Lai M M, Cavanagh D
Department of Molecular Microbiology and Immunology, Howard Hughes Medical Institute, University of Southern California School of Medicine, Los Angeles 90033-1054, USA.
Adv Virus Res. 1997;48:1-100. doi: 10.1016/S0065-3527(08)60286-9.
This chapter discusses the manipulation of clones of coronavirus and of complementary DNAs (cDNAs) of defective-interfering (DI) RNAs to study coronavirus RNA replication, transcription, recombination, processing and transport of proteins, virion assembly, identification of cell receptors for coronaviruses, and processing of the polymerase. The nature of the coronavirus genome is nonsegmented, single-stranded, and positive-sense RNA. Its size ranges from 27 to 32 kb, which is significantly larger when compared with other RNA viruses. The gene encoding the large surface glycoprotein is up to 4.4 kb, encoding an imposing trimeric, highly glycosylated protein. This soars some 20 nm above the virion envelope, giving the virus the appearance-with a little imagination-of a crown or coronet. Coronavirus research has contributed to the understanding of many aspects of molecular biology in general, such as the mechanism of RNA synthesis, translational control, and protein transport and processing. It remains a treasure capable of generating unexpected insights.
本章讨论了冠状病毒克隆以及缺陷干扰(DI)RNA互补DNA(cDNA)的操作,以研究冠状病毒RNA复制、转录、重组、蛋白质加工与运输、病毒粒子组装、冠状病毒细胞受体鉴定以及聚合酶加工。冠状病毒基因组的性质为非节段性、单链、正义RNA。其大小在27至32 kb之间,与其他RNA病毒相比显著更大。编码大表面糖蛋白的基因长达4.4 kb,编码一种巨大的三聚体高度糖基化蛋白。该蛋白在病毒粒子包膜上方约20 nm处突出,使病毒(稍加想象)呈现出皇冠或冕状的外观。冠状病毒研究总体上有助于理解分子生物学的许多方面,如RNA合成机制、翻译控制以及蛋白质运输与加工。它仍然是一个能够产生意外见解的宝库。