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Crystal structure of parallel G-quadruplex formed by the two-repeat ALS- and FTD-related GGGGCC sequence
Author(s) -
Yanyan Geng,
Changdong Liu,
Qixu Cai,
Zhipu Luo,
Haitao Miao,
Shi Xiao,
Naining Xu,
Chun Po Fung,
To To Choy,
Bing Yan,
Ning Li,
PeiYuan Qian,
Bo Zhou,
Guang Zhu
Publication year - 2021
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkab302
Subject(s) - c9orf72 , biology , stacking , trinucleotide repeat expansion , frontotemporal dementia , base pair , intron , dimer , sequence (biology) , genetics , g quadruplex , stereochemistry , gene , dna , chemistry , physics , medicine , dementia , nuclear magnetic resonance , allele , disease , pathology
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.

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