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通过使用改良的DNA末端克隆方法创建DNA末端。

Creation of DNA overhangs by using modified DNA overhang cloning method.

作者信息

Li Wei, Gao Feng

机构信息

Laboratory of Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.

出版信息

Appl Microbiol Biotechnol. 2007 Jun;75(3):703-9. doi: 10.1007/s00253-007-0852-9. Epub 2007 Feb 17.

Abstract

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.

摘要

DNA 悬端克隆(DOC)方法由凯文·A·贾雷尔及其同事发明,用于在聚合酶链反应(PCR)片段末端创建 DNA 悬端。为了增加 DOC 的连接产物,并使其能够在不通过二次 PCR 扩增的情况下将连接产物连接在一起以产生更大的 DNA 片段,我们对原始方法进行了改进,将 RNA-DNA 杂交体延长至 8 个碱基对,使用核糖核酸酶 H 消化 RNA 链等。我们发现,使用改良的 DOC 可以显著提高带有 DNA 悬端的 PCR 片段的连接效率。改良 DOC 的连接产物足够丰富,可以通过琼脂糖凝胶分离,并在不通过二次 PCR 扩增的情况下连接在一起以产生更大的 DNA 片段。改良的 DOC 比原始方法更简单、更有效。使用互补 DNA 寡核苷酸、T4 连接酶和核糖核酸酶 H 创建 DNA 悬端比使用逆转录酶和核糖核酸酶 H 更简单、更便宜。

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