Cordes Susann, Kusov Yuri, Heise Tilman, Gauss-Müller Verena
Institute of Medical Molecular Biology, University of Lübeck, Ratzeburger Allee 160, D-23538 Lübeck, Germany.
Biochem Biophys Res Commun. 2008 Apr 18;368(4):1014-9. doi: 10.1016/j.bbrc.2008.01.163. Epub 2008 Feb 20.
The human RNA-binding protein La, is an essential trans-acting factor in IRES-dependent translation initiation of poliovirus, the prototypic picornavirus. For hepatitis A virus (HAV), an unusual member of this virus family, the role of host proteins in its inefficient translation and slow replication is unclear. Using small interfering RNA in vivo and purified La in vitro, we demonstrate for the first time that La suppresses HAV IRES-mediated translation and replication. We show that La binds specifically to distinct parts of the HAV IRES and that-unlike poliovirus-HAV proteinase 3C does not cleave La. The La-mediated suppression of HAV translation and stimulation of poliovirus translation implies unexpected mechanistic differences between viral IRES elements.
人类RNA结合蛋白La是脊髓灰质炎病毒(典型的微小核糖核酸病毒)内部核糖体进入位点(IRES)依赖性翻译起始过程中必不可少的反式作用因子。对于甲型肝炎病毒(HAV),这个病毒家族的一个特殊成员,宿主蛋白在其低效翻译和缓慢复制中的作用尚不清楚。我们通过体内使用小干扰RNA和体外使用纯化的La,首次证明La抑制HAV IRES介导的翻译和复制。我们表明La特异性结合HAV IRES的不同部分,并且与脊髓灰质炎病毒不同,HAV蛋白酶3C不会切割La。La介导的对HAV翻译的抑制和对脊髓灰质炎病毒翻译的刺激意味着病毒IRES元件之间存在意想不到的机制差异。