# Thymine DNA glycosylase binds to R-loops and excises 5-formyl and 5-carboxyl cytosine from DNA/RNA hybrids

**Authors:** Baiyu Zhu, Lakshmi S. Pidugu, Mary E. Cook, Xinyu Y. Nie, E.A.P. Tharaka Amarasekara, Jerome S. Menet, Alexander C. Drohat, Jonathan T. Sczepanski

PMC · DOI: 10.1016/j.jbc.2026.111308 · The Journal of Biological Chemistry · 2026-02-26

## TL;DR

This study shows that TDG can bind to R-loops and remove specific modified cytosines from DNA/RNA hybrids, suggesting a role in DNA demethylation.

## Contribution

The study demonstrates TDG's ability to excise 5fC and 5caC from DNA/RNA hybrids and provides mechanistic insights into R-loop-mediated DNA demethylation.

## Key findings

- TDG binds to R-loop substrates and excises 5fC and 5caC from DNA/RNA hybrids.
- R-loops enable strand-specific TDG activity at CpGs, explaining asymmetric 5fC/5caC distribution.
- 19F NMR reveals mechanistic details of base excision in DNA/RNA hybrid duplexes.

## Abstract

Once considered rare byproducts of transcription, R-loops are now recognized as important regulators of various nuclear processes. In particular, evidence indicates a role for R-loops in regulating DNA methylation dynamics. R-loops have been shown to promote active DNA demethylation—the enzymatic reversal of 5-methylcytosine back into cytosine—by recruiting associated proteins, providing an attractive targeting mechanism. Nevertheless, many aspects of this process, including whether the associated proteins bind to and function on DNA within R-loops, remain to be substantiated. Herein, we demonstrate that thymine DNA glycosylase (TDG), a key enzyme in the active DNA demethylation pathway, binds to synthetic R-loop substrates in vitro and can excise DNA demethylation intermediates 5-formylcytosine (5fC) and 5-carboxycytosine (5caC) from DNA in DNA/RNA hybrids. We also show that R-loops confer strand-specific TDG activity at CpGs, potentially explaining the asymmetric distribution of 5fC/5caC at gene promoters. Furthermore, we provide important mechanistic insights into base excision on DNA/RNA hybrid duplexes using 19F NMR. Finally, our findings raise the possibility that TDG–R-loop interactions could occur in mammalian cells. Collectively, our results establish a biochemical mechanism by which 5fC/5caC can be removed from DNA within DNA/RNA hybrids, which has important implication for the role of R-loops during DNA demethylation.

## Linked entities

- **Proteins:** TDG (thymine DNA glycosylase)
- **Chemicals:** 5-formylcytosine (PubChem CID 10986305), 5fC (PubChem CID 3366), 5-carboxycytosine (PubChem CID 77213), 5-methylcytosine (PubChem CID 65040)

## Full-text entities

- **Genes:** TDG (thymine DNA glycosylase) [NCBI Gene 6996] {aka hTDG}
- **Chemicals:** 5-Formyl (-), 5-formylcytosine (MESH:C560973), 5-Carboxyl Cytosine (MESH:C560974), cytosine (MESH:D003596), 5-methylcytosine (MESH:D044503), 5-carboxycytosine (MESH:C000618843)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13022674/full.md

## References

92 references — full list in the complete paper: https://tomesphere.com/paper/PMC13022674/full.md

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Source: https://tomesphere.com/paper/PMC13022674