Wessels Els, Duijsings Daniël, Niu Ting-Kuang, Neumann Steffi, Oorschot Viola M, de Lange Frank, Lanke Kjerstin H W, Klumperman Judith, Henke Andreas, Jackson Catherine L, Melchers Willem J G, van Kuppeveld Frank J M
Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen Centre for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands.
Dev Cell. 2006 Aug;11(2):191-201. doi: 10.1016/j.devcel.2006.06.005.
Many viruses modify cellular processes for their own benefit. The enterovirus 3A protein inhibits endoplasmic reticulum (ER)-to-Golgi transport, a function previously suggested to be important for viral suppression of immune responses. Here, we show that a virus carrying a 3A protein defective in inhibiting ER-to-Golgi transport is indeed less virulent in mice, and we unravel the mechanism by which 3A inhibits this trafficking step. Evidence is provided that 3A inhibits the activation of the GTPase ADP-ribosylation factor 1 (Arf1), which regulates the recruitment of the COP-I coat complex to membranes. 3A specifically inhibits the function of GBF1, a guanine nucleotide exchange factor for Arf1, by interacting with its N terminus. By specifically interfering with GBF1-mediated Arf1 activation, 3A may prove a valuable tool in dissecting the early steps of the secretory pathway.
许多病毒会为自身利益而改变细胞进程。肠道病毒3A蛋白会抑制内质网(ER)到高尔基体的转运,此前有研究表明这一功能对于病毒抑制免疫反应很重要。在此,我们发现携带一种在抑制ER到高尔基体转运方面存在缺陷的3A蛋白的病毒在小鼠体内的毒性确实较低,并且我们揭示了3A抑制这一转运步骤的机制。有证据表明,3A会抑制GTP酶ADP核糖基化因子1(Arf1)的激活,而Arf1可调节COP-I衣被复合体向膜的募集。3A通过与鸟嘌呤核苷酸交换因子GBF1的N端相互作用,特异性地抑制GBF1的功能,而GBF1是Arf1的鸟嘌呤核苷酸交换因子。通过特异性干扰GBF1介导的Arf1激活,3A可能会成为剖析分泌途径早期步骤的一个有价值的工具。