RNA结构可塑性在调节HIV-1基因组包装和翻译中的作用
Saif Yasin1, Sydney L Lesko2,3, Siarhei Kharytonchyk4
1Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, MD 21250.
概括
艾滋病毒-1RNA包装是由瓜诺辛启动控制的. 配有三个关诺辛 (3G) 的RNAs形成了将5'盖封闭的结构,防止包装并有利于翻译.
科学领域:
- 分子生物学分子生物学
- 病毒学 病毒学
- 生物物理学的生物物理.
背景情况:
- 艾滋病毒-1 (人类免疫缺陷病毒1型) 的RNA包装成后代病毒是一个复杂的过程.
- 双胞胎转录起点的使用,产生单一 (1G) 或三重 (3G) 瓜诺辛启动的RNA,影响RNA命运.
- 5'聚A元素在RNA结构和功能中起作用.
研究的目的:
- 研究HIV-1转录中的5'聚A元素的结构重塑如何影响RNA包装和翻译.
- 确定5'盖暴露在病毒基因组包装中的作用.
主要方法:
- 在体外生物物理研究.
- 细胞内基因组包装试验. 细胞内基因组包装试验.
- 竞争性的翻译分析.
- 对原生和5' polyA突变体转录的分析.
主要成果:
- 在3GRNA中稳定5'多A发针的突变促进了RNA二分化和Gag结合,而无需帽子绑定.
- 稳定发针结构的3G成绩单没有得到竞争性的包装.
- 对于所有检查的RNAs来说,5' cap暴露与糟糕的包装和高效的翻译相关.
结论:
- 5'盖暴露是HIV-1基因组包装的关键决定因素.
- 5'领导区域的结构可塑性调节HIV-1转录的结构和功能.
- 热力学控制RNA结构影响病毒RNA命运.
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