DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genome
Abstract Background G-quadruplex structures (G4s) have been identified in the genomes of many organisms and have been proven to play significant epigenetic regulatory roles in gene transcription. Intriguingly, only a small portion of the predicted G4-forming sequences can fold into G4s under cellula...
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BMC
2025-07-01
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| Series: | Genome Biology |
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| Online Access: | https://doi.org/10.1186/s13059-025-03678-4 |
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| author | Kangkang Niu Lijun Xiang Xiaojuan Zhang Xiaoyu Li Tingting Yao Jin Li Chu Zhang Junpeng Liu Yuling Peng Guanfeng Xu Hui Xiang Hao Wang Qisheng Song Qili Feng |
| author_facet | Kangkang Niu Lijun Xiang Xiaojuan Zhang Xiaoyu Li Tingting Yao Jin Li Chu Zhang Junpeng Liu Yuling Peng Guanfeng Xu Hui Xiang Hao Wang Qisheng Song Qili Feng |
| author_sort | Kangkang Niu |
| collection | DOAJ |
| description | Abstract Background G-quadruplex structures (G4s) have been identified in the genomes of many organisms and have been proven to play significant epigenetic regulatory roles in gene transcription. Intriguingly, only a small portion of the predicted G4-forming sequences can fold into G4s under cellular conditions. Here, we employ publicly available data, methylation inhibitors, DNA methyltransferase 1 (DNMT1) knockout, and multiple ‘Omics’ technologies to study the interplay between DNA methylation and chromatin accessibility on G4 formation and the impact on gene expression. Results We find an antagonistic correlation between genomic 5mC DNA methylation level and G4 abundance. The abundance of genomic G4s significantly increases when the genome-wide methylation level is reduced by methylation inhibitor treatment or DNMT1 knockout. The increase in G4 signals in DNMT1 knockout cells is reversed by DNMT1 overexpression. Combined ATAC-seq, whole genome bisulfite sequencing, and G4 CUT&Tag analyses demonstrate that 5mC DNA methylation inhibits G4 formation in both open and closed chromatin states. The inhibitory effect of 5mC modification on the formation of G4s is verified by circular dichroism and electrophoretic mobility shift assay in vitro. G4 CUT&Tag and RNA-seq analyses reveal that reduced DNA methylation enhances G4 formation and promotes the transcription of nearby genes. Conclusions This study demonstrates that 5mC DNA methylation directly inhibits G4 formation in the genome and modulates subsequent gene transcription, confirming the interaction between G4s and DNA methylation as an important mechanism for epigenetic regulation of gene transcription. |
| format | Article |
| id | doaj-art-740544e2bb5f49c69c845a656600da11 |
| institution | Kabale University |
| issn | 1474-760X |
| language | English |
| publishDate | 2025-07-01 |
| publisher | BMC |
| record_format | Article |
| series | Genome Biology |
| spelling | doaj-art-740544e2bb5f49c69c845a656600da112025-08-20T04:03:02ZengBMCGenome Biology1474-760X2025-07-0126112310.1186/s13059-025-03678-4DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genomeKangkang Niu0Lijun Xiang1Xiaojuan Zhang2Xiaoyu Li3Tingting Yao4Jin Li5Chu Zhang6Junpeng Liu7Yuling Peng8Guanfeng Xu9Hui Xiang10Hao Wang11Qisheng Song12Qili Feng13Guangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversitySouth China Normal University-Panyu Central Hospital Joint Laboratory of Basic and Translational Medical Research, Guangzhou Panyu Central HospitalDivision of Plant Sciences and Technology, University of MissouriGuangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal UniversityAbstract Background G-quadruplex structures (G4s) have been identified in the genomes of many organisms and have been proven to play significant epigenetic regulatory roles in gene transcription. Intriguingly, only a small portion of the predicted G4-forming sequences can fold into G4s under cellular conditions. Here, we employ publicly available data, methylation inhibitors, DNA methyltransferase 1 (DNMT1) knockout, and multiple ‘Omics’ technologies to study the interplay between DNA methylation and chromatin accessibility on G4 formation and the impact on gene expression. Results We find an antagonistic correlation between genomic 5mC DNA methylation level and G4 abundance. The abundance of genomic G4s significantly increases when the genome-wide methylation level is reduced by methylation inhibitor treatment or DNMT1 knockout. The increase in G4 signals in DNMT1 knockout cells is reversed by DNMT1 overexpression. Combined ATAC-seq, whole genome bisulfite sequencing, and G4 CUT&Tag analyses demonstrate that 5mC DNA methylation inhibits G4 formation in both open and closed chromatin states. The inhibitory effect of 5mC modification on the formation of G4s is verified by circular dichroism and electrophoretic mobility shift assay in vitro. G4 CUT&Tag and RNA-seq analyses reveal that reduced DNA methylation enhances G4 formation and promotes the transcription of nearby genes. Conclusions This study demonstrates that 5mC DNA methylation directly inhibits G4 formation in the genome and modulates subsequent gene transcription, confirming the interaction between G4s and DNA methylation as an important mechanism for epigenetic regulation of gene transcription.https://doi.org/10.1186/s13059-025-03678-4DNA methylationG-quadruplex formationEpigenetic regulationGene expression |
| spellingShingle | Kangkang Niu Lijun Xiang Xiaojuan Zhang Xiaoyu Li Tingting Yao Jin Li Chu Zhang Junpeng Liu Yuling Peng Guanfeng Xu Hui Xiang Hao Wang Qisheng Song Qili Feng DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genome Genome Biology DNA methylation G-quadruplex formation Epigenetic regulation Gene expression |
| title | DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genome |
| title_full | DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genome |
| title_fullStr | DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genome |
| title_full_unstemmed | DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genome |
| title_short | DNA 5mC methylation inhibits the formation of G-quadruplex structures in the genome |
| title_sort | dna 5mc methylation inhibits the formation of g quadruplex structures in the genome |
| topic | DNA methylation G-quadruplex formation Epigenetic regulation Gene expression |
| url | https://doi.org/10.1186/s13059-025-03678-4 |
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