Masters P S
Wadsworth Center for Laboratories and Research, New York State Department of Health, State University of New York at Albany, New York 12201, USA.
Adv Virus Res. 1999;53:245-64. doi: 10.1016/s0065-3527(08)60351-6.
The capped and polyadenylated genomes of coronaviruses, spanning some 27 to 31 kb, are the largest of all RNA virus genomes, including those of the segmented RNA viruses. This chapter presents the reverse genetics of the largest RNA viruses. Just as all other positive-sense RNA viruses (retroviruses excluded), coronavirus genomic RNA is infectious when transfected into the cells of a permissive host. Therefore, in principle, the most direct way to perform reverse genetics on a coronavirus ought to involve the construction of a full-length genomic complementary DNA (cDNA) clone from which infectious RNA could be transcribed . The method––targeted recombination––is less direct and more laborious, and so far it has been applied exclusively to site-directed mutagenesis of mouse hepatitis virus (MHV). Thus, at least for structural gene mutations that are not expected to be severely deleterious, targeted recombination may remain the less complicated alternative for the creation of MHV mutants. The chapter discusses targeted RNA recombination, such as development of system, genetic analysis of coronavirus structural proteins, genetic analysis of coronavirus RNA synthesis, and limitations of targeted recombination.
冠状病毒的加帽和多聚腺苷酸化基因组约为27至31 kb,是所有RNA病毒基因组中最大的,包括那些分节段RNA病毒的基因组。本章介绍最大RNA病毒的反向遗传学。正如所有其他正链RNA病毒(逆转录病毒除外)一样,冠状病毒基因组RNA转染到允许宿主的细胞中时具有感染性。因此,原则上,对冠状病毒进行反向遗传学的最直接方法应该是构建一个全长基因组互补DNA(cDNA)克隆,从中可以转录出感染性RNA。靶向重组方法不太直接且更费力,到目前为止,它仅应用于小鼠肝炎病毒(MHV)的定点诱变。因此,至少对于预计不会严重有害的结构基因突变,靶向重组可能仍然是创建MHV突变体的较简单替代方法。本章讨论靶向RNA重组,如系统的开发、冠状病毒结构蛋白的遗传分析、冠状病毒RNA合成的遗传分析以及靶向重组的局限性。