# TOX High-Mobility Group Box Family Member 4 promotes DNA double-strand break repair via nonhomologous end joining

**Authors:** Feifei Wang, Wenli Gui, Mengtao Rong, Liang Zhang, Jiajing Wu, Juan Li, Renqing Wang, Odjo G. Gouttia, Ling Wang, Xingyuan Yang, Aimin Peng

PMC · DOI: 10.1016/j.jbc.2025.110174 · The Journal of Biological Chemistry · 2025-05-04

## TL;DR

TOX4 helps repair DNA breaks through a process called nonhomologous end joining, and its absence impairs DNA repair and could make cancer cells more vulnerable to treatment.

## Contribution

TOX4 is newly identified as a key factor in DNA repair via nonhomologous end joining by interacting with DNA-PK and phosphatase 1 nuclear-targeting subunit.

## Key findings

- TOX4 depletion leads to DNA damage accumulation and reduced nonhomologous end joining efficiency.
- TOX4 associates with DNA-PK and is required for DNA-PKcs activation.
- TOX4 coordinates with phosphatase 1 nuclear-targeting subunit to regulate DNA-PKcs phosphorylation.

## Abstract

Nonhomologous end joining (NHEJ) is a pivotal mechanism in the repair of DNA double-strand breaks. Central to NHEJ is the DNA-dependent protein kinase (DNA-PK) complex, comprising the KU heterodimer and the catalytic subunit, DNA-PKcs. In this study, we characterize Thymocyte Selection–Associated High-Mobility Group Box Family Member 4 (TOX4) as a factor recruited to both laser-induced DNA damage and endonuclease-induced DNA double-strand breaks. Depletion of TOX4 leads to accumulation of DNA damage, which is epistatic to DNA-PKcs. Consistently, TOX4 depletion substantially reduces NHEJ efficiency measured using both intrachromosomal and extrachromosomal repair assays. Our proteomic and biochemical analyses reveal TOX4 association with DNA-PK that is required for DNA-PKcs activation. Furthermore, we show that TOX4 coordinates with phosphatase 1 nuclear-targeting subunit in NHEJ. Phosphatase 1 nuclear-targeting subunit, previously shown to protect DNA-PKcs phosphorylation from protein phosphatase 1–mediated dephosphorylation, binds DNA-PK in a TOX4-dependent manner. In line with its role in DNA repair, TOX4 emerges as a promising target for anticancer drug development, and its targeting enhances tumor cell sensitivity to DNA damage in head and neck cancer and other malignancies.

## Linked entities

- **Genes:** TOX4 (TOX high mobility group box family member 4) [NCBI Gene 9878], PRKDC (protein kinase, DNA-activated, catalytic subunit) [NCBI Gene 5591], ku (non-homologous end joining protein Ku) [NCBI Gene 1136505]
- **Proteins:** TOX4 (TOX high mobility group box family member 4), PRKDC (protein kinase, DNA-activated, catalytic subunit), PRKDC (protein kinase, DNA-activated, catalytic subunit), ku (non-homologous end joining protein Ku)
- **Diseases:** head and neck cancer (MONDO:0005627)

## Full-text entities

- **Genes:** TOX4 (TOX high mobility group box family member 4) [NCBI Gene 9878] {aka C14orf92, KIAA0737, LCP1, MIG7}, PRKDC (protein kinase, DNA-activated, catalytic subunit) [NCBI Gene 5591] {aka DNA-PKC, DNA-PKcs, DNAPK, DNAPKc, DNPK1, HYRC}, PPP1R10 (protein phosphatase 1 regulatory subunit 10) [NCBI Gene 5514] {aka CAT53, FB19, PNUTS, PP1R10, R111, p99}, NPY4R (neuropeptide Y receptor Y4) [NCBI Gene 5540] {aka NPY4-R, PP1, PPYR1, Y4}
- **Diseases:** head and neck cancer (MESH:D006258), cancer (MESH:D009369)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12166427/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12166427/full.md

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Source: https://tomesphere.com/paper/PMC12166427