Schwartz S A, Panem S, Kirsten W H
Proc Natl Acad Sci U S A. 1975 May;72(5):1829-33. doi: 10.1073/pnas.72.5.1829.
Rat embryo cell cultures were synchronized by a double thymidine block. The DNA replication phase (S) was divided into an early, middle, and late period. Cell cultures in the early, middle, or late S phase were pulsed with 0.1 muM 5-bromo[(3)H]deoxyuridine (BrdU) or equimolar [(3)H]dT. DNA-DNA reassociation experiments of each sample revealed that [(3)H]BrdU was more concentrated in the intermediate repetitive than the repetitive or unique DNA sequences of the early and middle S phase. In contrast, [(3)H]dT was nearly uniformly jistributed throughout all nucleotide sequences during the entire S phase. synchronized rat cells were pulsed during various portions of the S phase with unlabeled 0.1 mM or 0.1 muM BrdU and examined for sytoplasmic immumofluorescence against the 30,000 molecular weight group-specific antigen (p30) of Friend mouse leukemia virus. Equally strong fluorescence was detected 12 hr later in cells treated with each concentration of BrdU. Furthermore, incorporation of BrdU during late S phase was suffieient to elicit maximal antigen expression.
大鼠胚胎细胞培养物通过双胸腺嘧啶核苷阻断进行同步化处理。DNA复制期(S期)被分为早期、中期和晚期。处于S期早期、中期或晚期的细胞培养物用0.1μM 5-溴[(3)H]脱氧尿苷(BrdU)或等摩尔的[(3)H]dT进行脉冲标记。每个样品的DNA-DNA重结合实验表明,在S期早期和中期,[(3)H]BrdU在中度重复DNA序列中的浓度高于在重复或单一DNA序列中的浓度。相比之下,在整个S期,[(3)H]dT几乎均匀地分布于所有核苷酸序列中。在S期的不同时间段,用未标记的0.1mM或0.1μM BrdU对同步化的大鼠细胞进行脉冲标记,并检测针对弗氏小鼠白血病病毒30,000分子量组特异性抗原(p30)的细胞质免疫荧光。12小时后,在用每种浓度BrdU处理的细胞中检测到同样强烈的荧光。此外,在S期晚期掺入BrdU足以引发最大程度的抗原表达。