过度的DNA双链断裂-相关的3D基因组重组有助于神经管缺陷与叶酸缺乏
Ting Zhang1, Lin Lin2,3, Jianting Li4
1Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, Beijing, 100020, China.
Advanced science (Weinheim, Baden-Wurttemberg, Germany)
|September 18, 2025
概括
怀孕期间叶酸缺乏会增加神经管缺陷 (NTD) 的风险. 这项研究揭示了DNA双链断裂破坏3D基因组组织,影响关闭神经管关闭的关键基因.
科学领域:
- 遗传学 是一个遗传学.
- 发育生物学 发展生物学
- 基因组学就是基因组学.
背景情况:
- 神经管缺陷 (NTD) 是一种常见的先天性形.
- 叶酸缺乏是NTD的已知风险因素,但潜在的机制尚不清楚.
研究的目的:
- 调查DNA双链断裂 (DSB) 在3D基因组组织中的作用,在叶酸缺乏和NTDs的背景下.
主要方法:
- 使用了一个NTD鼠标模型.
- 分析了DNA双链断裂 (DSB) 分布及其与3D基因组组织的相关性.
- 检查了RNA聚合酶II (Pol II) 的停滞和R循环形成.
- 评估了神经管关闭相关基因中的染色体循环结构和基因表达.
主要成果:
- NTD小鼠模型表现出大量的DSB,破坏了3D基因组组织.
- 活跃基因中的DSB会阻断Pol II并形成R循环.
- DSB频率与转录开始地点的基因距离负相关.
- 增强剂中增加的DSBs会取代染色质循环,影响神经管闭合基因.
结论:
- 过度的DSBs在叶酸缺乏的NTD中破坏了3D基因组组织.
- 这种干扰导致神经管关闭所必需的基因失调.
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