Scarano F J, Laffin J A, Lehman J M, Friedrich T D
Department of Microbiology, Immunology, and Molecular Genetics, Albany Medical College, New York 12208.
J Virol. 1994 Apr;68(4):2355-61. doi: 10.1128/JVI.68.4.2355-2361.1994.
Simian virus 40 (SV40) infection stimulates confluent cultures of monkey kidney cells into successive rounds of cellular DNA synthesis without intervening mitosis. As an initial step in defining the mechanisms responsible for viral inhibition of mitosis, M-phase-promoting factor (MPF) was examined in SV40-infected CV-1 cells passing from G2 phase into a second S phase. MPF is a serine-threonine protein kinase that is essential for mitosis in eukaryotic cells. In SV40-infected cells exiting G2 phase, there was a reduced amount of MPF-associated H1 kinase activity relative to that of uninfected cells passing through mitosis. Both subunits of MPF, cyclin B and the p34cdc2 catalytic subunit, were present and in a complex in infected cells. In uninfected cultures, passage through mitosis was associated with the dephosphorylation of the p34cdc2 subunit, which is characteristic of MPF activation. In contrast, the p34cdc2 subunit remained in the tyrosine-phosphorylated, inactive form in SV40-infected cells passing from G2 phase into a second S phase. These results suggest that although the MPF complex is assembled and modified normally, SV40 interferes with pathways leading to MPF activation.
猿猴病毒40(SV40)感染可刺激猴肾细胞的汇合培养物进入连续的细胞DNA合成轮次,而无需进行有丝分裂。作为确定病毒抑制有丝分裂机制的第一步,我们在从G2期进入第二个S期的SV40感染的CV-1细胞中检测了M期促进因子(MPF)。MPF是一种丝氨酸 - 苏氨酸蛋白激酶,对真核细胞的有丝分裂至关重要。在退出G2期的SV40感染细胞中,相对于通过有丝分裂的未感染细胞,MPF相关的H1激酶活性降低。MPF的两个亚基,细胞周期蛋白B和p34cdc2催化亚基,在感染细胞中均存在且形成复合物。在未感染的培养物中,通过有丝分裂与p34cdc2亚基的去磷酸化有关,这是MPF激活的特征。相比之下,在从G2期进入第二个S期的SV40感染细胞中,p34cdc2亚基保持酪氨酸磷酸化的无活性形式。这些结果表明,尽管MPF复合物正常组装和修饰,但SV40会干扰导致MPF激活的途径。