McBride Corrin E, Li Jie, Machamer Carolyn E
Department of Cell Biology, The Johns Hopkins University School of Medicine, 725 N. Wolfe Street, Baltimore, MD 21205, USA.
J Virol. 2007 Mar;81(5):2418-28. doi: 10.1128/JVI.02146-06. Epub 2006 Dec 13.
Like other coronaviruses, severe acute respiratory syndrome coronavirus (SARS CoV) assembles at and buds into the lumen of the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC). Accumulation of the viral envelope proteins at this compartment is a prerequisite for virus assembly. Previously, we reported the identification of a dibasic motif (KxHxx) in the cytoplasmic tail of the SARS CoV spike (S) protein that was similar to a canonical dilysine ER retrieval signal. Here we demonstrate that this motif is a novel and functional ER retrieval signal which reduced the rate of traffic of the full-length S protein through the Golgi complex. The KxHxx motif also partially retained two different reporter proteins in the ERGIC region and reduced their rates of trafficking, although the motif was less potent than the canonical dilysine signal. The dibasic motif bound the coatomer complex I (COPI) in an in vitro binding assay, suggesting that ER retrieval may contribute to the accumulation of SARS CoV S protein near the virus assembly site for interaction with other viral structural proteins. In support of this, we found that the dibasic motif on the SARS S protein was required for its localization to the ERGIC/Golgi region when coexpressed with SARS membrane (M) protein. Thus, the cycling of SARS S through the ER-Golgi system may be required for its incorporation into assembling virions in the ERGIC.
与其他冠状病毒一样,严重急性呼吸综合征冠状病毒(SARS-CoV)在内质网-高尔基体中间区室(ERGIC)的腔中组装并出芽。病毒包膜蛋白在此区室的积累是病毒组装的先决条件。此前,我们报道在SARS-CoV刺突(S)蛋白的细胞质尾巴中鉴定出一个双碱性基序(KxHxx),它类似于典型的双赖氨酸内质网回收信号。在此我们证明,该基序是一种新型的功能性内质网回收信号,它降低了全长S蛋白通过高尔基体复合体的运输速率。KxHxx基序也在内质网-高尔基体中间区室(ERGIC)区域部分保留了两种不同的报告蛋白,并降低了它们的运输速率,尽管该基序的作用不如典型的双赖氨酸信号强。在体外结合试验中,双碱性基序与衣被蛋白复合体I(COPI)结合,这表明内质网回收可能有助于SARS-CoV S蛋白在病毒组装位点附近积累,以便与其他病毒结构蛋白相互作用。支持这一观点的是,我们发现当与SARS膜(M)蛋白共表达时,SARS S蛋白上的双碱性基序是其定位于内质网-高尔基体中间区室(ERGIC)/高尔基体区域所必需的。因此,SARS S蛋白通过内质网-高尔基体系统的循环可能是其整合到内质网-高尔基体中间区室(ERGIC)中正在组装的病毒粒子所必需的。