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Creation of DNA overhangs by using modified DNA overhang cloning method

机译:使用修饰的DNA突出克隆克隆方法创建DNA突出端

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DNA overhang cloning (DOC) method was invented by Kevin A. Jarrell and colleagues to create DNA overhangs at the ends of polymerase chain reaction (PCR) fragments. To increase the ligation products of DOC and make it possible to join the ligation products together to yield a larger DNA fragment without amplification by using the secondary PCR, we modified the original method by lengthening RNA–DNA hybrids to 8 bp, using RNase H to digest RNA chains, and so on. We found that the ligation of PCR fragments with DNA overhangs could be improved significantly by using the modified DOC. The ligation products of the modified DOC were rich enough to be separated by using agarose gel and joined together to yield a larger DNA fragment without amplification by using the secondary PCR. The modified DOC is simpler and much more effective than the original one. The creation of DNA overhangs by using complementary DNA oligonucleotides, T4 ligase, and RNase H is simpler and cheaper than that by using reverse transcriptase and RNase H.
机译:Kevin A. Jarrell及其同事发明了DNA突出克隆(DOC)方法,以在聚合酶链反应(PCR)片段的末端创建DNA突出。为了增加DOC的连接产物并使通过第二次PCR无需扩增即可将连接产物连接在一起以产生更大的DNA片段,我们使用RNase H将RNA–DNA杂种延长至8 bp,从而对原始方法进行了改进消化RNA链等。我们发现,使用修饰的DOC可以显着改善PCR片段与DNA突出端的连接。修饰的DOC的连接产物足够丰富以至于可以通过使用琼脂糖凝胶分离并且结合在一起以产生更大的DNA片段而无需通过二次PCR进行扩增。修改后的DOC比原始DOC更简单,更有效。与使用逆转录酶和RNase H相比,使用互补DNA寡核苷酸,T4连接酶和RNase H产生DNA突出端更加简单和便宜。

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