Welsch Sonja, Doglio Laura, Schleich Sibylle, Krijnse Locker Jacomine
European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
J Virol. 2003 May;77(10):6014-28. doi: 10.1128/jvi.77.10.6014-6028.2003.
The vaccinia virus (VV) I3L gene product is a single-stranded DNA-binding protein made early in infection that localizes to the cytoplasmic sites of viral DNA replication (S. C. Rochester and P. Traktman, J. Virol. 72:2917-2926, 1998). Surprisingly, when replication was blocked, the protein localized to distinct cytoplasmic spots (A. Domi and G. Beaud, J. Gen. Virol. 81:1231-1235, 2000). Here these I3L-positive spots were characterized in more detail. By using an anti-I3L peptide antibody we confirmed that the protein localized to the cytoplasmic sites of viral DNA replication by both immunofluorescence and electron microscopy (EM). Before replication had started or when replication was inhibited with hydroxyurea or cytosine arabinoside, I3L localized to distinct cytoplasmic punctate structures of homogeneous size. We show that these structures are not incoming cores or cytoplasmic sites of VV early mRNA accumulation. Instead, morphological and quantitative data indicate that they are specialized sites where the parental DNA accumulates after its release from incoming viral cores. By EM, these sites appeared as complex, electron-dense structures that were intimately associated with the cellular endoplasmic reticulum (ER). By double labeling of cryosections we show that they contain DNA and a viral early protein, the gene product of E8R. Since E8R is a membrane protein that is able to bind to DNA, the localization of this protein to the I3L puncta suggests that they are composed of membranes. The results are discussed in relation to our previous data showing that the process of viral DNA replication also occurs in close association with the ER.
痘苗病毒(VV)I3L基因产物是一种在感染早期产生的单链DNA结合蛋白,定位于病毒DNA复制的细胞质位点(S.C.罗切斯特和P.特拉特曼,《病毒学杂志》72:2917 - 2926,1998年)。令人惊讶的是,当复制被阻断时,该蛋白定位于不同的细胞质斑点(A.多米和G.博德,《普通病毒学杂志》81:1231 - 1235,2000年)。在此对这些I3L阳性斑点进行了更详细的表征。通过使用抗I3L肽抗体,我们通过免疫荧光和电子显微镜(EM)证实该蛋白定位于病毒DNA复制的细胞质位点。在复制开始之前或当用羟基脲或阿糖胞苷抑制复制时,I3L定位于大小均匀的不同细胞质点状结构。我们表明这些结构不是进入的核心或VV早期mRNA积累的细胞质位点。相反,形态学和定量数据表明它们是亲代DNA从进入的病毒核心释放后积累的特化位点。通过EM,这些位点表现为复杂的、电子致密的结构,与细胞内质网(ER)紧密相关。通过对冷冻切片进行双重标记,我们表明它们含有DNA和一种病毒早期蛋白,即E8R的基因产物。由于E8R是一种能够与DNA结合的膜蛋白,该蛋白在I3L斑点中的定位表明它们由膜组成。结合我们之前的数据讨论了这些结果,之前的数据表明病毒DNA复制过程也与内质网密切相关。