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冠状病毒复制结构的发生和动态。

Biogenesis and dynamics of the coronavirus replicative structures.

机构信息

Virology Division, Department of Infectious Diseases & Immunology, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, 3584 CL Utrecht, The Netherlands.

出版信息

Viruses. 2012 Nov 21;4(11):3245-69. doi: 10.3390/v4113245.

Abstract

Coronaviruses are positive-strand RNA viruses that are important infectious agents of both animals and humans. A common feature among positive-strand RNA viruses is their assembly of replication-transcription complexes in association with cytoplasmic membranes. Upon infection, coronaviruses extensively rearrange cellular membranes into organelle-like replicative structures that consist of double-membrane vesicles and convoluted membranes to which the nonstructural proteins involved in RNA synthesis localize. Double-stranded RNA, presumably functioning as replicative intermediate during viral RNA synthesis, has been detected at the double-membrane vesicle interior. Recent studies have provided new insights into the assembly and functioning of the coronavirus replicative structures. This review will summarize the current knowledge on the biogenesis of the replicative structures, the membrane anchoring of the replication-transcription complexes, and the location of viral RNA synthesis, with particular focus on the dynamics of the coronavirus replicative structures and individual replication-associated proteins.

摘要

冠状病毒是正链 RNA 病毒,是动物和人类重要的传染性病原体。正链 RNA 病毒的一个共同特征是它们在细胞质膜上组装复制转录复合物。感染后,冠状病毒会广泛地将细胞膜重组成具有双层膜囊泡和卷曲膜的类细胞器复制结构,涉及 RNA 合成的非结构蛋白定位于这些结构上。双链 RNA 可能在病毒 RNA 合成过程中作为复制中间体发挥作用,已在双层膜囊泡内部检测到。最近的研究为冠状病毒复制结构的组装和功能提供了新的见解。本综述将总结复制结构生物发生、复制转录复合物的膜锚定以及病毒 RNA 合成位置的最新知识,特别关注冠状病毒复制结构和单个复制相关蛋白的动态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1742/3509692/aefc6bd2f4ed/viruses-04-03245-g001.jpg

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