PLoS ONE · 2018 · 14 citations · 40 references
Life SciencesBiochemistryMolecular BiologyGenomicsNeurodegenerationStructural BiologyDna StructureMolecular Basis Of NeurodegenerationNeurodegenerative DiseasesNeurodegenerative DisordersNucleic Acid StructureStructural MotifsC9orf72 Repeat ExpansionCircular DichroismDna Double HelixG-quadruplex RepeatsG-quadruplex StructureG-quadruplexesQuadruplex Base PairingTriplex Dna
Massive expansion of a DNA hexanucleotide sequence repeat (C2G4) within the human C9orf72 gene has been linked to a number of neurodegenerative diseases. In sodium or potassium salt solutions, single-stranded d(C2G4)n DNAs fold to form G-quadruplexes. We have found that in magnesium or lithium salt solutions, especially under slightly acidic conditions, d(C2G4)n oligonucleotides fold to form a distinctive higher order structure whose most striking feature is an "inverted" circular dichroism spectrum, which is distinguishable from the spectrum of the left handed DNA double-helix, Z-DNA. On the basis of CD spectroscopy, gel mobility as well as chemical protection analysis, we propose that this structure, which we call "iCD-DNA", may be a left-handed Hoogsteen base-paired duplex, an unorthodox G-quadruplex/i-motif composite, or a non-canonical, "braided" DNA triplex. Given that iCD-DNA forms under slightly acidic solution conditions, we do not know at this point in time whether or not it forms within living cells.
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A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
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Life Sciences, Genetics, Neurology +17
RNA phase transitions in repeat expansion disorders
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