Excessive DNA Double‐Strand Breaks–Associated 3D Genome Reorganization Contributes to Neural Tube Defects with Folate Deficiency

Neural tube defects (NTDs) are one of the most common congenital malformations. Folic acid deficiency in pregnant women increases the risk of developing NTDs; however, the underlying etiology and mechanisms remain elusive. In this study, the role of DNA double-strand breaks (DSBs) in 3D genome organization in NTDs with folate deficiency is reported. The NTD mouse model is burdened with abundant DSBs associated with the disruption of 3D genome organization. DSBs occurring in active genes lead to the stalling of RNA polymerase II (Pol II) and formation of R-loops in the 3D genome. The DSB ratios of the genomic regions negatively correlated with the distance from the transcription start sites of the gene. The DSB ratios of the proximal and distal enhancers are significantly higher and induce the displacement of loops with busy anchors. Furthermore, DSB-associated dysregulation of chromatin loops occurs in neural tube closure-associated genes that are abnormally expressed in human NTDs. Taken together, excessive DSB-associated 3D genome organization disruption within NTDs with folate deficiency contributes to the dysregulation of neural tube closure-associated genes.

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Publication Details

Journal
Advanced Science
Published
2025-09-18
DOI
https://doi.org/10.1002/advs.202410603
Primary Topic
Prenatal Screening and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00

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article

Excessive DNA Double‐Strand Breaks–Associated 3D Genome Reorganization Contributes to Neural Tube Defects with Folate Deficiency

Caihua Li, Hebing Chen, Shengjun Liang, Xuemei Bai et al.
Advanced Science
Prenatal Screening and Diagnostics
article

Excessive DNA Double‐Strand Breaks–Associated 3D Genome Reorganization Contributes to Neural Tube Defects with Folate Deficiency

Caihua Li, Hebing Chen, Shengjun Liang, Xuemei Bai, Jianting Li, Fang Wang, Lin Lin, Hao Li, Dan Guo, Ting Zhang, Qiu Xie, Xiaochen Bo, Yihua Bao
article en

Abstract

Neural tube defects (NTDs) are one of the most common congenital malformations. Folic acid deficiency in pregnant women increases the risk of developing NTDs; however, the underlying etiology and mechanisms remain elusive. In this study, the role of DNA double-strand breaks (DSBs) in 3D genome organization in NTDs with folate deficiency is reported. The NTD mouse model is burdened with abundant DSBs associated with the disruption of 3D genome organization. DSBs occurring in active genes lead to the stalling of RNA polymerase II (Pol II) and formation of R-loops in the 3D genome. The DSB ratios of the genomic regions negatively correlated with the distance from the transcription start sites of the gene. The DSB ratios of the proximal and distal enhancers are significantly higher and induce the displacement of loops with busy anchors. Furthermore, DSB-associated dysregulation of chromatin loops occurs in neural tube closure-associated genes that are abnormally expressed in human NTDs. Taken together, excessive DSB-associated 3D genome organization disruption within NTDs with folate deficiency contributes to the dysregulation of neural tube closure-associated genes.

Advanced ScienceVol. 12(47)
Harbin Medical University (CN), Shanxi University (CN), Northeast Normal University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Beijing Normal University (CN), Peking Union Medical College Hospital (CN), Institute for Transfusion Medicine (US), Shanghai Genon Biological Products (China) (CN), Shanghai CASB Biotechnology (China) (CN), Capital Institute of Pediatrics (CN), Institute of Coal Chemistry (CN)
National Health Commission of the People's Republic of China, National Key Research and Development Program of China
Openalex Percentile: Top 65%
Prenatal Screening and Diagnostics
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