Lopez P, Van Sant C, Roizman B
The Marjorie B. Kovler Viral Oncology Laboratories, The University of Chicago, Chicago, Illinois 60637, USA.
J Virol. 2001 Apr;75(8):3832-40. doi: 10.1128/JVI.75.8.3832-3840.2001.
Earlier studies have shown that wild-type infected-cell protein 0 (ICP0), a key herpes simplex virus regulatory protein, translocates from the nucleus to the cytoplasm of human embryonic lung (HEL) fibroblasts within several hours after infection (Y. Kawaguchi, R. Bruni, and B. Roizman, J. Virol. 71:1019-1024, 1997). Translocation of ICP0 was also observed in cells infected with the d120 mutant, in which both copies of the gene encoding ICP4, the major regulatory protein, had been deleted (V. Galvan, R. Brandimarti, J. Munger, and B. Roizman, J. Virol. 74:1931-1938, 2000). Furthermore, a mutant (R7914) carrying the D199A substitution in ICP0 does not bind or stabilize cyclin D3 and is retained in the nucleus (C. Van Sant, P. Lopez, S. J. Advani, and B. Roizman, J. Virol. 75:1888-1898, 2001). Studies designed to elucidate the requirements for the translocation of ICP0 between cellular compartments revealed the following. (i) Translocation of ICP0 to the cytoplasm in productive infection maps to the D199 amino acid, inasmuch as wild-type ICP0 delivered in trans to cells infected with an ICP0 null mutant was translocated to the cytoplasm whereas the D199A-substituted mutant ICP0 was not. (ii) Translocation of wild-type ICP0 requires a function expressed late in infection, inasmuch as phosphonoacetate blocked the translocation of ICP0 in wild-type virus-infected cells but not in d120 mutant-infected cells. Moreover, whereas in d120 mutant-infected cells ICP0 was translocated rapidly from the cytoplasm to the nucleus at approximately 5 h after infection, the translocation of ICP0 in wild-type virus-infected cells extended from 5 to at least 9 h after infection. (iii) In wild-type virus-infected cells, the MG132 proteasomal inhibitor blocked the translocation of ICP0 to the cytoplasm early in infection, but when added late in infection, it caused ICP0 to be relocated back to the nucleus from the cytoplasm. (iv) MG132 blocked the translocation of ICP0 in d120 mutant-infected cells early in infection but had no effect on the ICP0 aggregated in vesicle-like structures late in infection. However, in d120 mutant-infected cells treated with MG132 at late times, proteasomes formed a shell-like structure around the aggregated ICP0. These structures were not seen in wild-type virus or R7914 mutant-infected cells. The results indicate the following. (i) In the absence of beta or gamma protein synthesis, ICP0 dynamically associates with proteasomes and is translocated to the cytoplasm. (ii) In cells productively infected beyond alpha gene expression, ICP0 is retained in the nucleus until after the onset of viral DNA synthesis and the synthesis of gamma2 proteins. (iii) Late in infection, ICP0 is actively sequestered in the cytoplasm by a process mediated by proteasomes, inasmuch as interference with proteasomal function causes rapid relocation of ICP0 to the nucleus.
早期研究表明,野生型感染细胞蛋白0(ICP0)是单纯疱疹病毒的一种关键调节蛋白,在感染后数小时内会从人胚肺(HEL)成纤维细胞的细胞核转运至细胞质(Y. Kawaguchi、R. Bruni和B. Roizman,《病毒学杂志》71:1019 - 1024,1997年)。在感染d120突变体的细胞中也观察到了ICP0的转运,该突变体中编码主要调节蛋白ICP4的两个基因拷贝均已缺失(V. Galvan、R. Brandimarti、J. Munger和B. Roizman,《病毒学杂志》74:1931 - 1938,2000年)。此外,在ICP0中携带D199A替换的突变体(R7914)不结合或稳定细胞周期蛋白D3,并保留在细胞核中(C. Van Sant、P. Lopez、S. J. Advani和B. Roizman,《病毒学杂志》75:1888 - 1898,2001年)。旨在阐明ICP0在细胞区室间转运所需条件的研究揭示了以下几点。(i)在生产性感染中,ICP0向细胞质的转运定位于第199位氨基酸,因为反式导入感染ICP0缺失突变体的细胞中的野生型ICP0会转运至细胞质,而D199A替换的突变体ICP0则不会。(ii)野生型ICP0的转运需要感染后期表达的一种功能,因为膦甲酸可阻断野生型病毒感染细胞中ICP0的转运,但对d120突变体感染的细胞则无此作用。此外,在d120突变体感染的细胞中,ICP0在感染后约5小时迅速从细胞质转运至细胞核,而在野生型病毒感染的细胞中,ICP0的转运从感染后5小时持续至至少9小时。(iii)在野生型病毒感染的细胞中,MG132蛋白酶体抑制剂在感染早期可阻断ICP0向细胞质的转运,但在感染后期添加时,它会使ICP0从细胞质重新定位回细胞核。(iv)MG132在感染早期可阻断d120突变体感染细胞中ICP0的转运,但对感染后期聚集在囊泡样结构中的ICP0无影响。然而,在感染后期用MG132处理的d120突变体感染细胞中,蛋白酶体在聚集的ICP0周围形成壳样结构。在野生型病毒或R7914突变体感染的细胞中未见到这些结构。结果表明以下几点。(i)在缺乏β或γ蛋白合成的情况下,ICP0与蛋白酶体动态结合并转运至细胞质。(ii)在α基因表达之后进行生产性感染的细胞中,ICP0保留在细胞核中,直至病毒DNA合成开始和γ2蛋白合成之后。(iii)在感染后期,ICP0通过蛋白酶体介导的过程被主动隔离在细胞质中,因为对蛋白酶体功能的干扰会导致ICP0迅速重新定位至细胞核。