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利用 Surveyor 核酸内切酶纠正微芯片合成基因中的错误。

Error correction of microchip synthesized genes using Surveyor nuclease.

机构信息

Department of Biomedical Engineering, Duke University, Durham, NC27708, USA.

出版信息

Nucleic Acids Res. 2012 Feb;40(3):e23. doi: 10.1093/nar/gkr887. Epub 2011 Nov 29.

Abstract

The development of economical and high-throughput gene synthesis technology has been hampered by the high occurrence of errors in the synthesized products, which requires expensive labor and time to correct. Here, we describe an error correction reaction (ECR), which employs Surveyor, a mismatch-specific DNA endonuclease, to remove errors from synthetic genes. In ECR reactions, errors are revealed as mismatches by re-annealing of the synthetic gene products. Mismatches are recognized and excised by a combination of mismatch-specific endonuclease and 3'→5' exonuclease activities in the reaction mixture. Finally, overlap extension polymerase chain reaction (OE-PCR) re-assembles the resulting fragments into intact genes. The process can be iterated for increased fidelity. With two iterations, we were able to reduce errors in synthetic genes by >16-fold, yielding a final error rate of ∼1 in 8700  bp.

摘要

经济高效且高通量的基因合成技术的发展受到合成产物中高错误率的阻碍,这需要昂贵的劳动力和时间来纠正。在这里,我们描述了一种错误校正反应(ECR),它利用 Surveyor,一种错配特异性 DNA 内切酶,从合成基因中去除错误。在 ECR 反应中,通过重新退火合成基因产物,错误以错配的形式显现。错配被反应混合物中的错配特异性内切酶和 3'→5'外切酶活性识别并切除。最后,重叠延伸聚合酶链反应(OE-PCR)将产生的片段重新组装成完整的基因。该过程可以通过迭代进行,以提高保真度。通过两次迭代,我们能够将合成基因中的错误减少 16 倍以上,最终的错误率约为每 8700 bp 出现 1 个错误。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1980/3273826/43afbcb5030a/gkr887f1.jpg

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