核素诱导在释放mRNA核出口块中的作用
Jost Enninga1, David E Levy, Günter Blobel
1Laboratory of Cell Biology, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021, USA.
概括
干扰素 (IFN) 调节核素Nup98和Nup96,逆转膀性口腔炎病毒矩阵蛋白抑制mRNA出口. 这种IFN介导的机制恢复了基因表达.
科学领域:
- 细胞生物学 细胞生物学
- 病毒学 病毒学
- 分子生物学分子生物学
背景情况:
- 核孔综合体 (NPC) 调节核细胞质运输.
- 核波林 (Nups) Nup98和Nup96是核内部发现的NPC组成部分.
- 膀性口炎病毒 (VSV) 矩阵 (M) 蛋白通过准Nup98.8来抑制信使RNA (mRNA) 核出口.
研究的目的:
- 调查干扰素 (IFN) 对Nup98和Nup96表达的影响.
- 确定IFN是否可以逆转M蛋白介导的mRNA出口抑制.
主要方法:
- 用IFN-gamma进行细胞治疗.
- 通过编码Nup98和Nup96.的互补DNA (cDNA) 进行转染.
- 对mRNA核出口和基因表达的分析.
主要成果:
- 干扰素 (IFN) 对Nup98和Nup96.6的表达进行上调.
- IFN-玛治疗或Nup98/Nup96cDNA转染逆转了M蛋白诱导的mRNA出口的抑制.
- 增加Nup98和Nup96的表达抵消了M蛋白对基因表达的抑制作用.
结论:
- 对Nup98和Nup96的IFN上调是一种天生的免疫机制.
- 这种机制有效地逆转了病毒对宿主基因表达的抑制.
- Nup98和Nup96通过恢复mRNA输出,在抗病毒防御中发挥关键作用.
相关概念视频
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