Koza R A, Herbst E J
Department of Biochemistry, University of New Hampshire, Durham, NH 03824.
Biochem J. 1992 Jan 1;281 ( Pt 1)(Pt 1):87-93. doi: 10.1042/bj2810087.
Synchronized HeLa cells depleted of polyamines by alpha-difluoromethylornithine exhibited substantially decreased DNA synthesis, and proliferation ceased after the release of the cells into S phase. Nuclei from these cells synthesized 70-80% less DNA than did nuclei from control cells. Extraction of isolated nuclei with 0.3 M-KCl decreased DNA synthesis by about 60%, which was recovered almost completely in control cell nuclei by reconstitution with the salt extracts of these nuclei. On the other hand, salt extracts of polyamine-depleted nuclei restored only 50% of DNA synthesis in extracted control nuclei. Salt extracts of control cell nuclei contained twice the DNA polymerase alpha activity of polyamine-depleted nuclear extracts. Extracts of cell lysates of both control and polyamine-depleted HeLa cells exhibited similar DNA polymerase alpha activity, suggesting that uptake of the enzyme or its retention by the nuclei of polyamine-depleted cells was decreased. Polyamine-depleted nuclei also showed altered phosphorylation of a 31 kDa protein as compared with control nuclei. Almost normal DNA synthesis, cell proliferation, DNA polymerase alpha activity and nuclear protein phosphorylation were restored in polyamine-depleted cells grown in medium supplemented with 20 microM-spermidine at least 10-12 h before S phase. Cultures in which proliferation was blocked by alpha-difluoromethylornithine did not exhibit synchronous growth after the block was removed. Thus it may be concluded that HeLa cells depleted of polyamines are not inhibited at a single control point in the cell cycle, but are arrested at diverse sites throughout G1 phase.
用α-二氟甲基鸟氨酸使多胺耗竭的同步化HeLa细胞显示DNA合成显著减少,并且在细胞进入S期后增殖停止。这些细胞的细胞核合成的DNA比对照细胞核少70 - 80%。用0.3M - KCl提取分离的细胞核使DNA合成减少约60%,通过用这些细胞核的盐提取物重建,对照细胞核中的DNA合成几乎完全恢复。另一方面,多胺耗竭细胞核的盐提取物仅能恢复提取的对照细胞核中50%的DNA合成。对照细胞核的盐提取物中DNA聚合酶α活性是多胺耗竭细胞核提取物的两倍。对照和多胺耗竭的HeLa细胞裂解物提取物显示出相似的DNA聚合酶α活性,这表明多胺耗竭细胞的细胞核对该酶的摄取或保留减少。与对照细胞核相比,多胺耗竭的细胞核还显示出31kDa蛋白的磷酸化改变。在S期前至少10 - 12小时在补充有20μM亚精胺的培养基中生长的多胺耗竭细胞中,几乎恢复了正常的DNA合成、细胞增殖、DNA聚合酶α活性和核蛋白磷酸化。用α-二氟甲基鸟氨酸阻断增殖的培养物在阻断解除后未表现出同步生长。因此可以得出结论,多胺耗竭的HeLa细胞并非在细胞周期的单个控制点受到抑制,而是在整个G1期的不同位点被阻滞。