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

AI Article Synopsis

  • The GGGGCC (G4C2) hexanucleotide repeat expansion in the C9orf72 gene is linked to amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) through toxic G-quadruplex formation.
  • Researchers have discovered a novel crystal structure of a d(G4C2)2 G-quadruplex that forms an eight-layered, parallel tetramer through self-association.
  • This study provides structural insights into G-quadruplexes, which could aid in the design of small molecules for treating ALS and FTD.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191786PMC
http://dx.doi.org/10.1093/nar/gkab302DOI Listing

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