Wolgemuth D J, Biedler J L, Melera P W
Biochem Genet. 1980 Aug;18(7-8):655-67. doi: 10.1007/BF00484583.
DNA purified from a Chinese hamster cell line of lung fibroblast origin (DC83F) was analyzed by density gradient centrifugation and by gel electrophoresis after restriction endonuclease digestion in order to fractionate discrete repetitive fractions within the total DNA. No obvious satellite DNAs were resolved using the CsCl or Ag-Cs2SO4 density gradient conditions described herein. However, analysis of the digestion products of a battery of restriction endonucleases indicated that three of these enzymes, EcoR1, HaeIII, and XhoI, yielded discrete fragments which could be visualized with EtBr staining or identified by scintillation counting of [3H]DNA. DNAs from several highly (greater than or equal to hundredfold increased resistance) antifolate-resistant sublines of DC-3F, characterized by a large homogeneously staining region (HSR) in the chromosome complement, were examined with both techniques and compared to the parental, antifolate-sensitive cell line DNA. The density gradient profiles and electrophoretic patterns of restriction endonuclease digests were identical among all the cell lines examined and were indistinguishable from those of the parental DC-3F DNA.
为了分离总DNA中离散的重复片段,对源自中国仓鼠肺成纤维细胞系(DC83F)的纯化DNA进行了密度梯度离心分析,并在限制性内切酶消化后进行了凝胶电泳分析。使用本文所述的CsCl或Ag-Cs2SO4密度梯度条件,未分辨出明显的卫星DNA。然而,对一系列限制性内切酶的消化产物进行分析表明,其中三种酶EcoR1、HaeIII和XhoI产生了离散的片段,这些片段可用溴化乙锭染色可视化,或通过对[3H]DNA进行闪烁计数来鉴定。用这两种技术检测了DC-3F的几个高度(大于或等于百倍增加抗性)抗叶酸亚系的DNA,这些亚系的特征是染色体组中有一个大的均匀染色区(HSR),并与亲本抗叶酸敏感细胞系DNA进行了比较。在所检测的所有细胞系中,限制性内切酶消化产物的密度梯度图谱和电泳图谱是相同的,与亲本DC-3F DNA的图谱无法区分。