Martelli A M, Capitani S, Neri L M
Dipartimento di Morfologia Umana Normale, Università di Trieste, Italy.
J Cell Biochem. 1998 Oct 1;71(1):11-20. doi: 10.1002/(sici)1097-4644(19981001)71:1<11::aid-jcb2>3.0.co;2-4.
We investigated the association of DNA polymerase and DNA primase activity with the nuclear matrix in HeLa S3 cells diluted with fresh medium after having been cultured without any medium change for 7 days. Flow cytometric analysis demonstrated that just before dilution about 85% of the cells were in the G1 phase of the cycle, whereas 8% were in the S phase. After dilution with fresh medium, 18-22 h were required for the cell population to attain a stable distribution with respect to the cell cycle. At that time, about 38% of the cells were in the S phase. DNA polymerase and DNA primase activity associated with the nuclear matrix prepared from cells just before dilution represented about 10% of nuclear activity. As judged by [3H]-thymidine incorporation and flow cytometric analysis, an increase in the number of S-phase cells was evident at least 6 h after dilution. However, as early as 2 h after dilution into fresh medium, a striking prereplicative increase of the two activities was seen in the nuclear matrix fraction but not in cytosol or isolated nuclei. Both DNA polymerase and primase activities bound to the matrix were about 60% of nuclear activity. Overall, the nuclear matrix was the cell fraction where the highest induction (about 10-fold) of both enzymatic activities was seen at 30 h after dilution, whereas in cytosol and isolated nuclei the increase was about two- and fourfold, respectively. Typical immunofluorescent patterns given by an antibody to 5-bromodeoxyuridine were seen after dilution. These findings, which are at variance with our own previous results obtained with cell cultures synchronized by either a double thymidine block or aphidicolin exposure, strengthen the contention that DNA replication is associated with an underlying nuclear structure and demonstrate the artifacts that may be generated by procedures commonly used to synchronize cell cultures.
我们研究了在无培养基更换条件下培养7天后,用新鲜培养基稀释的HeLa S3细胞中DNA聚合酶和DNA引发酶活性与核基质的关联。流式细胞术分析表明,在稀释前约85%的细胞处于细胞周期的G1期,而8%处于S期。用新鲜培养基稀释后,细胞群体需要18 - 22小时才能在细胞周期方面达到稳定分布。此时,约38%的细胞处于S期。与稀释前细胞制备的核基质相关的DNA聚合酶和DNA引发酶活性约占核活性的10%。通过[3H] - 胸腺嘧啶核苷掺入和流式细胞术分析判断,稀释后至少6小时S期细胞数量明显增加。然而,早在稀释到新鲜培养基后2小时,在核基质部分就观察到这两种活性显著的复制前增加,而在胞质溶胶或分离的细胞核中未观察到。与基质结合的DNA聚合酶和引发酶活性均约为核活性的60%。总体而言,核基质是在稀释后30小时两种酶活性诱导最高(约10倍)的细胞部分,而在胞质溶胶和分离的细胞核中增加分别约为两倍和四倍。稀释后可见抗5 - 溴脱氧尿苷抗体给出的典型免疫荧光模式。这些发现与我们之前通过双胸腺嘧啶阻断或阿非迪霉素处理同步化细胞培养所获得的结果不同,强化了DNA复制与潜在核结构相关的观点,并证明了常用于同步化细胞培养的程序可能产生的假象。