Vande Woude G F, Polatnick J, Ascione R
J Virol. 1970 Apr;5(4):458-63. doi: 10.1128/JVI.5.4.458-463.1970.
The kinetics of ribonucleic acid (RNA) and protein synthesis and RNA methylation were examined after foot-and-mouth disease virus (FMDV) infection of baby hamster kidney cells. The synthesis of RNA extracted from the whole cells was stimulated two- to threefold above the control level of synthesis. This increased rate was attributed to viral RNA synthesis. The inhibition of host RNA methylation was concomitant with but more pronounced than protein synthesis inhibition. The methylation of transfer RNA was initially inhibited by virus infection, but rose to within 70 to 80% of the control level just prior to the production of maximal amounts of virus-specific RNA polymerase. Cycloheximide studies showed that rapid cessation of protein synthesis did not result in the immediate cessation of RNA methylation. A comparison between the kinetics of inhibition of these processes by cycloheximide and FMDV infection suggests that FMDV selectively inhibits RNA methylation.
在口蹄疫病毒(FMDV)感染幼仓鼠肾细胞后,对核糖核酸(RNA)、蛋白质合成及RNA甲基化的动力学进行了研究。从全细胞中提取的RNA合成量比对照合成水平提高了两到三倍。这种增加的速率归因于病毒RNA的合成。宿主RNA甲基化的抑制与蛋白质合成抑制同时发生,但比蛋白质合成抑制更为明显。病毒感染最初会抑制转运RNA的甲基化,但在产生最大量的病毒特异性RNA聚合酶之前,其甲基化水平会升至对照水平的70%至80%。环己酰亚胺研究表明,蛋白质合成的快速停止并不会导致RNA甲基化立即停止。通过环己酰亚胺和FMDV感染对这些过程抑制动力学的比较表明,FMDV选择性地抑制RNA甲基化。