在IRES-依赖的翻译中,Enterovirus A71对酸化的SR蛋白的颠覆被RNA-相互作用组分析揭示出来
Kuo-Ming Lee1,2,3, Chih-Ching Wu2,4,5,6, Yu-Ting Fan1
1International Master Degree Program for Molecular Medicine in Emerging Viral Infections, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
PLoS pathogens
|June 16, 2025
概括
病毒感染涉及复杂的RNA管理. 这项研究表明,对于肠道病毒A71 (EV-A71) 复制至关重要的富含氨酸和氨酸 (SR) 的蛋白质被酸化并移动到细胞质中,在早期感染期间帮助病毒翻译.
科学领域:
- 病毒学 病毒学
- 分子生物学分子生物学
- 在RNA生物学,RNA生物学.
背景情况:
- 在感染期间了解病毒RNA命运至关重要.
- 肠道病毒A71 (EV-A71) 感染动态涉及复杂的RNA-蛋白相互作用.
- 核糖核蛋白复合体 (RNP) 协调病毒RNA的处理.
研究的目的:
- 在EV-A71感染期间调查时间RNP组成.
- 阐明富含胺和氨酸 (SR) 蛋白在EV-A71复制中的作用.
- 探索SR蛋白调作为一种抗病毒标.
主要方法:
- 使用代谢标记和定量蛋白质组学进行RNA-相互作用组分析.
- 在早期 (日食) 和晚期 (成熟) 感染阶段对RNP进行比较分析.
- 破坏SR蛋白并抑制SR蛋白酸化.
主要成果:
- EV-A71感染诱导了通过SR蛋白酸化和细胞质再定位的动态RNP重塑.
- 抑制SRSF4,SRSF5和SRSF6可显著降低病毒生长.
- 在早期感染期间,化SR蛋白与翻译机制共分.
- 抑制SR蛋白酸化会影响依赖IRES的翻译和病毒复制.
结论:
- 在EV-A71感染的日食阶段,SR蛋白调节对于促进翻译能力复合体至关重要.
- 向SR蛋白酸化是针对EV-A71的有希望的抗病毒策略.
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