Cohen S M, Cobb E R, Cordeiro-Stone M, Kaufman D G
Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, 27599-7525, USA.
Exp Cell Res. 1998 Dec 15;245(2):321-9. doi: 10.1006/excr.1998.4258.
Normal human fibroblasts (NHF1) were released from confluence arrest (G0) and replated in medium containing bromodeoxyuridine (BrdU) and aphidicolin. Despite severe reduction in the rate of DNA synthesis by aphidicolin, cells reentering the cell cycle incorporated BrdU at regions of the human genome that replicated very early in S phase. After removal of aphidicolin and BrdU from the tissue culture medium, cells were collected in mitosis. Q-banding with 4', 6-diamidino-2-phenylindole/actinomycin D was used to identify metaphase chromosomes. A monoclonal anti-BrdU antibody and a fluorescein isothiocyanate (FITC)-conjugated goat anti-mouse antibody were used to identify the BrdU-labeled sites. The criterion for scoring DNA replication sites was the detection of FITC fluorescence at homologous regions of both sister chromatids. Early replicating regions mapped within R-bands, but not all R-bands incorporated BrdU. Chromosomal bands 1p36.1, 8q24.1, 12q13, 15q15, 15q22, and 22q13 were labeled in 53% or more of the copies of these chromosomes in the data set, suggesting that these sites replicated very early in S phase. Chromosomal band 15q22 was the most frequently labeled site (64%), which indicates that it contains some of the earliest replicating sequences in normal human fibroblasts.
将正常人类成纤维细胞(NHF1)从汇合停滞(G0期)中释放出来,并重新接种到含有溴脱氧尿苷(BrdU)和阿非迪霉素的培养基中。尽管阿非迪霉素使DNA合成速率大幅降低,但重新进入细胞周期的细胞在人类基因组中S期非常早期复制的区域掺入了BrdU。从组织培养基中去除阿非迪霉素和BrdU后,收集处于有丝分裂期的细胞。使用4',6-二脒基-2-苯基吲哚/放线菌素D进行Q带分析以鉴定中期染色体。使用单克隆抗BrdU抗体和异硫氰酸荧光素(FITC)偶联的山羊抗小鼠抗体来鉴定BrdU标记的位点。对DNA复制位点进行评分的标准是在两条姐妹染色单体的同源区域检测到FITC荧光。早期复制区域定位于R带内,但并非所有R带都掺入了BrdU。在数据集中,染色体带1p36.1、8q24.1、12q13、15q15、15q22和22q13在这些染色体的53%或更多拷贝中被标记,这表明这些位点在S期非常早期进行复制。染色体带15q22是最常被标记的位点(64%),这表明它包含正常人类成纤维细胞中一些最早的复制序列。