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两重复制 ALS 和 FTD 相关 GGGGCC 序列形成的平行 G-四链体的晶体结构。

Crystal structure of parallel G-quadruplex formed by the two-repeat ALS- and FTD-related GGGGCC sequence.

机构信息

Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, 00000, China.

Institute of Molecular Enzymology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, Jiangsu, 215123, China.

出版信息

Nucleic Acids Res. 2021 Jun 4;49(10):5881-5890. doi: 10.1093/nar/gkab302.

Abstract

The hexanucleotide repeat expansion, GGGGCC (G4C2), within the first intron of the C9orf72 gene is known to be the most common genetic cause of both amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). The G4C2 repeat expansions, either DNA or RNA, are able to form G-quadruplexes which induce toxicity leading to ALS/FTD. Herein, we report a novel crystal structure of d(G4C2)2 that self-associates to form an eight-layer parallel tetrameric G-quadruplex. Two d(G4C2)2 associate together as a parallel dimeric G-quadruplex which folds into a tetramer via 5'-to-5' arrangements. Each dimer consists of four G-tetrads connected by two CC propeller loops. Especially, the 3'-end cytosines protrude out and form C·C+•C·C+/ C·C•C·C+ quadruple base pair or C•C·C+ triple base pair stacking on the dimeric block. Our work sheds light on the G-quadruplexes adopted by d(G4C2) and yields the invaluable structural details for the development of small molecules to tackle neurodegenerative diseases, ALS and FTD.

摘要

位于 C9orf72 基因第一个内含子中的六核苷酸重复扩增 GGGGCC(G4C2)已知是肌萎缩侧索硬化症(ALS)和额颞叶痴呆(FTD)的最常见遗传原因。无论是 DNA 还是 RNA 的 G4C2 重复扩增都能够形成 G-四链体,从而导致 ALS/FTD 毒性。在此,我们报告了 d(G4C2)2 的一种新型晶体结构,该结构能够自我组装形成八层平行四聚体 G-四链体。两个 d(G4C2)2 作为平行二聚体 G-四链体相互结合,然后通过 5'-到-5'排列折叠成四聚体。每个二聚体由四个 G-四联体组成,由两个 CC 推进器环连接。特别是,3'-末端胞嘧啶突出并形成 C·C+•C·C+/ C·C•C·C+四重碱基对或 C·C·C+三重碱基对堆积在二聚体块上。我们的工作阐明了 d(G4C2) 采用的 G-四链体,并为开发小分子以应对神经退行性疾病、ALS 和 FTD 提供了宝贵的结构细节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c2d/8191786/72f3ad921605/gkab302fig1.jpg

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