Nagarajan M, Johnson L F
Department of Biochemistry, Ohio State University, Columbus 43210.
Exp Cell Res. 1989 Mar;181(1):289-97. doi: 10.1016/0014-4827(89)90203-6.
Previous studies have shown that thymidylate synthase gene expression is regulated over a wide range in response to growth stimulation in cultured mouse fibroblasts. In the present study we show that the gene is also regulated during the cell cycle in continuously growing cells. Our analyses were conducted with a fluorodeoxyuridine-resistant mouse 3T6 cell line that overproduces thymidylate synthase and its mRNA by a factor of 50 due to gene amplification. Cells were synchronized by mitotic selection. RNA blot analyses showed that the amount of thymidylate synthase mRNA increased 5- to 10-fold as cells progressed from G1 through the middle of S phase. S1 nuclease protection assays showed that the pattern of 5' termini of thymidylate synthase mRNA was the same in G1 and S phase. Despite the large increase in thymidylate synthase mRNA content, the level of the enzyme increased only by a factor of 2 as cells progressed from G1 to mid S phase. This apparent discrepancy can be explained by the fact that the enzyme is highly stable.
以往的研究表明,在培养的小鼠成纤维细胞中,胸苷酸合成酶基因的表达会随着生长刺激在很宽的范围内受到调控。在本研究中,我们发现该基因在连续生长的细胞的细胞周期中也受到调控。我们使用了一种对氟脱氧尿苷耐药的小鼠3T6细胞系进行分析,由于基因扩增,该细胞系产生的胸苷酸合成酶及其mRNA比正常水平高50倍。通过有丝分裂选择使细胞同步化。RNA印迹分析表明,随着细胞从G1期进入S期中期,胸苷酸合成酶mRNA的量增加了5至10倍。S1核酸酶保护试验表明,胸苷酸合成酶mRNA的5'末端模式在G1期和S期是相同的。尽管胸苷酸合成酶mRNA含量大幅增加,但随着细胞从G1期进入S期中期,该酶的水平仅增加了2倍。这种明显的差异可以用该酶高度稳定这一事实来解释。