Beattie K L
Biophys J. 1972 Nov;12(11):1573-82. doi: 10.1016/S0006-3495(72)86183-6.
Haemophilus influenzae was labeled with thymidine-(3)H (dThd), then grown in the presence of 5-bromodeoxyuridine (BrdUrd), and then irradiated with 313 nm light (a wavelength that selectively photolyzes DNA containing 5-bromouracil [BrUra]). Irradiation with 313 nm light induced breaks in the (3)H-labeled strands in cells grown with BrdUrd at a much higher frequency than in (14)C-labeled DNA of cells not exposed to BrdUrd. Breakage of the (3)H-labeled strands was about 0.6% as efficient as that of fully BrUra-substituted DNA. During growth in the presence of BrdUrd, susceptibility to 313 nm-induced breakage of the (3)H-labeled DNA strands increased, reaching a maximum in about one generation, and it decreased to zero during subsequent growth for one generation in medium containing dThd instead of BrdUrd. Heat denaturation of DNA extracted from dThd-(3)H-labeled cells grown in the presence of BrdUrd eliminated 313 nm-induced breakage of the (3)H-labeled strands. It is concluded that breakage of the (3)H-labeled DNA strands resulted from reaction with photoproducts in the base-paired, BrUra-containing strands, rather than from photolysis of BrdUrd incorporated into parental strands. It may be possible to utilize the phenomenon of interstrand breakage in physical studies of DNA replication.
流感嗜血杆菌用胸苷 -(3)H(dThd)标记,然后在5 - 溴脱氧尿苷(BrdUrd)存在下生长,接着用313 nm光(一种能选择性光解含5 - 溴尿嘧啶[BrUra]的DNA的波长)照射。用313 nm光照射时,在BrdUrd存在下生长的细胞中,(3)H标记链的断裂频率比未接触BrdUrd的细胞中(14)C标记的DNA高得多。(3)H标记链的断裂效率约为完全被BrUra取代的DNA的0.6%。在BrdUrd存在下生长期间,(3)H标记的DNA链对313 nm诱导断裂的敏感性增加,在大约一代时达到最大值,并且在随后用dThd而非BrdUrd的培养基中生长一代期间降至零。从在BrdUrd存在下生长的dThd -(3)H标记细胞中提取的DNA进行热变性消除了313 nm诱导的(3)H标记链的断裂。得出的结论是,(3)H标记的DNA链的断裂是由于与碱基配对的含BrUra链中的光产物反应,而不是由于掺入亲本链中的BrdUrd的光解。在DNA复制的物理研究中利用链间断裂现象可能是可行的。