# Carboxymethylcytosine is a natural base modification and a handle for bacteriophage DNA hypermodification

**Authors:** Qiaoyu Yang, Lin Zhang, Yantao Liang, Haoyu Ma, Lifu Song, Lin Luo, Jason Tan, Yiling Hu, Kailiang Ma, Yiwei Chen, Yang Tong, Chuyuan Zhang, Suwen Zhao, Min Wang, Liang Zhang, Yifeng Wei, Yan Zhang

PMC · DOI: 10.1038/s41467-025-66999-9 · Nature Communications · 2025-12-07

## TL;DR

This paper shows that carboxymethylcytosine is a natural DNA modification in bacteriophages and helps enable further DNA changes.

## Contribution

The discovery that carboxymethylcytosine is a natural DNA base and its role in phage DNA hypermodification.

## Key findings

- CmoX catalyzes the formation of 5-carboxymethylcytosine in bacteriophage DNA.
- CmoA and CmoY are involved in producing and modifying 5cxmC in phages.
- 5cxmC modification is widespread in phage genomes and supports further hypermodifications.

## Abstract

Bacteriophages possess a wide array of DNA modifications, with many acting as molecular camouflage to evade host immune defenses. Sequence databases contain numerous bacteriophage enzymes of unknown function, with some potentially involved in yet to be identified DNA modifications. Here we report the discovery of a DNA cytosine C5-carboxymethyltransferase (CmoX) in Synechococcus phage S-B43, which catalyzes the formation of a 5-carboxymethylcytosine (5cxmC), previously reported as an unnatural DNA modification formed by an engineered cytosine methyltransferase. The carboxy-S-adenosyl-L-methionine (Cx-SAM) cofactor required by CmoX is provided by a phage-encoded Cx-SAM synthase (CmoA), a homolog of the bacterial CmoA involved in tRNA modification. A crystal structure of CmoX in complex with Cx-SAM revealed the basis for its substrate selectivity, involving a key Arg residue interacting with the substrate carboxy group. In addition, we characterize a phage-encoded ATP-dependent amide ligase, CmoY that catalyzes the formation of 5cxmC-glycine amide. CmoA is present in many bacteriophage genomes, typically alongside CmoX and homologs of CmoY, suggesting that 5cxmC modification is a widespread naturally occurring DNA modification serving as a handle for further hypermodifications in bacteriophages. Our study underscores the ability of bacteriophages to repurpose RNA modification enzymes to expand their repertoire of DNA modifications.

DNA in many bacteriophages contains unusual chemical modifications. Here, the authors discover that carboxymethylcytosine is a natural DNA base and reveal its role as an intermediate enabling further DNA hypermodification.

## Linked entities

- **Genes:** cmoA (carboxy-SAM synthase) [NCBI Gene 912510]
- **Proteins:** cmoA (carboxy-SAM synthase)
- **Chemicals:** 5-carboxymethylcytosine (PubChem CID 22079961), carboxy-S-adenosyl-L-methionine (PubChem CID 11212932)
- **Species:** Synechococcus phage S-B43 (taxon 2484638)

## Full-text entities

- **Chemicals:** 5-carboxymethylcytosine (-)
- **Species:** Bacteriophage sp. (species) [taxon 38018]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12783734/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12783734/full.md

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Source: https://tomesphere.com/paper/PMC12783734