RNA聚合酶I转录启动的结构基础
Christoph Engel1, Tobias Gubbey1, Simon Neyer1
1Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
Cell
|March 25, 2017
概括
RNA聚合酶I (Pol I) 和启动因子Rrn3和核心因子 (CF) 对于核糖体RNA基因转录至关重要. 结构研究揭示了CF如何与Pol I-Rrn3接,加载DNA,并促进转录启动.
科学领域:
- 分子生物学
- 结构生物学
- 生物化学
背景情况:
- 核糖体RNA (rRNA) 合成对于细胞生长至关重要,需要RNA聚合酶I (Pol I).
- 通过Pol I启动转录涉及启动因子Rrn3和核心因子 (CF).
- 了解Pol I转录启动的结构机制是解读基因调节的关键.
研究的目的:
- 阐明基底RNA聚合酶I转录启动的分子机制.
- 通过Pol I-Rrn3-CF复合体来确定促进体识别和DNA加载的结构基础.
主要方法:
- 射线晶体学
- 冷电子显微镜 (冷电子显微镜)
- 结构建模
主要成果:
- 通过结合X射线结晶学和冷EM获得了基底POLI启动的分子模型.
- 三个子单位的核心因子 (CF) 结合上游促进体DNA并与Pol I-Rrn3复合体对接.
- DNA被载入聚合酶活性中心裂,导致裂收缩和RNA合成的活性构造.
结论:
- 结构模型揭示了Pol I转录启动过程中DNA加载和解的逐步过程.
- 促体特异性是由DNA序列特征 ("可曲性"和"可化性") 决定的,这些特征能够与启动因子和聚合酶相互作用.
- 这项研究提供了关于RNA聚合酶I对rRNA基因转录的调节的基本见解.
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