High-Resolution NMR Structures of Intrastrand Hairpins Formed by CTG Trinucleotide Repeats.

ACS Chem Neurosci

Institute of Molecular Medicine (IMM), Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.

Published: February 2024


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

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)C 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.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acschemneuro.3c00769DOI Listing

Publication Analysis

Top Keywords

ctg hairpins
12
intrastrand hairpins
8
hairpins formed
8
ctg
8
ctg trinucleotide
8
trinucleotide repeats
8
cag ctg
8
trinucleotide repeat
8
repeat expansions
8
drug development
8

Similar Publications

Hairpin-forming CAG/CTG repeats pose significant challenges to DNA replication. In S. cerevisiae, long CAG/CTG repeat tracts reposition from the interior of the nucleus to the nuclear pore complex (NPC) to maintain their integrity.

View Article and Find Full Text PDF

CAG/CTG repeats are prone to expansion, causing several inherited human diseases. The initiating sources of DNA damage which lead to inaccurate repair of the repeat tract to cause expansions are not fully understood. Expansion-prone CAG/CTG repeats are actively transcribed and prone to forming stable R-loops with hairpin structures forming on the displaced single-stranded DNA (S-loops).

View Article and Find Full Text PDF

The packaging signal of Xanthomonas integrative filamentous phages.

Virology

December 2024

Agricultural Biotechnology Laboratory, Auxergen Inc., Riti Rossi Colwell Center, 701 E Pratt Street, Baltimore, MD 21202, USA; Auxergen S.r.l., Tecnopolis Science and Tecnopolis Park of the University of Bari, Valenzano, BA, Italy.

Unlike Ff, the packaging signal (PS) and the mechanism of integrative filamentous phage assembly remains largely unknown. Here we revived two Inoviridae prophage sequences, ϕLf2 and ϕLf-UK, as infectious virions that lysogenize black rot pathogen Xanthomonas campestris pv. campestris.

View Article and Find Full Text PDF

Dynamic mutations in some human genes containing trinucleotide repeats are associated with severe neurodegenerative and neuromuscular disorders-known as Trinucleotide (or Triplet) Repeat Expansion Diseases (TREDs)-which arise when the repeat number of triplets expands beyond a critical threshold. While the mechanisms causing the DNA triplet expansion are complex and remain largely unknown, it is now recognized that the expandable repeats lead to the formation of nucleotide configurations with atypical structural characteristics that play a crucial role in TREDs. These nonstandard nucleic acid forms include single-stranded hairpins, Z-DNA, triplex structures, G-quartets and slipped-stranded duplexes.

View Article and Find Full Text PDF
Article Synopsis
  • - Myotonic dystrophy type 1 (DM1) is caused by a CTG triplet repeat expansion that leads to the production of RNA with excessive CUG repeats, which accumulate and form structures in cell nuclei; the mechanisms behind their expression and accumulation aren't fully understood.
  • - Researchers discovered that HSP90 plays a crucial role in modifying RNA foci levels in DM1 cells, with its inhibition leading to increased RNA foci and mRNA levels, supported by experiments where HSP90 was either knocked down or overexpressed.
  • - In differentiated DM1 cells, HSP90 inhibition caused a decrease in mRNA levels through a mechanism that doesn't involve p-STAT3, highlighting the complexity of HSP90's role
View Article and Find Full Text PDF