啶甲基化在调节DNA G-四链体的拓扑结构和液-液相分离中的作用。

The role of cytosine methylation in regulating the topology and liquid-liquid phase separation of DNA G-quadruplexes.

作者信息

Tsuruta Mitsuki, Shil Sumit, Taniguchi Shinya, Kawauchi Keiko, Miyoshi Daisuke

机构信息

Faculty of Frontiers of Innovative Research in Science and Technology (FIRST), Konan University 7-1-20 Minatojima-minamimachi, Chuo-ku Kobe Hyogo 650-0047 Japan

出版信息

Chem Sci. 2025 Jan 31;16(10):4213-4225. doi: 10.1039/d4sc06959e. eCollection 2025 Mar 5.

Abstract

Aberrant expansion of GGGGCC DNA repeats that form G-quadruplexes (G4) is the main cause of amyotrophic lateral sclerosis (ALS). Expanded GGGGCC repeats induce liquid-liquid phase separation (LLPS) through their interaction with cellular proteins. Furthermore, GGGGCC expansion induces cytosine methylation (mC). Previous studies have shown that even slight chemical modifications of RNAs and proteins can drastically affect their LLPS ability, yet the relationship between LLPS and epigenetic DNA modifications like mC remains unexplored. As a model system, we investigated the effects of mC on LLPS induced by GGGGCC repeat DNAs and show for the first time that mC suppresses LLPS by altering the topology of G4 from being parallel to antiparallel.

摘要

形成G-四链体(G4)的GGGGCC DNA重复序列的异常扩增是肌萎缩侧索硬化症(ALS)的主要病因。扩增的GGGGCC重复序列通过与细胞蛋白相互作用诱导液-液相分离(LLPS)。此外,GGGGCC扩增会诱导胞嘧啶甲基化(mC)。先前的研究表明,即使RNA和蛋白质发生轻微的化学修饰也会极大地影响它们的LLPS能力,然而LLPS与mC等表观遗传DNA修饰之间的关系仍未得到探索。作为一个模型系统,我们研究了mC对GGGGCC重复DNA诱导的LLPS的影响,并首次表明mC通过将G4的拓扑结构从平行改变为反平行来抑制LLPS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cd8/11881068/e23831a50201/d4sc06959e-f1.jpg

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