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大肠杆菌中转录-翻译耦合的机制

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在大肠杆菌(Escherichia coli,E。coli)等原核生物中,转录和翻译往往是耦合的,这种耦合通常表现在转录和翻译的互相调控上,如转录极性、转录衰减和转录-翻译速率的同步。间接耦合和物理耦合是耦合的两种模式。由警报素(alarmone)(p)ppGpp维持的间接耦合可能需要DksA和TufA蛋白的辅助。物理耦合分为NusG或RfaH因子介导的耦合和非因子条件下产生的"碰撞"耦合。响应于压力的转录或翻译的变化会引发几种耦合模式间的相互转变。耦合对于基因正常表达是必要的,其解除将引发转录终止、R环形成、复制-转录冲突、mRNA切割等不利的事件。结构生物学的相关技术已经清晰地展示了部分耦合的表达体(expressome)的结构细节和特征,这些技术联合多组学分析等方法将提供关于耦合的更深层次的见解。重要的是,对耦合的研究或许会为靶向抗菌药物的开发带来新的思路。
Mechanisms of Transcription-translation Coupling in Escherichia coli
In prokaryotes like Escherichia coli(E.coli),transcription tends to be coupled with translation,which is usually manifested in the mutual regulation of transcription and translation such as transcription polarity,transcription attenuation and synchronization of transcription and translation rates.Indirect coupling and physical coupling are two different models of the coupling.Indirect coupling maintained by the alarmone(p)ppGpp may require the assistance of DksA and TufA proteins.Physical coupling could be divided into those mediated by NusG or RfaH factors and those induced via"collision"under non-factor condition.Changes in transcription or translation in response to pressure will lead to mutual transitions among several coupling modes.Coupling is necessary for normal gene expression,and its release will contribute to adverse events such as transcription termination,R-loop formation,conflict between replication and transcription and mRNA cleavage.The related technologies of structural biology have clearly demonstrated the structural details and characteristics of partial coupled expressomes.These technologies,combined with methods like multiomics analysis,will provide deeper insights into the coupling.Significantly,the study of the coupling may bring new ideas for development of the targeted antibiotics.

Escherichia colitranscription-translation couplingRNA polymeraseribosomeexpressome

沈崇杰、莫日根

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内蒙古大学生命科学学院,省部共建草原家畜生殖调控与繁育国家重点实验室,呼和浩特 010020

大肠杆菌 转录-翻译耦合 RNA聚合酶 核糖体 表达体

国家自然科学基金

32260233

2024

生物化学与生物物理进展
中国科学院生物物理研究所,中国生物物理学会

生物化学与生物物理进展

CSTPCD北大核心
影响因子:0.476
ISSN:1000-3282
年,卷(期):2024.51(3)
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