Manso-Martínez R, Avila J
Mol Cell Biochem. 1978 Aug 16;20(3):183-9. doi: 10.1007/BF00243765.
BHK21/Cl1 cells, starved for 30 h in serum deficient medium and treated for 15 h with 1 mM hydroxyorea (HO) in order to obtain a synchronous cell population in the G1/S-boundary, incorporate a residual proportion of 3H-thymidine (dThd). This residual incorporation is due to semiconservative synthesis and may not be reduced by increasing the drug concentration without affecting the reversion capacity of the cells proportionally. As shown by autoradiographic analysis, the residual DNA synthesis does not correspond to 3H-dThd incorporation within a small number of resistant cells, but is located in the nuclei of a high proportion of cells with reduced density of silver grains. After treatment with 0.05 mM HU, however, the incorporation of 3H-dThd increases considerably over the control values. The determination of the radioactivity incorporated by microgram DNA corresponding to nuclei in S phase indicates that this concentration of HU is also able to reduce the rate of DNA polymerization. Kinetic data on the appearance of this increased 3H-dThd incorporation and on the accumulation of labelled nuclei in cells growing at random and labelled continuously with the radioactive DNA precursor indicate that HU stimulates the cells to enter the S phase. The reported results are consistent with a mechanism of action of HU which affects initiation and elongation of DNA chains separately.
将BHK21/Cl1细胞在无血清培养基中饥饿培养30小时,并用1 mM羟基脲(HO)处理15小时,以获得处于G1/S边界的同步细胞群体,该细胞群体掺入了残留比例的3H-胸腺嘧啶核苷(dThd)。这种残留掺入是由于半保留合成所致,在不按比例影响细胞回复能力的情况下,增加药物浓度可能无法降低这种残留掺入。放射自显影分析表明,残留的DNA合成并非对应于少数抗性细胞内的3H-dThd掺入,而是位于银颗粒密度降低的高比例细胞的细胞核中。然而,用0.05 mM羟基脲(HU)处理后,3H-dThd的掺入量比对照值大幅增加。对处于S期的细胞核中每微克DNA掺入的放射性进行测定表明,该浓度的HU也能够降低DNA聚合速率。关于这种增加的3H-dThd掺入的出现以及在随机生长并用放射性DNA前体持续标记的细胞中标记细胞核积累的动力学数据表明,HU刺激细胞进入S期。所报道的结果与HU的作用机制一致,即HU分别影响DNA链的起始和延伸。