Pinard M F, Simard R, Bibor-Hardy V
J Gen Virol. 1987 Mar;68 ( Pt 3):727-35. doi: 10.1099/0022-1317-68-3-727.
The nuclear matrix is involved in the replicative cycle of herpes simplex virus type 1 (HSV-1) and in at least some cases viral DNA has been shown to be closely associated with this structure. In this communication, we report the presence of five DNA-binding proteins in the nuclear matrix of HSV-1-infected BHK cells. These proteins (p114, p89, p77, p37 and p29) were detected by probing with 32P-labelled HSV DNA after Western blotting of nuclear matrix proteins. Three were identified as virion components: p89 as VP12, p77 as VP13 and p37 as the capsid protein VP22a. These polypeptides were detected in cells and nuclei and found to be associated with the nuclear matrix late during the lytic cycle, long after the onset of viral DNA replication. The nuclear matrix-binding capacity of VP22a depended on viral DNA replication, since after DNA polymerase inhibition it was still synthesized and transported into the nucleus but was no longer associated with the nuclear matrix. After inhibition of viral DNA synthesis, VP13 was no longer found in cells, nuclei or nuclear matrices. These results suggest a possible involvement in anchoring viral progeny DNA to the nuclear matrix.
核基质参与单纯疱疹病毒1型(HSV - 1)的复制周期,并且在至少某些情况下,病毒DNA已被证明与该结构紧密相关。在本通讯中,我们报道了在HSV - 1感染的BHK细胞的核基质中存在五种DNA结合蛋白。在对核基质蛋白进行蛋白质印迹分析后,用32P标记的HSV DNA进行探测,检测到了这些蛋白质(p114、p89、p77、p37和p29)。其中三种被鉴定为病毒体成分:p89为VP12,p77为VP13,p37为衣壳蛋白VP22a。这些多肽在细胞和细胞核中被检测到,并发现它们在裂解周期后期,即病毒DNA复制开始很久之后,与核基质相关联。VP22a的核基质结合能力取决于病毒DNA复制,因为在DNA聚合酶受到抑制后,它仍能合成并转运到细胞核中,但不再与核基质相关联。在抑制病毒DNA合成后,在细胞、细胞核或核基质中均未再发现VP13。这些结果表明,它们可能参与将病毒子代DNA锚定到核基质中。