Lynn S, Yew F H, Jan K Y
Department of Zoology, National Taiwan University, Taipei.
Biol Trace Elem Res. 1997 Winter;59(1-3):1-11. doi: 10.1007/BF02783224.
The activities of DNA polymerization and DNA ligation in extract of Chinese hamster ovary cells were both stimulated by MgCl2. DNA polymerization was stimulated by MgCl2 above 0.25 mM, whereas, MgCl2 above 2 mM was required to stimulate DNA ligation. The activity of DNA polymerization maintained a plateau at MgCl2 1-12 mM, whereas DNA ligation reached a maximal activity at MgCl2 6 mM and decreased thereafter. NiCl2 0.1-0.2 mM also had a stimulatory effect on DNA polymerization, but was much less potent than MgCl2. However, nickel ion (Ni2+) had no detectable stimulating effect on the activity of DNA ligation. In the presence of MgCl2, the activities of DNA polymerization and DNA ligation decreased with increasing concentration of NiCl2. Ni2+ inhibition of DNA polymerization was reduced by increasing the concentration of MgCl2, but increasing the concentration of MgCl2 did not reduce Ni2+ inhibition of DNA ligation. Preincubating cell extract with MgCl2 decreased the Ni2+ inhibition of DNA polymerization but not DNA ligation. These results suggest that Ni2+ may compete with magnesium ion (Mg2+) to reduce DNA polymerization, but this mechanism seems not applicable to Ni2+ inhibition of DNA ligation.
氯化镁可刺激中国仓鼠卵巢细胞提取物中的DNA聚合活性和DNA连接活性。当氯化镁浓度高于0.25 mM时可刺激DNA聚合,而刺激DNA连接则需要氯化镁浓度高于2 mM。在氯化镁浓度为1 - 12 mM时,DNA聚合活性保持平稳,而DNA连接在氯化镁浓度为6 mM时达到最大活性,之后下降。0.1 - 0.2 mM的氯化镍对DNA聚合也有刺激作用,但效力远低于氯化镁。然而,镍离子(Ni2+)对DNA连接活性没有可检测到的刺激作用。在存在氯化镁的情况下,DNA聚合和DNA连接活性随氯化镍浓度增加而降低。通过增加氯化镁浓度可减轻Ni2+对DNA聚合的抑制作用,但增加氯化镁浓度并不能减轻Ni2+对DNA连接的抑制作用。用氯化镁对细胞提取物进行预孵育可减轻Ni2+对DNA聚合的抑制作用,但不能减轻对DNA连接的抑制作用。这些结果表明,Ni2+可能与镁离子(Mg2+)竞争以降低DNA聚合,但这种机制似乎不适用于Ni2+对DNA连接的抑制作用