人类核外体体适配器NEXT和PAXT与转录终止和处理机械的直接合
Christopher C Kuhn1, Mahesh K Chand1, Sofia Todesca1
1Department of Structural Cell Biology, Max Planck Institute of Biochemistry, Martinsried 82152, Germany.
这项研究揭示了核EXosome向 (NEXT) 和Poly(A) 尾部EXosome向 (PAXT) 适配器如何将RNA聚合酶II (Pol II) 转录终结与核RNA质量控制联系起来. 这涉及与整合器和裂变和多化复合物的新型相互作用.
科学领域:
- 分子生物学分子生物学
- 结构生物学 结构生物学
- 在RNA生物学,RNA生物学.
背景情况:
- 核外体向适配器 (NEXT和PAXT) 降解异常的RNA聚合酶II (Pol II) 转录.
- 这些适配器与转录终止机器之间的相互作用尚不清楚.
研究的目的:
- 阐明连接转录终结复合体与核RNA质量控制途径的分子机制.
- 为了建模NEXT/PAXT适配器与集成器/裂变和多化 (CPA) 复合体之间的以前未报告的相互作用.
主要方法:
- 在蛋白质复合体的状结构预测.
- 在体外生化测试.
- 单粒子冷电子显微镜 (冷电子显微镜).
主要成果:
- 鉴定出ZC3H18蛋白是整合器和CPA复合体之间的桥梁.
- ZC3H18直接绑定了集成器 (INTS9/11) 和CPA (mPSF) 组件.
- 通过相互排斥的结合,ZC3H18与NEXT和PAXT适配器相互作用.
- 观察到PAXT组件与CPA的替代配置.
结论:
- 一个多功能交互网络将转录终止与核RNA质量控制联系起来.
- 这些发现揭示了涉及ZC3H18,整合器,CPA,NEXT和PAXT的新型结构框架.
- 这项研究促进了对RNA处理和核中的质量控制的理解.
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