概括
细菌RNA在转录启动过程中获得尼古丁胺腺素二核酸 (NAD+) 或3′- 脱酸- 共酶A (dpCoA),而不是之后. 这种非正规启动核酸 (NCIN) 限制机制在体内发生,并影响RNA功能.
科学领域:
- 分子生物学
- 生物化学
- 遗传学
背景情况:
- RNA的5′端显著影响其稳定性,处理,局部化和翻译.
- 转录组调节包括在真核RNA中发现的5′帽子等修饰.
- 已观察到细菌RNA具有类似于真核细胞的5′端,例如尼古丁胺腺素二核酸 (NAD+) 或3′-脱酶A (dpCoA).
研究的目的:
- 阐明NAD+,NADH和dpCoA在细菌RNA中的结合机制.
- 要确定这些封顶是在转录后或转录启动期间添加的.
- 调查这种限制过程的结构基础和功能后果.
主要方法:
- 使用来自细菌和真核生物的RNA聚合酶 (RNAP II).
- 分析了促进体DNA序列在调节限制效率中的作用.
- 确定非正规启动核酸 (NCIN) 限制的体内发生和功能影响.
- 获得的转录启动复合物的晶体结构与NCIN覆盖的RNA.
主要成果:
- 证明NAD+,NADH和dpCoA在RNAP的新转录启动过程中被纳入非正规启动核酸 (NCIN).
- 表明细菌和真核RNAP II可以结合NCIN盖.
- 鉴定出促体DNA序列是NCIN限制效率的关键决定因素.
- 证实NCIN上限发生在体内并且具有功能性后果.
- 提供了晶体结构,揭示了NCIN封顶的机制和结构基础.
结论:
- 在转录启动过程中发生的ab initio过程,而不是转录后的修改.
- 这种机制涉及NAD+,NADH和dpCoA,在细菌和真核RNAP II中保存.
- 激发器序列决定了NCIN上限的效率.
- 以NCIN为媒介的初始上限可能是生活各个领域广泛的监管机制.
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