Biogenesis and Dynamics of the Coronavirus Replicative Structures

被引:61
作者
Hagemeijer, Marne C. [1 ]
Rottier, Peter J. M. [1 ]
de Haan, Cornelis A. M. [1 ]
机构
[1] Univ Utrecht, Div Virol, Dept Infect Dis & Immunol, Fac Vet Med, NL-3584 CL Utrecht, Netherlands
来源
VIRUSES-BASEL | 2012年 / 4卷 / 11期
关键词
coronavirus; replication complex; nonstructural protein; membrane rearrangements; protein-protein interactions; live cell imaging; dynamics; RNA synthesis; RESPIRATORY SYNDROME CORONAVIRUS; MOUSE HEPATITIS-VIRUS; OPEN READING FRAME; PROTEIN-PROTEIN INTERACTIONS; HOST GENE-EXPRESSION; SARS-CORONAVIRUS; ENDOPLASMIC-RETICULUM; RNA REPLICATION; VIRAL REPLICATION; DENGUE VIRUS;
D O I
10.3390/v4113245
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:3245 / 3269
页数:25
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