Rubin E, Rumney S, Wang S, Kool E T
Department of Chemistry, University of Rochester, NY 14627, USA.
Nucleic Acids Res. 1995 Sep 11;23(17):3547-53. doi: 10.1093/nar/23.17.3547.
We report a novel convergent approach to the construction of circular DNA oligonucleotides from two smaller linear precursors. Circular DNAs 34-74 nucleotides (nt) in size are constructed non-enzymatically in a single step from two half-length oligomers. A DNA template is used to assemble the constituent parts into a triple helical complex which brings the four reactive ends together for chemical ligation with BrCN/imidazole/Ni2+. A homodimerization reaction strategy is successfully used on a small scale to construct circles 42, 58 and 74 nt in size. In addition, a heterodimerization strategy is successfully used in two cases to construct circular 34mers from different 16mer and 18mer precursors. Measurement of preparative yields for one biologically active 34mer circle shows that the dimerization strategy gives a yield higher than that from conventional cyclization and nearly as high as that for a normally synthesized linear DNA, establishing that there is not necessarily a yield penalty for circle construction. Six additional preparative circle constructions, giving conversions of approximately 33-85% from precursors to circular product, are also described. Convergent strategies allow the construction of medium and large size DNA molecules in higher yields than can be achieved by standard linear synthesis alone.
我们报道了一种从两个较小的线性前体构建环状DNA寡核苷酸的新型收敛方法。大小为34 - 74个核苷酸(nt)的环状DNA通过两个半长寡聚物在一步中无酶构建而成。使用DNA模板将组成部分组装成三螺旋复合物,该复合物将四个反应性末端聚集在一起,以便用溴化氰/咪唑/镍离子进行化学连接。同二聚化反应策略成功地在小规模上用于构建大小为42、58和74 nt的环。此外,异二聚化策略在两种情况下成功用于从不同的16聚体和18聚体前体构建环状34聚体。对一种生物活性34聚体环的制备产率的测量表明,二聚化策略的产率高于传统环化的产率,几乎与正常合成的线性DNA的产率一样高,这表明构建环不一定会导致产率损失。还描述了另外六种制备性环构建,从前体到环状产物的转化率约为33 - 85%。收敛策略允许以比单独的标准线性合成更高的产率构建中等和大尺寸的DNA分子。