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. 2023 Jan 13;14:205. doi: 10.1038/s41467-023-35811-x

Fig. 4. 3′ UTR RNA G-quadruplex folding enhances mRNA stability under stress and such folding is reversible.

Fig. 4

a U2OS cells were actinomycin-D treated over an indicated period of time and the relative abundance of specific mRNA was analyzed. RT-qPCR quantification showed 3'UTR rG4 bearing mRNAs are significantly more stable under starvation stress, data are presented as mean values + /− SD, n = 3, Multiple paired t-tests, p-values are provided when p > 0.05. b Comparative mRNA stability in the presence of rG4 stabilizing ligands (cPDS and BRACO-19) showed a similar trend in mRNA stability as observed under starvation conditions, data are presented as mean values + /− SD, n = 3, ordinary One-way ANOVA, Multiple comparisons, adjusted p-values are provided when p > 0.05. c rG4 folding is reversible upon stress removal (also Supplementary Fig. S9) and such reversibility can be largely paused by rG4 stabilizing ligand cPDS, along with nutrient stresses created by 2-DG (glycolysis inhibitor) and CCCP (oxidative phosphorylation inhibitor) treatment. d Quantification of BG4 fluorescence from 10 cells per conditions in c and Supplementary Fig. S9, the experiment was performed in biological triplicate, the data presented as mean values + /− SD. Ordinary One-way ANOVA, Multiple comparisons, p-values are provided when p > 0.05, and e proposed model to demonstrate the dynamic nature of stress-responsive rG4 folding and their contribution to mRNA stability.