Harris, LM, Monsell, KM, Noulin, F, Famodimu, MT, Smargiasso, N, Damblon, C, Horrocks, P ORCID: https://orcid.org/0000-0003-3981-0732 and Merrick, CJ (2018) G-quadruplex DNA motifs in the malaria parasite Plasmodium falciparum and their potential as novel antimalarial drug targets. Antimicrobial Agents and Chemotherapy, 62 (3).

[img]
Preview
Text
AAC01828-17R1_Merged_PDF.pdf - Accepted Version
Available under License Creative Commons Attribution Non-commercial.

Download (2MB) | Preview

Abstract

G-quadruplexes are DNA or RNA secondary structures that can be formed from guanine-rich nucleic acids. These four-stranded structures, composed of stacked quartets of guanine bases, can be highly stable and have been demonstrated to occur in vivo in the DNA of human cells and other systems, where they play important biological roles, influencing processes such as telomere maintenance, DNA replication and transcription, or, in the case of RNA G-quadruplexes, RNA translation and processing. We report for the first time that DNA G-quadruplexes can be detected in the nuclei of the malaria parasite Plasmodium falciparum, which has one of the most A/T-biased genomes sequenced and therefore possesses few guanine-rich sequences with the potential to form G-quadruplexes. We show that despite this paucity of putative G-quadruplex-forming sequences, P. falciparum parasites are sensitive to several G-quadruplex-stabilizing drugs, including quarfloxin, which previously reached phase 2 clinical trials as an anticancer drug. Quarfloxin has a rapid initial rate of kill and is active against ring stages as well as replicative stages of intraerythrocytic development. We show that several G-quadruplex-stabilizing drugs, including quarfloxin, can suppress the transcription of a G-quadruplex-containing reporter gene in P. falciparum but that quarfloxin does not appear to disrupt the transcription of rRNAs, which was proposed as its mode of action in both human cells and trypanosomes. These data suggest that quarfloxin has potential for repositioning as an antimalarial with a novel mode of action. Furthermore, G-quadruplex biology in P. falciparum may present a target for development of other new antimalarial drugs.

Item Type: Article
Additional Information: This is the accepted author manuscript (AAM). The final published version (version of record) is available online via ASM at http://dx.doi.org/10.1128/AAC.01828-17 - please refer to any applicable terms of use of the publisher.
Uncontrolled Keywords: Malaria, Plasmodium falciparum, G-quadruplex, Quarfloxin
Subjects: Q Science > Q Science (General)
Q Science > QH Natural history
Divisions: Faculty of Natural Sciences > School of Life Sciences
Depositing User: Symplectic
Date Deposited: 11 Jan 2018 08:47
Last Modified: 01 Apr 2019 10:06
URI: http://eprints.keele.ac.uk/id/eprint/4346

Actions (login required)

View Item View Item