» Articles » PMID: 30591567

DNA Damage and Genome Instability by G-quadruplex Ligands Are Mediated by R Loops in Human Cancer Cells

Overview
Specialty Science
Date 2018 Dec 29
PMID 30591567
Citations 149
Authors
Affiliations
Soon will be listed here.
Abstract

G quadruplexes (G4s) and R loops are noncanonical DNA structures that can regulate basic nuclear processes and trigger DNA damage, genome instability, and cell killing. By different technical approaches, we here establish that specific G4 ligands stabilize G4s and simultaneously increase R-loop levels within minutes in human cancer cells. Genome-wide mapping of R loops showed that the studied G4 ligands likely cause the spreading of R loops to adjacent regions containing G4 structures, preferentially at 3'-end regions of expressed genes, which are partially ligand-specific. Overexpression of an exogenous human RNaseH1 rescued DNA damage induced by G4 ligands in -proficient and -silenced cancer cells. Moreover, even if the studied G4 ligands increased noncanonical DNA structures at similar levels in nuclear chromatin, their cellular effects were different in relation to cell-killing activity and stimulation of micronuclei, a hallmark of genome instability. Our findings therefore establish that G4 ligands can induce DNA damage by an R loop-dependent mechanism that can eventually lead to different cellular consequences depending on the chemical nature of the ligands.

Citing Articles

The G-quadruplex experimental drug QN-302 impairs liposarcoma cell growth by inhibiting MDM2 expression and restoring p53 levels.

Tosoni B, Naghshineh E, Zanin I, Gallina I, Di Pietro L, Cleris L Nucleic Acids Res. 2025; 53(4).

PMID: 39945321 PMC: 11822379. DOI: 10.1093/nar/gkaf085.


Gene regulation by convergent promoters.

Wiechens E, Vigliotti F, Siniuk K, Schwarz R, Schwab K, Riege K Nat Genet. 2025; 57(1):206-217.

PMID: 39779959 PMC: 11735407. DOI: 10.1038/s41588-024-02025-w.


Nuclear microRNA 9 mediates G-quadruplex formation and 3D genome organization during TGF-β-induced transcription.

Cordero J, Swaminathan G, Rogel-Ayala D, Rubio K, Elsherbiny A, Mahmood S Nat Commun. 2024; 15(1):10711.

PMID: 39706840 PMC: 11662019. DOI: 10.1038/s41467-024-54740-x.


The hidden architects of the genome: a comprehensive review of R-loops.

Yadav C, Yadav R, Nanda S, Ranga S, Ahuja P Mol Biol Rep. 2024; 51(1):1095.

PMID: 39460836 DOI: 10.1007/s11033-024-10025-6.


The Smc5/6 complex counteracts R-loop formation at highly transcribed genes in cooperation with RNase H2.

Roy S, Adhikary H, Isler S, DAmours D Elife. 2024; 13.

PMID: 39404251 PMC: 11620742. DOI: 10.7554/eLife.96626.


References
1.
Sollier J, Cimprich K . Breaking bad: R-loops and genome integrity. Trends Cell Biol. 2015; 25(9):514-22. PMC: 4554970. DOI: 10.1016/j.tcb.2015.05.003. View

2.
Yadav P, Harcy V, Argueso J, Dominska M, Jinks-Robertson S, Kim N . Topoisomerase I plays a critical role in suppressing genome instability at a highly transcribed G-quadruplex-forming sequence. PLoS Genet. 2014; 10(12):e1004839. PMC: 4256205. DOI: 10.1371/journal.pgen.1004839. View

3.
Skourti-Stathaki K, Proudfoot N . A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression. Genes Dev. 2014; 28(13):1384-96. PMC: 4083084. DOI: 10.1101/gad.242990.114. View

4.
Skourti-Stathaki K, Proudfoot N, Gromak N . Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination. Mol Cell. 2011; 42(6):794-805. PMC: 3145960. DOI: 10.1016/j.molcel.2011.04.026. View

5.
Sanz L, Hartono S, Lim Y, Steyaert S, Rajpurkar A, Ginno P . Prevalent, Dynamic, and Conserved R-Loop Structures Associate with Specific Epigenomic Signatures in Mammals. Mol Cell. 2016; 63(1):167-78. PMC: 4955522. DOI: 10.1016/j.molcel.2016.05.032. View