Beyond small molecules: targeting G-quadruplex structures with oligonucleotides and their analogues

Author:

Cadoni Enrico1,De Paepe Lessandro1,Manicardi Alex1,Madder Annemieke1

Affiliation:

1. Organic and Biomimetic Chemistry Research Group, Ghent University, Krijgslaan 281 S4, B-9000 Ghent, Belgium

Abstract

Abstract G-Quadruplexes (G4s) are widely studied secondary DNA/RNA structures, naturally occurring when G-rich sequences are present. The strategic localization of G4s in genome areas of crucial importance, such as proto-oncogenes and telomeres, entails fundamental implications in terms of gene expression regulation and other important biological processes. Although thousands of small molecules capable to induce G4 stabilization have been reported over the past 20 years, approaches based on the hybridization of a synthetic probe, allowing sequence-specific G4-recognition and targeting are still rather limited. In this review, after introducing important general notions about G4s, we aim to list, explain and critically analyse in more detail the principal approaches available to target G4s by using oligonucleotides and synthetic analogues such as Locked Nucleic Acids (LNAs) and Peptide Nucleic Acids (PNAs), reporting on the most relevant examples described in literature to date.

Funder

European Union's Horizon 2020 research and innovation programme

Marie Skłodowska-Curie Actions

UGent Industrieel OnderzoeksFonds

ITN Oligomed

Publisher

Oxford University Press (OUP)

Subject

Genetics

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