posted on 2024-02-06, 16:40authored byLiqi Wan, Axin He, Jinxing Li, Pei Guo, Da Han
The CAG and CTG trinucleotide repeat expansions cause
more than
10 human neurodegenerative diseases. Intrastrand hairpins formed by
trinucleotide repeats contribute to repeat expansions, establishing
them as potential drug targets. High-resolution structural determination
of CAG and CTG hairpins poses as a long-standing goal to aid drug
development, yet it has not been realized due to the intrinsic conformational
flexibility of repetitive sequences. We herein investigate the solution
structures of CTG hairpins using nuclear magnetic resonance (NMR)
spectroscopy and found that four CTG repeats with a clamping G-C base
pair was able to form a stable hairpin structure. We determine the
first solution NMR structure of dG(CTG)4C hairpin and decipher
a type I folding geometry of the TGCT tetraloop, wherein the two thymine
residues form a T·T loop-closing base pair and the first three
loop residues continuously stack. We further reveal that the CTG hairpin
can be bound and stabilized by a small-molecule ligand, and the binding
interferes with replication of a DNA template containing CTG repeats.
Our determined high-resolution structures lay an important foundation
for studying molecular interactions between native CTG hairpins and
ligands,
and benefit drug development for trinucleotide repeat expansion diseases.