Scott F W, Forsdyke D R
Biochem J. 1978 Mar 15;170(3):545-9. doi: 10.1042/bj1700545.
The rate of DNA synthesis is exponentially growing cells was determined by isotopedilution analysis of the incorporation of [me-3H]thymidine. Thymidine concentrations greater than 7 micrometer were used so that the rate-limiting step governing incorporation would be at the level of DNA polymerase rather than at the level of thymidine kinase [Sjostrom & Forsdyke (1974) Biochem. J. 138, 253-262]. In early exponential phase the rate determined by isotope-dilution analysis closely correlated with the rates calculated either from growth curves or from known cell-cycle parameters. However, in late-exponential phase the rate calculated from the growth curve was less than that determined by isotope-dilution analysis. We conclude that, under certain conditions, the pool-corrected rate of incorporation of [me-3H]thymidine, as determined by isotope-dilution analysis, can accurately reflect the rate of DNA synthesis. Discrepancies between the observed rate of DNA synthesis and increase in cell number could reflect an exponential degeneration of post-S-phase cells.
通过对[甲基-³H]胸腺嘧啶核苷掺入的同位素稀释分析,测定指数生长细胞中的DNA合成速率。使用大于7微摩尔的胸腺嘧啶核苷浓度,以便控制掺入的限速步骤处于DNA聚合酶水平而非胸腺嘧啶激酶水平[Sjostrom和Forsdyke(1974年),《生物化学杂志》138卷,253 - 262页]。在指数生长早期,同位素稀释分析测定的速率与根据生长曲线或已知细胞周期参数计算出的速率密切相关。然而,在指数生长后期,根据生长曲线计算出的速率低于同位素稀释分析测定的速率。我们得出结论,在某些条件下,通过同位素稀释分析测定的经库校正的[甲基-³H]胸腺嘧啶核苷掺入速率能够准确反映DNA合成速率。观察到的DNA合成速率与细胞数量增加之间的差异可能反映了S期后细胞的指数性退化。