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通过跨物种S-化对微RNA机制的调节和发展
Puneet Seth1, Paishiun N Hsieh2, Suhib Jamal1
1Institute for Transformative Molecular Medicine and Department of Medicine, Case Western Reserve University School of Medicine and University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA.
Cell
|February 23, 2019
概括
肠道微生物群产生氧化,改变宿主蛋白和微RNA功能. 这种细菌信号影响了C. elegans的基因表达和发育,揭示了新的沟通途径.
科学领域:
- 微生物学
- 分子生物学
- 发育生物学
背景情况:
- 主体微生物群的相互作用对细胞功能至关重要.
- 微生物与宿主之间的物种间交流机制在很大程度上是未知的.
- 氧化 (NO) 是一种具有多种生物作用的气体传递物.
研究的目的:
- 研究微生物分子如何影响宿主细胞功能.
- 阐明来自居住细菌的氧化在宿主蛋白质组修饰中的作用.
- 了解微生物群依赖蛋白质S-化对宿主基因表达和发育的影响.
主要方法:
- 使用模型生物C.
- 研究居住细菌的氧化产量.
- 分析了宿主蛋白质的S-化,包括阿尔戈诺特 (ALG-1).
- 操纵氧化生成和S-化路径.
主要成果:
- 微生物来源的氧化诱导了C. elegans宿主蛋白质的广泛S-化.
- 在哺乳动物AGO2中保存的ALG-1的微生物依赖性S-化改变了其微RNA介导的基因调节功能.
- 消除氧化生成或ALG- 1 S- 化对宿主发育产生了显著的影响.
结论:
- 肠道微生物群可以塑造宿主的转化后的环境.
- 微生物信号调节微RNA活动,基因表达和宿主发育.
- 这项研究揭示了一种新的宿主微生物群沟通机制,涉及气传递物和蛋白质S-化.
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