Tatsumi K, Strauss B
Nucleic Acids Res. 1978 Feb;5(2):331-47. doi: 10.1093/nar/5.2.331.
Incubation of human lymphoid cells with bromodeoxyuridine (BrdUrd) for short periods produces three classes of DNA containing analog: DNAHL (hybrid DNA, density approximately equal to 1.75 g/cm3), DNAint (intermediate density DNA, density approximately equal to 1.71 g/cm3), and DNAHH (DNA with both strands containing analog, density approximately equal to 1.80 g/cm3). Preparations of DNAint yield DNAHH after extensive shearing and/or treatment with single strand specific endonuclease. Cross-linking of pulse-labeled (BrdUrd + 3HdT) DNA in cells by treatment with trioxsalen and near UV light before lysis prevents the appearance of DNAHH.Cross-linking after lysis has little effect. A large fraction of DNAHH is obtained after incubation of cells with caffeine. Extraction of DNA at high salt concentration or cross-linking with trioxsalen and near UV light drastically reduced the amount of DNAHH obtained from caffeine-treated cells. We conclude that most DNAHH arises from in vitro branch migration in isolated DNA growing points.
用人淋巴细胞与溴脱氧尿苷(BrdUrd)短期温育可产生三类含类似物的DNA:DNAHL(杂交DNA,密度约等于1.75 g/cm³)、DNAint(中等密度DNA,密度约等于1.71 g/cm³)和DNAHH(两条链均含类似物的DNA,密度约等于1.80 g/cm³)。DNAint制剂在经过广泛剪切和/或用单链特异性内切酶处理后会产生DNAHH。在裂解前用三甲沙林和近紫外光处理细胞,使脉冲标记(BrdUrd + ³HdT)DNA交联,可防止DNAHH出现。裂解后交联影响很小。细胞用咖啡因温育后可获得大部分DNAHH。在高盐浓度下提取DNA或用三甲沙林和近紫外光交联,会大幅减少从咖啡因处理的细胞中获得的DNAHH量。我们得出结论,大多数DNAHH源自分离的DNA生长点中的体外分支迁移。