Optical control of gene expression using a DNA G-quadruplex targeting reversible photoswitch

Transcriptional regulation is a dynamic process that coordinates diverse cellular activities, and the use of small molecules to perturb gene expression has propelled our understanding of the fundamental regulatory mechanisms. However, small molecules typically lack the spatiotemporal precision required in highly non-invasive, controlled settings. Here we present the development of a cell-permeable small-molecule DNA G-quadruplex (G4) binder, termed G4switch, that can be reversibly toggled on and off by visible light. We have biophysically characterized the light-mediated control of G4 binding in vitro, followed by cellular, genomic mapping of G4switch to G4 targets in chromatin to confirm G4-selective, light-dependent binding in a cellular context. By deploying G4switch in living cells, we show spatiotemporal control over the expression of a set of G4-containing genes and G4-associated cell proliferation. Our studies demonstrate a chemical tool and approach to interrogate the dynamics of key biological processes directly at the molecular level in cells.

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Publication Details

Journal
Nature Chemistry
Published
2025-04-03
DOI
https://doi.org/10.1038/s41557-025-01792-1
Citations
13
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
10.48

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article

Optical control of gene expression using a DNA G-quadruplex targeting reversible photoswitch

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13 citations
Nature Chemistry
Advanced biosensing and bioanalysis techniques
10.48
article

Optical control of gene expression using a DNA G-quadruplex targeting reversible photoswitch

Somdutta Dhir, Jochen Spiegel, Larry Melidis, Angela Simeone, Santosh Adhikari, Shankar Balasubramanian, Zutao Yu, Xiaoyun Zhang, Yuqi Chen
article en
13 citations

Abstract

Transcriptional regulation is a dynamic process that coordinates diverse cellular activities, and the use of small molecules to perturb gene expression has propelled our understanding of the fundamental regulatory mechanisms. However, small molecules typically lack the spatiotemporal precision required in highly non-invasive, controlled settings. Here we present the development of a cell-permeable small-molecule DNA G-quadruplex (G4) binder, termed G4switch, that can be reversibly toggled on and off by visible light. We have biophysically characterized the light-mediated control of G4 binding in vitro, followed by cellular, genomic mapping of G4switch to G4 targets in chromatin to confirm G4-selective, light-dependent binding in a cellular context. By deploying G4switch in living cells, we show spatiotemporal control over the expression of a set of G4-containing genes and G4-associated cell proliferation. Our studies demonstrate a chemical tool and approach to interrogate the dynamics of key biological processes directly at the molecular level in cells.

Nature ChemistryVol. 17(6)
University of Cambridge (GB), Cancer Research UK (GB), Cancer Research UK Cambridge Center (GB), Cambridge School (PT)
Wellcome, Wellcome Trust, Cancer Research UK, Cancer Research UK Cambridge Institute, University of Cambridge
Openalex Percentile: Top 1%
Advanced biosensing and bioanalysis techniques
10.48
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