Evidence map›Paper›PMID 42055551›Full record

ArticleNucleic acids research2026

HSF1 and YTHDC1 enhance DNA repair under heat stress by promoting repair-associated gene expression.

Wenqing Ding, Qidong Deng, Tianyu Wang, Ruoqian Liu, Yunfan Xiang, Lulu Huang, Jun Liu

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Wenqing DingState Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing 100871, China.
Qidong DengState Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing 100871, China.
Tianyu WangState Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing 100871, China.
Ruoqian LiuYuanpei College, Peking University, Beijing 100871, China.
Yunfan XiangState Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing 100871, China.
Lulu HuangState Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing 100871, China.
Jun LiuState Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing 100871, China.ORCID 0000-0002-2498-9963

Funding

National Key Research and Development Program of China 2023YFC3402200National Key Research and Development Program of China 2024YFA1107000National Natural Science Foundation of China 32170595Natural Science Foundation of Beijing Municipality Z240010Peking UniversityShenzhen Bay Laboratory S241101001
6 · The paper itself

Abstract

External stressors, particularly heat stress, induce DNA damage and genomic instability in cells. However, the mechanisms by which cells rapidly respond to such DNA damage remain largely unknown. In this study, we found that heat shock factor 1 (HSF1), the major transcription factor in the heat shock response, activated several non-homologous end joining (NHEJ) pathway-associated genes, particularly NHEJ1, through puncta formation, thereby maintaining the stability of NHEJ pathway and alleviating the repair burden of DNA double-strand breaks caused by heat stress. Furthermore, N6-methyladenosine (m6A) RNA modification and its reader YTH domain-containing protein 1 (YTHDC1) contributed to this process by promoting the splicing of NHEJ1. Knockdown of HSF1 or YTHDC1 increased nuclear intensity of phosphorylation of histone variant H2AX at Ser-139 (γH2AX) in heat-stressed cells, whereas NHEJ1 overexpression rescued this effect. Moreover, HSF1 or YTHDC1 overexpression increased NHEJ repair efficiency in heat-stressed cells, supporting the existence of an HSF1/YTHDC1-NHEJ1-DNA double-strand repair axis. Our findings reveal a mechanism by which cells repair DNA damage during the heat shock response, providing new insights into how cells maintain genomic stability under external stress conditions.

Indexed as

DNA End-Joining RepairDNA RepairHeat-Shock ResponseHeat Shock Transcription FactorsNerve Tissue ProteinsRNA Splicing FactorsAdenosineDNA Breaks, Double-StrandedDNA DamageGene Expression RegulationHistonesHumansRNA MethylationAdenosineHeat Shock Transcription FactorsHistonesHSF1 protein, humanNerve Tissue ProteinsN-methyladenosineRNA Splicing FactorsYTHDC1 protein, human

Identifiers

PMID42055551
PMCPMC13125758

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.