Zhang K, Taylor J S
Department of Chemistry, Washington University, St. Louis, Missouri 63130, USA.
Biochemistry. 2001 Jan 9;40(1):153-9. doi: 10.1021/bi001781j.
DNA strand breaks are produced by a variety of agents and processes such as ionizing radiation, xenobiotics, oxidative metabolism, and enzymatic processing of DNA base damage. One of the major types of strand breaks produced by these processes is a single nucleotide gap terminating in 5'- and 3'-phosphates. Previously, we had developed a method for sequence-specifically producing such phosphate-terminated strand breaks in an oligodeoxynucleotide by way of two photochemically activated (caged) building blocks placed in tandem. We now report the design and synthesis of a single caged building block consisting of 1,3-(2-nitrophenyl)-1,3-propanediol, for producing phosphate-terminated strand breaks, and its use producing such a break at a specific site in a double-stranded circular DNA vector. To produce the site-specific break in a duplex vector, a primer containing the caged single strand break was extended opposite the single strand form of a circular DNA vector followed by enzymatic ligation and purification. The single strand break could then be formed in quantitative yield by irradiation of the vector with 365 nm light. In contrast to a previous study, it was found that the strand break can be repaired by Escherichia coli DNA polymerase I and E. coli DNA ligase alone, though less efficiently than in the presence of the 3'-phosphate processing enzyme E. coli endonuclease IV. Repair in the absence of endonuclease IV could be attributed to hydrolysis of the 3'-phosphate in the presence of dNTP and to a lesser extent to exonucleolytic removal of the 3'-phosphate-bearing terminal nucleotide by way of the 3' --> 5' exonuclease activity of polymerase I. This work demonstrates that specialized 3'-end processing enzymes such as endonuclease IV or exonuclease III are not absolutely required for repair of phosphate-terminated gaps. In addition to preparing single strand breaks, the caged building block described should also be useful for preparing double strand breaks and multiply damaged sites that might otherwise be difficult to prepare by other methods due to their lability.
DNA链断裂可由多种因素和过程产生,如电离辐射、外源性物质、氧化代谢以及DNA碱基损伤的酶促处理。这些过程产生的主要链断裂类型之一是一个以5'-和3'-磷酸为末端的单核苷酸缺口。此前,我们开发了一种方法,通过串联放置两个光化学活化(笼蔽)的构建模块,在寡脱氧核苷酸中序列特异性地产生这种磷酸化末端的链断裂。我们现在报告一种由1,3-(2-硝基苯基)-1,3-丙二醇组成的单个笼蔽构建模块的设计与合成,用于产生磷酸化末端的链断裂,以及其在双链环状DNA载体的特定位点产生这种断裂的应用。为了在双链载体中产生位点特异性断裂,含有笼蔽单链断裂的引物与环状DNA载体的单链形式相对延伸,随后进行酶促连接和纯化。然后通过用365 nm光照射载体,以定量产率形成单链断裂。与先前的研究相比,发现仅大肠杆菌DNA聚合酶I和大肠杆菌DNA连接酶就能修复链断裂,尽管效率低于存在3'-磷酸处理酶大肠杆菌内切核酸酶IV时。在没有内切核酸酶IV的情况下进行修复可归因于在dNTP存在下3'-磷酸的水解,以及在较小程度上归因于通过聚合酶I的3'→5'外切核酸酶活性对外切3'-磷酸的末端核苷酸进行外切核酸酶去除。这项工作表明,修复磷酸化末端缺口并不绝对需要像内切核酸酶IV或外切核酸酶III这样的专门3'-末端处理酶。除了制备单链断裂外,所述的笼蔽构建模块还应可用于制备双链断裂和多重损伤位点,否则由于其不稳定性,可能难以通过其他方法制备。