基因组乙化对转录因子进入核细胞DNA的积极作用
1Laboratory of Molecular Embryology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Cell
|January 15, 1993
概括
基因组尾的乙化有助于转录因子TFIIIA与染色质中的DNA结合. 这种修改释放了由基因素尾部施加的限制,改善了基因调节的可访问性.
科学领域:
- 分子生物学分子生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 染色体结构 染色体结构
背景情况:
- 核心组织基因组将DNA包装成核体,形成染色体.
- 基因素N端尾对染色质结构和调节至关重要.
- 转录因子与DNA结合通常受到色素的限制.
研究的目的:
- 为了研究质子N端尾化在TFIIIA与5SRNA基因结合中的作用.
- 确定 histone 乙化如何影响转录因子对染色质中的 DNA 的可访问性.
主要方法:
- 使用模型染色素模板.
- 研究了N-终端尾部乙化和去除对TFIIIA识别的影响.
- 评估结合独立于基因组-DNA相互作用和DNA螺旋重复变化.
主要成果:
- 基因素N端尾的乙化直接促进TFIIIA对5SRNA基因的识别.
- 这种促进独立于基因组-DNA相互作用或DNA螺旋重复的变化.
- 删除基因组尾部还可以增强TFIIIA与核细胞样本的关联.
结论:
- 基斯顿尾巴限制了转录因子进入DNA的机会.
- 基因组尾巴的乙化通过促进尾巴解离或改变DNA配置来释放这种限制.
- 希斯乙化显著影响调节分子对染色质的可访问性.
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