Ciufo D M, Mullen M A, Hayward G S
Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Virol. 1994 May;68(5):3267-82. doi: 10.1128/JVI.68.5.3267-3282.1994.
The 775-amino-acid IE110 (or ICP0) phosphoprotein of herpes simplex virus (HSV) functions as an accessory transcription factor during the lytic cycle and plays a critical role in reactivation from latent infection. By immunofluorescence analysis, IE110 localizes in a novel pattern consisting of several dozen spherical punctate granules in the nuclei of DNA-transfected cells. We constructed a hybrid version of IE110 that contained an epitope-tagged domain from the N terminus of the HSV IE175 protein and lacked the IE110 N-terminal domain that confers punctate characteristics. This hybrid IE175(N)/IE110(C) protein gave an irregular nuclear diffuse pattern on its own but was redistributed very efficiently into spherical punctate granules after cotransfection with the wild-type HSV-1 IE110 protein. Similar colocalization interactions occurred with internally deleted forms of IE110 that lacked the zinc finger region or large segments from the center of the protein, including both cytoplasmic and elongated punctate forms, but C-terminal truncated versions of IE110 did not interact. In all such interactions, the punctate phenotype was dominant. Evidence that C-terminal segments of IE110 could also form stable mixed-subunit oligomers in vitro was obtained by coimmunoprecipitation of in vitro-translated IE110 polypeptides with different-size hemagglutinin epitope-tagged forms of the protein. This occurred only when the two forms were cotranslated, not when they were simply mixed together. An in vitro-synthesized IE110 C-terminal polypeptide also gave immunoprecipitable homodimers and heterodimers when two different-size forms were cross-linked with glutaraldehyde and reacted specifically with a bacterial glutathione S-transferase/IE110 C-terminal protein in far-Western blotting experiments. The use of various N-terminal and C-terminal truncated forms of IE110 in the in vivo assays revealed that the outer boundaries of the interaction domain mapped between codons 617 and 711, although inclusion of adjacent codons on either side increased the efficiency severalfold in some assays. We conclude that the C-terminal region of IE110 contains a high-affinity self-interaction domain that leads to stable dimer and higher-order complex formation both in DNA-transfected cells and in in vitro assays. This segment of IE110 is highly conserved between HSV-1 and HSV-2 and appears to have the potential to play an important role in the interaction with the IE175 protein, as well as in correct intracellular localization, but it is not present in the equivalent proteins from varicella-zoster virus, pseudorabies virus, or equine abortion virus.
单纯疱疹病毒(HSV)的775个氨基酸的IE110(或ICP0)磷蛋白在裂解周期中作为辅助转录因子发挥作用,并且在潜伏感染的激活过程中起关键作用。通过免疫荧光分析,IE110以一种新模式定位,该模式由DNA转染细胞细胞核中的几十种球形点状颗粒组成。我们构建了一个IE110的杂交版本,它包含来自HSV IE175蛋白N端的一个表位标签结构域,并且缺少赋予点状特征的IE110 N端结构域。这种杂交的IE175(N)/IE110(C)蛋白自身呈现不规则的核弥漫模式,但在与野生型HSV-1 IE110蛋白共转染后能非常有效地重新分布到球形点状颗粒中。与IE110的内部缺失形式也发生了类似的共定位相互作用,这些缺失形式缺少锌指区域或蛋白中心的大片段,包括细胞质和细长点状形式,但IE110的C端截短版本没有相互作用。在所有这些相互作用中,点状表型是显性的。通过体外翻译的IE110多肽与不同大小的血凝素表位标签形式的蛋白进行共免疫沉淀,获得了IE110的C端片段在体外也能形成稳定的混合亚基寡聚体的证据。这仅在两种形式共同翻译时发生,而不是简单地混合在一起时发生。当两种不同大小形式的体外合成的IE110 C端多肽用戊二醛交联并在远缘杂交印迹实验中与细菌谷胱甘肽S-转移酶/IE110 C端蛋白特异性反应时,也产生了可免疫沉淀的同二聚体和异二聚体。在体内实验中使用各种N端和C端截短形式的IE110表明,相互作用结构域的外部边界定位在密码子617和711之间,尽管在某些实验中两侧包含相邻密码子会使效率提高几倍。我们得出结论,IE110的C端区域包含一个高亲和力的自我相互作用结构域,该结构域在DNA转染细胞和体外实验中都能导致稳定的二聚体和高阶复合物形成。IE110的这一区域在HSV-1和HSV-2之间高度保守,似乎有可能在与IE175蛋白的相互作用以及正确的细胞内定位中发挥重要作用,但水痘带状疱疹病毒、伪狂犬病病毒或马流产病毒的等效蛋白中不存在该区域。