Sonenberg N
McGill University, Department of Biochemistry, Montreal, Quebec, Canada.
New Biol. 1990 May;2(5):402-9.
Animal viruses have co-evolved with their hosts for millions of years. During this time, the viruses have developed intricate mechanisms to utilize efficiently their host's metabolic pathways, especially those involving macromolecular synthesis, for virus propagation. In particular, many different viruses modulate and usurp their host's translational machinery for use in the synthesis of their own proteins. However, the infected hosts have developed or adapted cellular mechanisms to interdict virus infection. One of these mechanisms is the interferon response, which entails in part a translational regulatory activity that inhibits virus growth. Viruses, in turn, have devised strategies that act as countermeasures to some aspects of the interferon response. These complex virus-host interactions occur at the level of initiation of translation. Two initiation factors, eIF-2 and eIF-4F, play a significant role in a number of virus-host interactions. The recent advances in our understanding of the mode of action of these translation initiation factors have facilitated research on virus-cell interactions at the level of translation. This review is not intended to summarize the general knowledge in this field, but rather to limit the analysis to several examples of virus-host interactions and to speculate on the interplay between the molecular mechanisms involved in these phenomena.
动物病毒与它们的宿主共同进化了数百万年。在此期间,病毒发展出了复杂的机制,以便有效地利用宿主的代谢途径,尤其是那些涉及大分子合成的途径,来进行病毒繁殖。特别地,许多不同的病毒会调节并篡夺宿主的翻译机制,用于合成它们自己的蛋白质。然而,被感染的宿主已经发展出或适应了细胞机制来阻断病毒感染。其中一种机制就是干扰素反应,这部分涉及一种抑制病毒生长的翻译调控活性。反过来,病毒也设计出了一些策略来对抗干扰素反应的某些方面。这些复杂的病毒 - 宿主相互作用发生在翻译起始水平。两种起始因子,即真核生物翻译起始因子2(eIF - 2)和真核生物翻译起始因子4F(eIF - 4F),在许多病毒 - 宿主相互作用中发挥着重要作用。我们对这些翻译起始因子作用方式理解的最新进展促进了在翻译水平上对病毒 - 细胞相互作用的研究。本综述并非旨在总结该领域的一般知识,而是将分析局限于病毒 - 宿主相互作用的几个例子,并推测这些现象所涉及的分子机制之间的相互作用。