RNA聚合酶II在活性促进体上协调基因组脱乙基化
Jackson A Hoffman1, Kevin W Trotter1, Trevor K Archer1
1Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, Durham, 27709 NC, USA.
在基因促进体中,活性基因素的修饰独立于转录发生. 抑制转录启动实际上增加了基因素乙化和H2AZ,这表明转录消除了这些标记以控制基因活性.
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.
- 基因规则 基因规则
背景情况:
- 具有特定基因素修饰和变异的核体标志着活跃的基因促进体.
- 这些标记被认为可以创建一个开放的染色质结构,有利于转录.
- 有矛盾的证据表明,这些组织蛋白修饰对活跃转录的依赖性.
研究的目的:
- 为了研究活跃的基因组修饰和转录启动之间的关系.
- 为了确定活跃的质子修饰是否需要持续的转录.
主要方法:
- 使用triptolide抑制转录启动以降解RNA聚合酶II.
- 对转录起始点 (TSS) 和增强剂中的基因组修饰的分析.
- 评估p300活性和素脱乙酶抑制.
主要成果:
- 在TSS和增强剂的活性组素修饰独立于转录启动.
- 阻断转录启动导致激素乙化增加和H2AZ在活跃的TSS中被纳入.
- 这种增加是独立于p300活性,但被基因素脱乙酶抑制所掩盖.
结论:
- 活跃的组织蛋白修饰是独立于转录的.
- 转录可能在消除这些修改以调节基因表达方面发挥作用.
- 这表明一个反机制,转录通过修改删除限制了自己的启动.
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