共转录RNA封闭酶在暂停转录复合体上的结构
Yan Li1, Qianmin Wang1, Yanhui Xu1,2
1Fudan University Shanghai Cancer Center, Institutes of Biomedical Sciences, State Key Laboratory of Genetic Engineering and Shanghai Key Laboratory of Medical Epigenetics, Shanghai Medical College of Fudan University, Shanghai, 200032, China.
这项研究揭示了RNA guanylyltransferase (RNGTT) 和2'-O-ribose甲基转移酶 (CMTR1) 在转录暂停期间如何与RNA聚合酶II结合. 这种结合对于前mRNA的5'-end capping至关重要,这是RNA处理的关键步骤.
科学领域:
- 分子生物学分子生物学
- 结构生物学 结构生物学
- 生物化学 生物化学
背景情况:
- 5'-end capping是RNA处理的初始步骤,涉及瓜诺辛添加和2'-O- рибо甲基化.
- 这些限制事件与RNA聚合酶II的早期转录同时发生,特别是在暂停期间.
研究的目的:
- 确定与RNGTT和CMTR1.1结合的暂停延长复合体的冷电子显微镜 (cryo-EM) 结构.
- 为了阐明5'-end capping在转录暂停期间的机制.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于解析暂停延长复合物的结构.
- 分析涉及RNA聚合酶II,RNGTT,CMTR1和NELF复合物的复合物.
主要成果:
- 结构显示RNGTT和NELF复合体与RNA聚合酶II同时结合.
- NELF复合体显示了两个构造,其中一个显示了NELF-A/D重新排列.
- CMTR1位于RNA聚合酶II茎上与RNGTT相邻,表明直接结合.
结论:
- RNGTT和CMTR1直接与暂停延长复合体结合.
- 确定的结构揭示了5'-end前mRNA在转录暂停期间封闭的机制.
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