脊髓灰质炎病毒转录的结构基础:转录和封装疫苗复合物
Hauke S Hillen1, Julia Bartuli2, Clemens Grimm2
1Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
Cell
|December 14, 2019
概括
脊髓灰质炎病毒通过病毒RNA聚合酶 (vRNAPs) 和封闭酶合成传递 RNA (mRNAs). 这项研究揭示了这些复合物的冷电子显微镜结构,解释了mRNA的合成和修饰.
科学领域:
- 病毒学
- 结构生物学
- 分子生物学
背景情况:
- 脊髓灰质炎病毒依赖病毒编码的RNA聚合酶 (vRNAPs) 和RNA处理因子在宿主细胞质中进行mRNA合成和封闭.
- 之前的研究报告了核心和完整的 Vaccinia poxvirus vRNAP 复合物的结构.
研究的目的:
- 通过冷电子显微镜 (cryo-EM) 呈现 Vaccinia vRNAP 在转录延长和同转录封闭复合体中的结构.
- 阐明天花病毒RNA合成和共转录修饰的结构基础.
主要方法:
- 使用冷电子显微镜 (cryo-EM) 来确定 Vaccinia vRNAP 复合物的结构.
- 进行结构比较以分析转录和封闭过程中的重排.
主要成果:
- 获得了 Vaccinia vRNAP 的延长和共转录封闭复合物的结构.
- 病毒封闭酶 (CE) 形成两个移动模块,与RNA退出道周围的聚合酶相互作用.
- 从vRNAP活性部位到CE三酸酶活性部位的RNA进展被可视化.
- 在从启动到封闭和延长的过渡过程中,观察到转录机制的大规模重组.
结论:
- 这些结构揭示了天花病毒如何合成和共同转录地修改它们的RNA.
- 了解这些机制可以了解天花病毒基因表达的分子机制.
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